Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23382 |
|---|---|
| ensemblid | ENSG00000158467.17 |
| hgncid | 22204 |
| symbol | AHCYL2 |
| name | adenosylhomocysteinase like 2 |
| refseq_nuc | NM_015328.4 |
| refseq_prot | NP_056143.1 |
| ensembl_nuc | ENST00000325006.8 |
| ensembl_prot | ENSP00000315931.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 129225030 |
| end | 129430211 |
| strand | + |
| ver | v1.2 |
| region | chr7:129225030-129430211 |
| region5000 | chr7:129220030-129435211 |
| regionname0 | AHCYL2_chr7_129225030_129430211 |
| regionname5000 | AHCYL2_chr7_129220030_129435211 |
| 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 | 611 | 290 | 80 | 60 | 102 | 12 | 34 | 82 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0002 | 0/0 | 611 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0003 | 0/0 | 611 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| 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 | 1/0 | 1836 | 199 | 56 | 42 | 67 | 8 | 25 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| c0002 | 0/1 | 1836 | 90 | 23 | 18 | 35 | 4 | 9 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| c0003 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| c0004 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| c0005 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| 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 | 0/1 | 3214 | 88 | 16 | 18 | 39 | 6 | 8 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0002 | 1/0 | 3214 | 75 | 25 | 21 | 16 | 2 | 10 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0003 | 0/0 | 3214 | 67 | 3 | 11 | 40 | 3 | 10 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0004 | 0/0 | 3214 | 9 | 1 | 2 | 3 | 0 | 3 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0005 | 0/0 | 3212 | 7 | 7 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0006 | 0/0 | 3214 | 6 | 6 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0007 | 0/0 | 3214 | 4 | 3 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0008 | 0/0 | 3214 | 3 | 0 | 0 | 3 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0009 | 0/0 | 3214 | 3 | 0 | 2 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0010 | 0/0 | 3214 | 3 | 0 | 0 | 0 | 0 | 3 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0011 | 0/0 | 3214 | 3 | 0 | 2 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0012 | 0/0 | 3216 | 3 | 2 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0013 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0014 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0015 | 0/0 | 3212 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0016 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0017 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0018 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0019 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0020 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0021 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0022 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0023 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0024 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0025 | 0/0 | 3214 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0026 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| t0027 | 0/0 | 3212 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| 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 | 1/0 | 1836 | 199 | 56 | 42 | 67 | 8 | 25 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002 | 0/1 | 1836 | 90 | 23 | 18 | 35 | 4 | 9 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0005 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0002c0003 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0003c0004 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5049 | 78 | 13 | 14 | 39 | 5 | 7 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0002 | 1/0 | 5049 | 49 | 9 | 18 | 13 | 1 | 7 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0003 | 0/0 | 5049 | 17 | 1 | 0 | 9 | 1 | 6 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0004 | 0/0 | 5049 | 8 | 1 | 2 | 2 | 0 | 3 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0005 | 0/0 | 5047 | 7 | 7 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0006 | 0/0 | 5049 | 5 | 5 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0007 | 0/0 | 5049 | 4 | 3 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0008 | 0/0 | 5049 | 3 | 0 | 0 | 3 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0009 | 0/0 | 5049 | 3 | 0 | 2 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0011 | 0/0 | 5049 | 3 | 0 | 2 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0012 | 0/0 | 5051 | 3 | 2 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0013 | 0/0 | 5051 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0014 | 0/0 | 5049 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0015 | 0/0 | 5047 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0016 | 0/0 | 5051 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0017 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0018 | 0/0 | 5049 | 2 | 2 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0019 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0020 | 0/0 | 5049 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0021 | 0/0 | 5051 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0022 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0023 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0025 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0026 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0001t0027 | 0/0 | 5047 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0001 | 0/1 | 5049 | 9 | 3 | 4 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0002 | 0/0 | 5049 | 25 | 16 | 3 | 3 | 1 | 2 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0003 | 0/0 | 5049 | 50 | 2 | 11 | 31 | 2 | 4 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0004 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0006 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0010 | 0/0 | 5049 | 3 | 0 | 0 | 0 | 0 | 3 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0002t0017 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0001c0005t0024 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0002c0003t0002 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| a0003c0004t0001 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | copy fasta | chr7 | 129220030 | 129435211 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0011g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0018g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0019g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0020g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0021g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0023g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0025g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0026g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0001t0027g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0010g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0010g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0002t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0001c0005t0024g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0002c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0270 | EUR | GBR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | GBR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0135 | EUR | GBR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0231 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0236 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00673 | hp2 | a0001 | c0001 | t0019 | g0155 | EAS | CHS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0261 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0225 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0264 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0161 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0287 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0090 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0120 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0209 | EUR | IBS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0212 | EUR | IBS | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0283 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0214 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0205 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0259 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0131 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0266 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | CDX | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02258 | hp1 | a0001 | c0001 | t0014 | g0067 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0213 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02273 | hp2 | a0001 | c0001 | t0011 | g0033 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0245 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0246 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | KHV | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0165 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0288 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02622 | hp1 | a0001 | c0002 | t0017 | g0253 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0249 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0066 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02683 | hp2 | a0001 | c0002 | t0010 | g0274 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0050 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02723 | hp1 | a0001 | c0001 | t0023 | g0095 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0078 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02886 | hp2 | a0001 | c0005 | t0024 | g0113 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0121 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0132 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0114 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03098 | hp1 | a0001 | c0001 | t0027 | g0045 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0118 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0219 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0285 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03239 | hp2 | a0002 | c0003 | t0002 | g0199 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0119 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03491 | hp1 | a0003 | c0004 | t0001 | g0042 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0257 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0192 | AFR | ESN | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03579 | hp2 | a0001 | c0001 | t0026 | g0152 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0197 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0144 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0256 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0290 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04184 | hp1 | a0001 | c0002 | t0010 | g0273 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0252 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04199 | hp2 | a0001 | c0001 | t0025 | g0082 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04204 | hp1 | a0001 | c0002 | t0010 | g0275 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | STU | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0222 | EAS | CHB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | YRI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18974 | hp1 | a0001 | c0001 | t0008 | g0150 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0184 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0277 | AFR | LWK | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | LWK | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0223 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0284 | AFR | ASW | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ASW | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0089 | EUR | TSI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0228 | EUR | TSI | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01123 | hp1 | a0001 | c0001 | t0021 | g0092 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0291 | AMR | CLM | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ACB | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0258 | AFR | USA | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0077 | AFR | USA | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | USA | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0271 | AFR | USA | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | LWK | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0196 | REF | REF | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0125 | REF | REF | AHCYL2_chr7_129220030_129435211 | AHCYL2 | chr7 | 129220030 | 129435211 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129225252
|
G | C | 1 | a0002 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.176G>C | p.Arg59Pro | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/17 | 223/5049 | 176/1836 | 59/611 | chr7 | 129225252 | ||
| chr7:129225410
|
G | A | 1 | a0003 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.334G>A | p.Val112Ile | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/17 | 381/5049 | 334/1836 | 112/611 | chr7 | 129225410 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129225289
|
C | T | 2 | a0001c0002a0002c0003 | 91 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
synonymous_variant | LOW | c.213C>T | p.Ala71Ala | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/17 | 260/5049 | 213/1836 | 71/611 | chr7 | 129225289 | ||
| chr7:129426552
|
T | G | 1 | a0001c0005 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1818T>G | p.Pro606Pro | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/17 | 1865/5049 | 1818/1836 | 606/611 | chr7 | 129426552 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129427212
|
T | C | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(4): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 167 | chr7 | 129427212 | |||||
| chr7:129427958
|
G | A | 2 | a0001c0001t0009a0001c0002t0010 | 6 | HG01257.hp2 HG01496.hp1 HG02683.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*913G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 913 | chr7 | 129427958 | |||||
| chr7:129428004
|
G | A | 1 | a0001c0001t0011 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 959 | chr7 | 129428004 | |||||
| chr7:129428099
|
C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1054 | chr7 | 129428099 | |||||
| chr7:129428184
|
C | T | 4 | a0001c0001t0006a0001c0001t0026a0001c0001t0027others(1): Show | 8 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1139C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1139 | chr7 | 129428184 | |||||
| chr7:129428185
|
A | G | 1 | a0001c0001t0027 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1140 | chr7 | 129428185 | |||||
| chr7:129428232
|
A | G | 1 | a0001c0001t0025 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1187 | chr7 | 129428232 | |||||
| chr7:129428306
|
A | G | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(4): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1261A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1261 | chr7 | 129428306 | |||||
| chr7:129428465
|
G | T | 1 | a0001c0005t0024 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1420G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1420 | chr7 | 129428465 | |||||
| chr7:129428733
|
C | T | 1 | a0001c0001t0026 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 1688 | chr7 | 129428733 | |||||
| chr7:129429060
|
C | T | 1 | a0001c0001t0018 | 2 | HG01891.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2015C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2015 | chr7 | 129429060 | |||||
| chr7:129429079
|
G | T | 1 | a0001c0001t0011 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2034 | chr7 | 129429079 | |||||
| chr7:129429137
|
G | A | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(14): Show | 124 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2092G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2092 | chr7 | 129429137 | |||||
| chr7:129429175
|
A | C | 2 | a0001c0001t0007a0001c0001t0027 | 5 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2130A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2130 | chr7 | 129429175 | |||||
| chr7:129429212
|
A | C | 4 | a0001c0001t0014a0001c0001t0015a0001c0001t0017others(1): Show | 6 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2167A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2167 | chr7 | 129429212 | |||||
| chr7:129429348
|
C | T | 3 | a0001c0001t0006a0001c0001t0026a0001c0002t0006 | 7 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2303C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2303 | chr7 | 129429348 | |||||
| chr7:129429870
|
G | T | 2 | a0001c0001t0008a0001c0001t0019 | 4 | HG00673.hp2 NA18974.hp1 NA18977.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2825G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2825 | chr7 | 129429870 | |||||
| chr7:129429959
|
C | T | 1 | a0001c0001t0013 | 2 | HG03139.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2914C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2914 | chr7 | 129429959 | |||||
| chr7:129430011
|
C | G | 1 | a0001c0001t0022 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2966C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2966 | chr7 | 129430011 | |||||
| chr7:129430020
|
C | CAT | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0016others(3): Show | 10 | HG01123.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2990_*2991dupAT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2992 | INFO_REALIGN_3_PRIME | chr7 | 129430020 | ||||
| chr7:129430020
|
CAT | C | 3 | a0001c0001t0005a0001c0001t0015a0001c0001t0027 | 10 | HG02257.hp1 HG02451.hp2 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2990_*2991delAT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2990 | INFO_REALIGN_3_PRIME | chr7 | 129430020 | ||||
| chr7:129430037
|
C | A | 4 | a0001c0001t0012a0001c0001t0013a0001c0001t0016others(1): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2992C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 17/17 | 2992 | chr7 | 129430037 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129225515
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+76C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225515 | ||||||
| chr7:129225529
|
C | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+90C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225529 | ||||||
| chr7:129225752
|
G | A | 1 | a0001c0002t0002g0001 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.363+313G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225752 | ||||||
| chr7:129225830
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363+391A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225830 | ||||||
| chr7:129225908
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+469G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225908 | ||||||
| chr7:129225928
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+489C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129225928 | ||||||
| chr7:129226015
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+576C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226015 | ||||||
| chr7:129226101
|
C | T | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.363+662C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226101 | ||||||
| chr7:129226272
|
A | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.363+833A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226272 | ||||||
| chr7:129226288
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG00673.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+849G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226288 | ||||||
| chr7:129226511
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.363+1072G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226511 | ||||||
| chr7:129226548
|
G | T | 91 | a0001c0002t0001g0190a0001c0002t0001g0196a0001c0002t0001g0203others(88): Show | 91 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.363+1109G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226548 | ||||||
| chr7:129226612
|
T | G | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+1173T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226612 | ||||||
| chr7:129226750
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+1311A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226750 | ||||||
| chr7:129226775
|
A | C | 147 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.363+1336A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226775 | ||||||
| chr7:129226848
|
G | A | 1 | a0001c0002t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.363+1409G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226848 | ||||||
| chr7:129226922
|
A | AACTT | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+1483_363+1484i others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226922 | ||||||
| chr7:129226932
|
C | A | 3 | a0001c0001t0003g0135a0001c0001t0004g0136a0001c0001t0004g0137 | 3 | HG00140.hp1 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+1493C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129226932 | ||||||
| chr7:129227109
|
C | G | 91 | a0001c0002t0001g0190a0001c0002t0001g0196a0001c0002t0001g0203others(88): Show | 91 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.363+1670C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227109 | ||||||
| chr7:129227112
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+1673T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227112 | ||||||
| chr7:129227287
|
C | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.363+1848C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227287 | ||||||
| chr7:129227429
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.363+1990C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227429 | ||||||
| chr7:129227457
|
CA | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0052others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+2038delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129227457 | |||||
| chr7:129227482
|
C | T | 1 | a0001c0001t0007g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.363+2043C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227482 | ||||||
| chr7:129227608
|
C | CA | 14 | a0001c0001t0001g0115a0001c0001t0006g0116a0001c0001t0006g0117others(11): Show | 14 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+2193dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129227608 | |||||
| chr7:129227608
|
CA | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(64): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.363+2193delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129227608 | |||||
| chr7:129227608
|
CAA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.363+2192_363+2193d others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129227608 | |||||
| chr7:129227709
|
C | T | 1 | a0001c0002t0002g0276 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.363+2270C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227709 | ||||||
| chr7:129227895
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.363+2456C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227895 | ||||||
| chr7:129227928
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+2489G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129227928 | ||||||
| chr7:129228093
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+2654T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228093 | ||||||
| chr7:129228150
|
T | C | 5 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(2): Show | 5 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+2711T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228150 | ||||||
| chr7:129228267
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+2828C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228267 | ||||||
| chr7:129228318
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.363+2879G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228318 | ||||||
| chr7:129228396
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.363+2957A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228396 | ||||||
| chr7:129228449
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+3010G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228449 | ||||||
| chr7:129228815
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+3376C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129228815 | ||||||
| chr7:129229018
|
G | A | 2 | a0001c0002t0002g0200a0002c0003t0002g0199 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.363+3579G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229018 | ||||||
| chr7:129229061
|
CTTTTTTT others(3): Show |
C | 261 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.363+3636_363+3645d others(12): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129229061 | |||||
| chr7:129229061
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0055a0001c0001t0002g0054a0001c0002t0002g0191 | 3 | HG03195.hp2 NA18942.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.363+3635_363+3645d others(13): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129229061 | |||||
| chr7:129229143
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.363+3704C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229143 | ||||||
| chr7:129229294
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+3855C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229294 | ||||||
| chr7:129229509
|
C | CAA | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+4071_363+4072i others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129229509 | |||||
| chr7:129229538
|
C | T | 3 | a0001c0002t0010g0273a0001c0002t0010g0274a0001c0002t0010g0275 | 3 | HG02683.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.363+4099C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229538 | ||||||
| chr7:129229808
|
A | G | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+4369A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229808 | ||||||
| chr7:129229870
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+4431A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229870 | ||||||
| chr7:129229877
|
A | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+4438A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129229877 | ||||||
| chr7:129230008
|
A | G | 1 | a0001c0002t0003g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.363+4569A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230008 | ||||||
| chr7:129230061
|
A | G | 2 | a0001c0002t0002g0188a0001c0002t0002g0198 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.363+4622A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230061 | ||||||
| chr7:129230069
|
T | C | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.363+4630T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230069 | ||||||
| chr7:129230079
|
C | CT | 20 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0111others(17): Show | 20 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.363+4663dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129230079 | |||||
| chr7:129230079
|
CT | C | 10 | a0001c0001t0001g0140a0001c0001t0002g0008a0001c0001t0002g0054others(7): Show | 10 | HG00140.hp2 HG01167.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+4663delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129230079 | |||||
| chr7:129230092
|
T | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+4653T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230092 | ||||||
| chr7:129230325
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.363+4886A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230325 | ||||||
| chr7:129230400
|
G | A | 4 | a0001c0001t0003g0135a0001c0001t0004g0136a0001c0001t0004g0137others(1): Show | 4 | HG00140.hp1 HG01346.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+4961G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230400 | ||||||
| chr7:129230463
|
G | T | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.363+5024G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230463 | ||||||
| chr7:129230484
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+5045G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230484 | ||||||
| chr7:129230547
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0053 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.363+5108C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230547 | ||||||
| chr7:129230573
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.363+5134C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230573 | ||||||
| chr7:129230654
|
C | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.363+5215C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230654 | ||||||
| chr7:129230698
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.363+5259G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230698 | ||||||
| chr7:129230704
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.363+5265C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230704 | ||||||
| chr7:129230729
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+5290C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230729 | ||||||
| chr7:129230806
|
C | T | 3 | a0001c0002t0001g0263a0001c0002t0003g0197a0001c0002t0003g0264 | 3 | HG00741.hp2 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.363+5367C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230806 | ||||||
| chr7:129230807
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.363+5368G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129230807 | ||||||
| chr7:129231165
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+5726G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231165 | ||||||
| chr7:129231217
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.363+5778C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231217 | ||||||
| chr7:129231259
|
C | A | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+5820C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231259 | ||||||
| chr7:129231318
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+5879C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231318 | ||||||
| chr7:129231610
|
A | T | 1 | a0001c0002t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.363+6171A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231610 | ||||||
| chr7:129231691
|
A | G | 147 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.363+6252A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231691 | ||||||
| chr7:129231842
|
G | C | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+6403G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231842 | ||||||
| chr7:129231872
|
C | T | 91 | a0001c0002t0001g0190a0001c0002t0001g0196a0001c0002t0001g0203others(88): Show | 91 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.363+6433C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231872 | ||||||
| chr7:129231924
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.363+6485G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129231924 | ||||||
| chr7:129232039
|
T | A | 2 | a0001c0001t0014g0067a0001c0001t0017g0066 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.363+6600T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129232039 | ||||||
| chr7:129232057
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+6618G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129232057 | ||||||
| chr7:129232181
|
C | G | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+6742C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129232181 | ||||||
| chr7:129232976
|
C | T | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+7537C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129232976 | ||||||
| chr7:129233066
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+7627G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233066 | ||||||
| chr7:129233121
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.363+7682A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233121 | ||||||
| chr7:129233139
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+7700G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233139 | ||||||
| chr7:129233389
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.363+7950C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233389 | ||||||
| chr7:129233462
|
C | T | 1 | a0001c0002t0003g0259 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.363+8023C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233462 | ||||||
| chr7:129233584
|
T | G | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.363+8145T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233584 | ||||||
| chr7:129233665
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+8226G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233665 | ||||||
| chr7:129233680
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.363+8241G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233680 | ||||||
| chr7:129233838
|
G | A | 147 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.363+8399G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233838 | ||||||
| chr7:129233984
|
T | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.363+8545T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129233984 | ||||||
| chr7:129234039
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+8600T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234039 | ||||||
| chr7:129234227
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+8788G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234227 | ||||||
| chr7:129234287
|
C | T | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.363+8848C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234287 | ||||||
| chr7:129234371
|
A | G | 1 | a0001c0001t0008g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.363+8932A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234371 | ||||||
| chr7:129234460
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+9021G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234460 | ||||||
| chr7:129234555
|
T | G | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.363+9116T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129234555 | ||||||
| chr7:129235280
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+9841C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235280 | ||||||
| chr7:129235306
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.363+9867C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235306 | ||||||
| chr7:129235417
|
ATTC | A | 54 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+9993_363+9995d others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129235417 | |||||
| chr7:129235620
|
G | A | 2 | a0001c0001t0002g0153a0001c0001t0002g0185 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+10181G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235620 | ||||||
| chr7:129235708
|
C | A | 2 | a0001c0002t0003g0206a0001c0002t0003g0207 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.363+10269C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235708 | ||||||
| chr7:129235746
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+10307G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235746 | ||||||
| chr7:129235760
|
C | T | 2 | a0001c0002t0003g0257a0001c0002t0003g0258 | 2 | HG03491.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.363+10321C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235760 | ||||||
| chr7:129235771
|
C | G | 147 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.363+10332C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235771 | ||||||
| chr7:129235796
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+10357C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235796 | ||||||
| chr7:129235943
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+10504C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129235943 | ||||||
| chr7:129236020
|
C | CT | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG01081.hp1 HG01167.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+10599dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129236020 | |||||
| chr7:129236156
|
G | A | 28 | a0001c0001t0003g0135a0001c0001t0003g0139a0001c0001t0003g0142others(25): Show | 28 | HG00140.hp1 HG00673.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.363+10717G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236156 | ||||||
| chr7:129236172
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+10733G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236172 | ||||||
| chr7:129236290
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+10851T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236290 | ||||||
| chr7:129236389
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.363+10950C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236389 | ||||||
| chr7:129236609
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.363+11170A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236609 | ||||||
| chr7:129236662
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+11223C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236662 | ||||||
| chr7:129236684
|
TACATATC others(17): Show |
T | 1 | a0001c0002t0003g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.363+11249_363+1127 others(28): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129236684 | |||||
| chr7:129236808
|
G | C | 54 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+11369G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129236808 | ||||||
| chr7:129237142
|
G | C | 1 | a0001c0002t0003g0209 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.363+11703G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237142 | ||||||
| chr7:129237464
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+12025T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237464 | ||||||
| chr7:129237556
|
AT | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.363+12129delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129237556 | |||||
| chr7:129237556
|
ATT | A | 11 | a0001c0001t0001g0292a0001c0001t0003g0154a0001c0001t0014g0068others(8): Show | 11 | HG01516.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+12128_363+1212 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129237556 | |||||
| chr7:129237597
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363+12158G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237597 | ||||||
| chr7:129237603
|
T | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+12164T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237603 | ||||||
| chr7:129237613
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.363+12174A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237613 | ||||||
| chr7:129237636
|
A | G | 2 | a0001c0001t0013g0118a0001c0001t0013g0119 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.363+12197A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237636 | ||||||
| chr7:129237847
|
G | A | 22 | a0001c0001t0003g0139a0001c0001t0003g0142a0001c0001t0003g0143others(19): Show | 22 | HG00673.hp2 HG01081.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.363+12408G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237847 | ||||||
| chr7:129237889
|
T | C | 2 | a0001c0002t0003g0213a0001c0002t0003g0214 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.363+12450T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237889 | ||||||
| chr7:129237941
|
T | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+12502T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129237941 | ||||||
| chr7:129238515
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.363+13076C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238515 | ||||||
| chr7:129238516
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.363+13077C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238516 | ||||||
| chr7:129238635
|
A | G | 3 | a0001c0001t0001g0292a0001c0001t0018g0283a0001c0001t0018g0284 | 3 | HG01891.hp1 HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+13196A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238635 | ||||||
| chr7:129238644
|
G | GT | 4 | a0001c0001t0012g0114a0001c0001t0012g0131a0001c0001t0016g0121others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+13208dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129238644 | |||||
| chr7:129238747
|
T | TTGAAACT others(16): Show |
1 | a0001c0002t0003g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.363+13315_363+1333 others(27): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129238747 | |||||
| chr7:129238815
|
G | C | 3 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287 | 3 | HG01099.hp1 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.363+13376G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238815 | ||||||
| chr7:129238838
|
A | T | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.363+13399A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238838 | ||||||
| chr7:129238912
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+13473A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238912 | ||||||
| chr7:129238913
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0002g0009 | 2 | NA18982.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.363+13474C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238913 | ||||||
| chr7:129238959
|
A | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+13520A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129238959 | ||||||
| chr7:129239024
|
CAG | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+13586_363+1358 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239024 | ||||||
| chr7:129239029
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+13590A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239029 | ||||||
| chr7:129239050
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+13611G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239050 | ||||||
| chr7:129239342
|
A | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+13903A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239342 | ||||||
| chr7:129239357
|
T | G | 1 | a0001c0001t0002g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.363+13918T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239357 | ||||||
| chr7:129239452
|
T | C | 1 | a0001c0002t0002g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.363+14013T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239452 | ||||||
| chr7:129239506
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+14067G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239506 | ||||||
| chr7:129239537
|
G | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+14098G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239537 | ||||||
| chr7:129239637
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0102 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.363+14198C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239637 | ||||||
| chr7:129239768
|
A | G | 1 | a0001c0002t0003g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.363+14329A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239768 | ||||||
| chr7:129239786
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.363+14347C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239786 | ||||||
| chr7:129239837
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+14398C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239837 | ||||||
| chr7:129239869
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+14430A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239869 | ||||||
| chr7:129239921
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+14482C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239921 | ||||||
| chr7:129239949
|
C | T | 54 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+14510C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239949 | ||||||
| chr7:129239961
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+14522C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129239961 | ||||||
| chr7:129240057
|
C | G | 1 | a0001c0001t0012g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.363+14618C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240057 | ||||||
| chr7:129240169
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+14730C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240169 | ||||||
| chr7:129240227
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.363+14788A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240227 | ||||||
| chr7:129240229
|
A | AAGAG | 9 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(6): Show | 9 | HG01099.hp1 HG01123.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+14793_363+1479 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129240229 | |||||
| chr7:129240229
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.363+14790A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240229 | ||||||
| chr7:129240311
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.363+14872C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240311 | ||||||
| chr7:129240420
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.363+14981A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240420 | ||||||
| chr7:129240543
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+15104A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240543 | ||||||
| chr7:129240648
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+15209T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240648 | ||||||
| chr7:129240648
|
T | G | 54 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+15209T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240648 | ||||||
| chr7:129240856
|
A | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0215 | 2 | HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.363+15417A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240856 | ||||||
| chr7:129240910
|
G | A | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+15471G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240910 | ||||||
| chr7:129240990
|
G | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+15551G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129240990 | ||||||
| chr7:129241356
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+15917T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241356 | ||||||
| chr7:129241483
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.363+16044C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241483 | ||||||
| chr7:129241553
|
G | C | 5 | a0001c0002t0001g0203a0001c0002t0002g0192a0001c0002t0002g0216others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+16114G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241553 | ||||||
| chr7:129241621
|
T | C | 2 | a0001c0002t0003g0193a0001c0002t0003g0266 | 2 | HG02074.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.363+16182T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241621 | ||||||
| chr7:129241691
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+16252A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241691 | ||||||
| chr7:129241885
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.363+16446A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241885 | ||||||
| chr7:129241916
|
C | T | 1 | a0001c0002t0002g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.363+16477C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129241916 | ||||||
| chr7:129242292
|
C | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+16853C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242292 | ||||||
| chr7:129242378
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+16939A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242378 | ||||||
| chr7:129242455
|
C | T | 16 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0134others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+17016C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242455 | ||||||
| chr7:129242487
|
G | C | 3 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287 | 3 | HG01099.hp1 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.363+17048G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242487 | ||||||
| chr7:129242531
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(234): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.363+17092T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242531 | ||||||
| chr7:129242586
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.363+17147G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242586 | ||||||
| chr7:129242619
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+17180A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242619 | ||||||
| chr7:129242705
|
G | A | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0183 | 3 | HG01069.hp2 HG02683.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.363+17266G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242705 | ||||||
| chr7:129242717
|
G | GA | 6 | a0001c0001t0001g0055a0001c0001t0002g0010a0001c0001t0002g0070others(3): Show | 6 | HG00597.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+17295dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129242717 | |||||
| chr7:129242751
|
A | C | 115 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.363+17312A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242751 | ||||||
| chr7:129242893
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.363+17454C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129242893 | ||||||
| chr7:129243018
|
C | CT | 18 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(15): Show | 18 | HG00597.hp2 HG01099.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.363+17599dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129243018 | |||||
| chr7:129243166
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+17727G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243166 | ||||||
| chr7:129243430
|
T | G | 1 | a0001c0002t0003g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.363+17991T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243430 | ||||||
| chr7:129243456
|
C | A | 1 | a0001c0001t0019g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.363+18017C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243456 | ||||||
| chr7:129243558
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+18119T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243558 | ||||||
| chr7:129243564
|
GTTTGTT | G | 108 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.363+18140_363+1814 others(10): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129243564 | |||||
| chr7:129243605
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.363+18166G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243605 | ||||||
| chr7:129243623
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+18184C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243623 | ||||||
| chr7:129243827
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+18388T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129243827 | ||||||
| chr7:129243953
|
C | CTTATT | 5 | a0001c0001t0001g0140a0001c0002t0001g0267a0001c0002t0001g0269others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+18536_363+1854 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129243953 | |||||
| chr7:129243953
|
CTTATTTT others(3): Show |
C | 4 | a0001c0001t0001g0138a0001c0001t0002g0047a0001c0001t0002g0053others(1): Show | 4 | HG00741.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+18531_363+1854 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129243953 | |||||
| chr7:129244021
|
C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0065others(4): Show | 7 | NA18946.hp2 NA18950.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+18582C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244021 | ||||||
| chr7:129244135
|
A | G | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+18696A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244135 | ||||||
| chr7:129244185
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+18746G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244185 | ||||||
| chr7:129244216
|
A | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 112 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+18777A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244216 | ||||||
| chr7:129244259
|
C | T | 1 | a0001c0001t0006g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+18820C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244259 | ||||||
| chr7:129244437
|
G | C | 55 | a0001c0002t0001g0263a0001c0002t0002g0001a0001c0002t0002g0188others(52): Show | 55 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.363+18998G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244437 | ||||||
| chr7:129244446
|
G | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.363+19007G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244446 | ||||||
| chr7:129244536
|
C | G | 1 | a0001c0001t0004g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.363+19097C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244536 | ||||||
| chr7:129244966
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+19527G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244966 | ||||||
| chr7:129244974
|
A | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+19535A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244974 | ||||||
| chr7:129244994
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+19555A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129244994 | ||||||
| chr7:129245025
|
CT | C | 146 | a0001c0001t0001g0122a0001c0001t0001g0138a0001c0001t0001g0140others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.363+19605delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129245025 | |||||
| chr7:129245156
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.363+19717C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245156 | ||||||
| chr7:129245185
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+19746T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245185 | ||||||
| chr7:129245377
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+19938A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245377 | ||||||
| chr7:129245466
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+20027C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245466 | ||||||
| chr7:129245581
|
C | T | 1 | a0001c0001t0008g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.363+20142C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245581 | ||||||
| chr7:129245582
|
T | TTA | 109 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.363+20148_363+2014 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129245582 | |||||
| chr7:129245726
|
G | A | 1 | a0001c0002t0003g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.363+20287G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245726 | ||||||
| chr7:129245929
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 112 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+20490C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245929 | ||||||
| chr7:129245951
|
G | A | 4 | a0001c0001t0012g0114a0001c0001t0012g0131a0001c0001t0016g0121others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+20512G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129245951 | ||||||
| chr7:129246002
|
C | A | 1 | a0001c0001t0002g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.363+20563C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246002 | ||||||
| chr7:129246015
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+20576G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246015 | ||||||
| chr7:129246035
|
C | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+20596C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246035 | ||||||
| chr7:129246062
|
G | GT | 8 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01123.hp2 HG02886.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+20637dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129246062 | |||||
| chr7:129246643
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+21204C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246643 | ||||||
| chr7:129246644
|
G | T | 1 | a0001c0001t0002g0006 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.363+21205G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246644 | ||||||
| chr7:129246662
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+21223A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246662 | ||||||
| chr7:129246695
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363+21256T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246695 | ||||||
| chr7:129246734
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+21295T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246734 | ||||||
| chr7:129246841
|
T | G | 2 | a0001c0001t0014g0067a0001c0001t0017g0066 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.363+21402T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246841 | ||||||
| chr7:129246980
|
T | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.363+21541T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129246980 | ||||||
| chr7:129247216
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.363+21777T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247216 | ||||||
| chr7:129247267
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.363+21828G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247267 | ||||||
| chr7:129247272
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.363+21833A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247272 | ||||||
| chr7:129247395
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+21956C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247395 | ||||||
| chr7:129247404
|
A | G | 3 | a0001c0001t0003g0145a0001c0001t0004g0144a0001c0001t0004g0166 | 3 | HG03831.hp1 NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.363+21965A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247404 | ||||||
| chr7:129247603
|
C | CT | 266 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.363+22173dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129247603 | |||||
| chr7:129247612
|
T | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+22173T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247612 | ||||||
| chr7:129247660
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+22221G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247660 | ||||||
| chr7:129247891
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.363+22452T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247891 | ||||||
| chr7:129247894
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.363+22455A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129247894 | ||||||
| chr7:129248084
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 110 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.363+22645A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248084 | ||||||
| chr7:129248163
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+22724G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248163 | ||||||
| chr7:129248242
|
A | G | 1 | a0001c0002t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.363+22803A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248242 | ||||||
| chr7:129248276
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.363+22837C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248276 | ||||||
| chr7:129248510
|
CT | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.363+23083delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129248510 | |||||
| chr7:129248522
|
T | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0021 | 2 | HG01167.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.363+23083T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248522 | ||||||
| chr7:129248571
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.363+23132G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248571 | ||||||
| chr7:129248613
|
G | A | 1 | a0001c0002t0003g0220 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.363+23174G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248613 | ||||||
| chr7:129248620
|
AT | A | 17 | a0001c0001t0001g0292a0001c0001t0002g0003a0001c0001t0002g0004others(14): Show | 17 | HG00099.hp1 HG00673.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.363+23196delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129248620 | |||||
| chr7:129248703
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+23264T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248703 | ||||||
| chr7:129248809
|
T | C | 1 | a0001c0001t0007g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.363+23370T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129248809 | ||||||
| chr7:129248996
|
C | CT | 146 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0038others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.363+23575dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129248996 | |||||
| chr7:129248996
|
C | CTT | 9 | a0001c0001t0003g0143a0001c0001t0003g0164a0001c0001t0004g0165others(6): Show | 9 | HG01952.hp1 HG01981.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+23574_363+2357 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129248996 | |||||
| chr7:129249156
|
C | T | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+23717C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249156 | ||||||
| chr7:129249184
|
G | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+23745G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249184 | ||||||
| chr7:129249396
|
A | C | 1 | a0001c0002t0003g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.363+23957A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249396 | ||||||
| chr7:129249442
|
G | A | 1 | a0001c0001t0003g0156 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.363+24003G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249442 | ||||||
| chr7:129249467
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363+24028G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249467 | ||||||
| chr7:129249474
|
G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG00408.hp1 HG00558.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+24035G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249474 | ||||||
| chr7:129249552
|
A | C | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+24113A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249552 | ||||||
| chr7:129249646
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+24207C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249646 | ||||||
| chr7:129249748
|
G | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+24309G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129249748 | ||||||
| chr7:129250048
|
C | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+24609C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250048 | ||||||
| chr7:129250176
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.363+24737G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250176 | ||||||
| chr7:129250214
|
A | G | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+24775A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250214 | ||||||
| chr7:129250318
|
G | A | 10 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(7): Show | 10 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+24879G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250318 | ||||||
| chr7:129250348
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.363+24909C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250348 | ||||||
| chr7:129250870
|
C | A | 1 | a0001c0002t0003g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.363+25431C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250870 | ||||||
| chr7:129250930
|
C | T | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+25491C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250930 | ||||||
| chr7:129250942
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+25503C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250942 | ||||||
| chr7:129250971
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.363+25532G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250971 | ||||||
| chr7:129250974
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+25535A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129250974 | ||||||
| chr7:129251207
|
A | G | 1 | a0001c0001t0003g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.363+25768A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251207 | ||||||
| chr7:129251317
|
AT | A | 14 | a0001c0001t0001g0122a0001c0001t0002g0282a0001c0001t0003g0146others(11): Show | 14 | HG00741.hp2 HG01123.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.363+25903delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129251317 | |||||
| chr7:129251317
|
ATT | A | 46 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0147others(43): Show | 46 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.363+25902_363+2590 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129251317 | |||||
| chr7:129251317
|
ATTT | A | 156 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(153): Show | 156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.363+25901_363+2590 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129251317 | |||||
| chr7:129251317
|
ATTTT | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(43): Show | 46 | HG00735.hp1 HG01074.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.363+25900_363+2590 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129251317 | |||||
| chr7:129251317
|
ATTTTT | A | 6 | a0001c0001t0002g0075a0001c0002t0001g0265a0001c0002t0002g0191others(3): Show | 6 | HG00099.hp2 HG01993.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+25899_363+2590 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129251317 | |||||
| chr7:129251546
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.363+26107C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251546 | ||||||
| chr7:129251711
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.363+26272G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251711 | ||||||
| chr7:129251818
|
C | T | 84 | a0001c0001t0003g0135a0001c0001t0003g0139a0001c0001t0003g0142others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.363+26379C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251818 | ||||||
| chr7:129251844
|
T | G | 1 | a0001c0002t0003g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.363+26405T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251844 | ||||||
| chr7:129251959
|
T | A | 3 | a0001c0001t0003g0135a0001c0001t0004g0136a0001c0001t0004g0137 | 3 | HG00140.hp1 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+26520T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129251959 | ||||||
| chr7:129252042
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.363+26603T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252042 | ||||||
| chr7:129252384
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.363+26945A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252384 | ||||||
| chr7:129252566
|
A | C | 110 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.363+27127A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252566 | ||||||
| chr7:129252580
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.363+27141A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252580 | ||||||
| chr7:129252598
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.363+27159C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252598 | ||||||
| chr7:129252695
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+27256A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252695 | ||||||
| chr7:129252758
|
C | A | 1 | a0001c0001t0005g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.363+27319C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252758 | ||||||
| chr7:129252826
|
TGATA | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+27392_363+2739 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129252826 | |||||
| chr7:129252865
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+27426G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129252865 | ||||||
| chr7:129253077
|
G | A | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+27638G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253077 | ||||||
| chr7:129253390
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+27951C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253390 | ||||||
| chr7:129253478
|
T | C | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.363+28039T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253478 | ||||||
| chr7:129253672
|
T | A | 108 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.363+28233T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253672 | ||||||
| chr7:129253743
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+28304C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253743 | ||||||
| chr7:129253906
|
T | C | 3 | a0001c0001t0003g0135a0001c0001t0004g0136a0001c0001t0004g0137 | 3 | HG00140.hp1 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+28467T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253906 | ||||||
| chr7:129253911
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+28472A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129253911 | ||||||
| chr7:129254068
|
G | A | 1 | a0001c0001t0006g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.363+28629G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254068 | ||||||
| chr7:129254342
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.363+28903C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254342 | ||||||
| chr7:129254611
|
G | T | 1 | a0001c0001t0005g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.363+29172G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254611 | ||||||
| chr7:129254680
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+29241G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254680 | ||||||
| chr7:129254683
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.363+29244G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254683 | ||||||
| chr7:129254842
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+29403G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254842 | ||||||
| chr7:129254958
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+29519A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129254958 | ||||||
| chr7:129255213
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.363+29774A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255213 | ||||||
| chr7:129255216
|
G | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.363+29777G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255216 | ||||||
| chr7:129255468
|
C | T | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+30029C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255468 | ||||||
| chr7:129255494
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 110 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.363+30055A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255494 | ||||||
| chr7:129255510
|
C | G | 1 | a0001c0001t0021g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.363+30071C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255510 | ||||||
| chr7:129255830
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.363+30391C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255830 | ||||||
| chr7:129255919
|
G | A | 2 | a0001c0002t0002g0216a0001c0002t0002g0217 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.363+30480G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129255919 | ||||||
| chr7:129255955
|
CTG | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+30520_363+3052 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129255955 | |||||
| chr7:129256051
|
G | A | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.363+30612G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256051 | ||||||
| chr7:129256267
|
A | G | 8 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0279others(5): Show | 8 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+30828A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256267 | ||||||
| chr7:129256539
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+31100C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256539 | ||||||
| chr7:129256547
|
C | CCA | 48 | a0001c0001t0001g0149a0001c0001t0001g0170a0001c0001t0001g0179others(45): Show | 48 | HG00408.hp2 HG00733.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.363+31110_363+3111 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256547 | |||||
| chr7:129256549
|
A | AC | 13 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0124others(10): Show | 13 | HG00558.hp1 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+31120dupC | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | ACAC | 56 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.363+31111_363+3111 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | ACACC | 31 | a0001c0001t0002g0004a0001c0001t0003g0146a0001c0001t0008g0150others(28): Show | 31 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+31111_363+3111 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | ACC | 31 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0032others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+31119_363+3112 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | ACCC | 55 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(52): Show | 55 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.363+31118_363+3112 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | ACCCC | 16 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0072others(13): Show | 16 | HG01167.hp2 HG01168.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+31117_363+3112 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129256549 | |||||
| chr7:129256549
|
A | C | 10 | a0001c0001t0001g0055a0001c0001t0001g0106a0001c0001t0001g0111others(7): Show | 10 | HG01168.hp2 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+31110A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256549 | ||||||
| chr7:129256570
|
A | T | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+31131A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256570 | ||||||
| chr7:129256576
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+31137T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256576 | ||||||
| chr7:129256610
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.363+31171T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129256610 | ||||||
| chr7:129257044
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+31605G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257044 | ||||||
| chr7:129257061
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+31622C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257061 | ||||||
| chr7:129257476
|
G | A | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+32037G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257476 | ||||||
| chr7:129257501
|
T | C | 154 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.363+32062T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257501 | ||||||
| chr7:129257667
|
C | T | 39 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.363+32228C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257667 | ||||||
| chr7:129257709
|
G | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+32270G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257709 | ||||||
| chr7:129257716
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+32277G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257716 | ||||||
| chr7:129257793
|
T | C | 1 | a0001c0002t0006g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+32354T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257793 | ||||||
| chr7:129257850
|
A | C | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.363+32411A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257850 | ||||||
| chr7:129257913
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+32474A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129257913 | ||||||
| chr7:129258230
|
A | AT | 28 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.363+32806dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129258230 | |||||
| chr7:129258230
|
AT | A | 8 | a0001c0001t0001g0038a0001c0001t0007g0285a0001c0001t0007g0286others(5): Show | 8 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+32806delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129258230 | |||||
| chr7:129258246
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0070 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.363+32807G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129258246 | ||||||
| chr7:129258257
|
GA | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 110 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.363+32829delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129258257 | |||||
| chr7:129258534
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+33095A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129258534 | ||||||
| chr7:129258556
|
CTT | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.363+33135_363+3313 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129258556 | |||||
| chr7:129258643
|
G | C | 1 | a0001c0001t0019g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.363+33204G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129258643 | ||||||
| chr7:129258873
|
G | T | 3 | a0001c0001t0003g0139a0001c0001t0003g0156a0001c0001t0003g0187 | 3 | NA18959.hp1 NA18982.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.363+33434G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129258873 | ||||||
| chr7:129258892
|
G | T | 1 | a0001c0001t0002g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.363+33453G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129258892 | ||||||
| chr7:129259112
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+33673C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259112 | ||||||
| chr7:129259116
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0185 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+33677C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259116 | ||||||
| chr7:129259397
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+33958C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259397 | ||||||
| chr7:129259935
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+34496G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259935 | ||||||
| chr7:129259975
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0087a0001c0001t0001g0103others(1): Show | 4 | NA18947.hp2 NA18948.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+34536C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259975 | ||||||
| chr7:129259990
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+34551C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129259990 | ||||||
| chr7:129260076
|
C | CA | 14 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0094others(11): Show | 14 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.363+34654dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129260076 | |||||
| chr7:129260598
|
C | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+35159C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260598 | ||||||
| chr7:129260628
|
G | A | 1 | a0001c0002t0003g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.363+35189G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260628 | ||||||
| chr7:129260667
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.363+35228G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260667 | ||||||
| chr7:129260858
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+35419T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260858 | ||||||
| chr7:129260912
|
C | A | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363+35473C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260912 | ||||||
| chr7:129260913
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363+35474C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129260913 | ||||||
| chr7:129261057
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.363+35618T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129261057 | ||||||
| chr7:129261111
|
T | C | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+35672T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129261111 | ||||||
| chr7:129261349
|
TAGAG | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+35913_363+3591 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129261349 | |||||
| chr7:129261372
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+35933A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129261372 | ||||||
| chr7:129261424
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+35985G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129261424 | ||||||
| chr7:129261588
|
C | A | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+36149C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129261588 | ||||||
| chr7:129262119
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.363+36680C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262119 | ||||||
| chr7:129262377
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+36938C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262377 | ||||||
| chr7:129262500
|
A | G | 2 | a0001c0002t0001g0196a0001c0002t0001g0265 | 2 | HG01993.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.363+37061A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262500 | ||||||
| chr7:129262749
|
G | A | 39 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.363+37310G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262749 | ||||||
| chr7:129262939
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | HG01081.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.363+37500G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262939 | ||||||
| chr7:129262995
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+37556A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129262995 | ||||||
| chr7:129263142
|
T | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+37703T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263142 | ||||||
| chr7:129263249
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+37810A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263249 | ||||||
| chr7:129263255
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+37816G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263255 | ||||||
| chr7:129263371
|
G | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+37932G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263371 | ||||||
| chr7:129263554
|
C | T | 1 | a0001c0002t0003g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.363+38115C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263554 | ||||||
| chr7:129263601
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0084 | 2 | HG00099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.363+38162A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263601 | ||||||
| chr7:129263874
|
T | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+38435T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129263874 | ||||||
| chr7:129264067
|
G | T | 1 | a0001c0001t0002g0034 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.363+38628G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264067 | ||||||
| chr7:129264082
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+38643C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264082 | ||||||
| chr7:129264092
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0049 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.363+38653G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264092 | ||||||
| chr7:129264123
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.363+38684A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264123 | ||||||
| chr7:129264406
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363+38967A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264406 | ||||||
| chr7:129264443
|
A | G | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+39004A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264443 | ||||||
| chr7:129264493
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.363+39054G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264493 | ||||||
| chr7:129264507
|
G | A | 1 | a0001c0001t0011g0291 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.363+39068G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264507 | ||||||
| chr7:129264682
|
G | A | 108 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.363+39243G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264682 | ||||||
| chr7:129264960
|
C | T | 82 | a0001c0001t0003g0135a0001c0001t0003g0139a0001c0001t0003g0142others(79): Show | 82 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.363+39521C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129264960 | ||||||
| chr7:129265044
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+39605A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265044 | ||||||
| chr7:129265128
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | HG01081.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.363+39689C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265128 | ||||||
| chr7:129265183
|
T | C | 2 | a0001c0002t0003g0243a0001c0002t0003g0244 | 2 | NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.363+39744T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265183 | ||||||
| chr7:129265598
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+40159T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265598 | ||||||
| chr7:129265696
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+40257T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265696 | ||||||
| chr7:129265887
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.363+40448G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129265887 | ||||||
| chr7:129266107
|
A | G | 3 | a0001c0002t0003g0193a0001c0002t0003g0221a0001c0002t0003g0266 | 3 | HG02074.hp2 NA19054.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.363+40668A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266107 | ||||||
| chr7:129266183
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+40744T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266183 | ||||||
| chr7:129266293
|
A | G | 2 | a0001c0002t0003g0237a0001c0002t0003g0239 | 2 | NA18952.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.363+40854A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266293 | ||||||
| chr7:129266524
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.363+41085C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266524 | ||||||
| chr7:129266525
|
G | A | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+41086G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266525 | ||||||
| chr7:129266704
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0174 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.363+41265G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266704 | ||||||
| chr7:129266841
|
T | C | 1 | a0001c0002t0002g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.363+41402T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266841 | ||||||
| chr7:129266931
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+41492G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129266931 | ||||||
| chr7:129267077
|
G | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 41 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.363+41638G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267077 | ||||||
| chr7:129267202
|
C | T | 1 | a0001c0001t0020g0161 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.363+41763C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267202 | ||||||
| chr7:129267217
|
A | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+41778A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267217 | ||||||
| chr7:129267230
|
G | GGT | 3 | a0001c0001t0001g0056a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG01069.hp1 HG01071.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.363+41830_363+4183 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267230 | |||||
| chr7:129267230
|
G | GGTGT | 18 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0002g0123others(15): Show | 18 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.363+41828_363+4183 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267230 | |||||
| chr7:129267230
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0001g0101a0001c0001t0001g0130 | 2 | HG00558.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.363+41822_363+4183 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267230 | |||||
| chr7:129267230
|
G | GGTGTGTG others(9): Show |
8 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175others(5): Show | 8 | HG00738.hp1 HG01243.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(20): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267230 | |||||
| chr7:129267230
|
G | GGTGTGTG others(11): Show |
6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0180others(3): Show | 6 | HG00735.hp1 HG01074.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(22): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267230 | |||||
| chr7:129267231
|
G | GTGTGTGT others(7): Show |
45 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0149others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267231 | |||||
| chr7:129267233
|
G | GTGTGTGT others(5): Show |
14 | a0001c0001t0001g0147a0001c0001t0001g0179a0001c0001t0002g0177others(11): Show | 14 | HG00408.hp2 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(16): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267233 | |||||
| chr7:129267235
|
G | GTGTGTGT others(3): Show |
82 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0030others(79): Show | 82 | HG00140.hp1 HG00597.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267235 | |||||
| chr7:129267237
|
G | GTGTGTGT others(1): Show |
89 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(12): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267237 | |||||
| chr7:129267239
|
G | GTGTGTA | 10 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0076others(7): Show | 10 | HG01123.hp1 HG03490.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(10): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267239 | |||||
| chr7:129267241
|
G | GTGTA | 5 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0002g0054others(2): Show | 5 | HG01123.hp2 HG04115.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+41805_363+4180 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129267241 | |||||
| chr7:129267358
|
G | A | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+41919G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267358 | ||||||
| chr7:129267407
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+41968C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267407 | ||||||
| chr7:129267521
|
T | C | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+42082T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267521 | ||||||
| chr7:129267917
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+42478T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129267917 | ||||||
| chr7:129268043
|
CT | C | 82 | a0001c0001t0003g0135a0001c0001t0003g0139a0001c0001t0003g0142others(79): Show | 82 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.363+42606delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129268043 | |||||
| chr7:129268047
|
C | A | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.363+42608C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268047 | ||||||
| chr7:129268092
|
A | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0079others(10): Show | 13 | HG01167.hp2 HG02735.hp1 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+42653A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268092 | ||||||
| chr7:129268114
|
A | G | 1 | a0001c0001t0008g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.363+42675A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268114 | ||||||
| chr7:129268320
|
G | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+42881G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268320 | ||||||
| chr7:129268389
|
C | G | 1 | a0001c0002t0003g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.363+42950C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268389 | ||||||
| chr7:129268432
|
C | G | 108 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.363+42993C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268432 | ||||||
| chr7:129268536
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+43097G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268536 | ||||||
| chr7:129268612
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+43173A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268612 | ||||||
| chr7:129268803
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+43364C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129268803 | ||||||
| chr7:129269030
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+43591A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269030 | ||||||
| chr7:129269112
|
T | C | 1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363+43673T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269112 | ||||||
| chr7:129269122
|
A | G | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+43683A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269122 | ||||||
| chr7:129269131
|
GTT | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.363+43706_363+4370 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129269131 | |||||
| chr7:129269137
|
T | G | 1 | a0001c0002t0002g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363+43698T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269137 | ||||||
| chr7:129269155
|
C | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+43716C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269155 | ||||||
| chr7:129269185
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+43746C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269185 | ||||||
| chr7:129269456
|
T | G | 1 | a0001c0001t0003g0154 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.363+44017T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269456 | ||||||
| chr7:129269489
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+44050A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269489 | ||||||
| chr7:129269582
|
GGTTTT | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.363+44169_363+4417 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129269582 | |||||
| chr7:129269603
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.363+44164G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269603 | ||||||
| chr7:129269748
|
T | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+44309T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269748 | ||||||
| chr7:129269886
|
T | C | 150 | a0001c0001t0001g0025a0001c0001t0001g0138a0001c0001t0001g0140others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.363+44447T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129269886 | ||||||
| chr7:129270040
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+44601C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129270040 | ||||||
| chr7:129270041
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+44602G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129270041 | ||||||
| chr7:129270113
|
G | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.363+44674G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129270113 | ||||||
| chr7:129270713
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.363+45274T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129270713 | ||||||
| chr7:129270855
|
ATT | A | 5 | a0001c0002t0003g0231a0001c0002t0003g0242a0001c0002t0003g0245others(2): Show | 5 | HG00408.hp2 HG01952.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+45418_363+4541 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129270855 | |||||
| chr7:129270900
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.363+45461T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129270900 | ||||||
| chr7:129271049
|
C | A | 2 | a0001c0001t0002g0168a0001c0001t0002g0169 | 2 | HG01069.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.363+45610C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271049 | ||||||
| chr7:129271080
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.363+45641G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271080 | ||||||
| chr7:129271133
|
C | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0020a0001c0001t0002g0043 | 3 | HG01346.hp2 HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.363+45694C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271133 | ||||||
| chr7:129271147
|
G | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+45708G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271147 | ||||||
| chr7:129271265
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.363+45826G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271265 | ||||||
| chr7:129271359
|
CA | C | 146 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0088others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.363+45940delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129271359 | |||||
| chr7:129271359
|
CAA | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+45939_363+4594 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129271359 | |||||
| chr7:129271407
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0110 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.363+45968A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271407 | ||||||
| chr7:129271481
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+46042A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271481 | ||||||
| chr7:129271524
|
A | G | 1 | a0001c0002t0002g0248 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.363+46085A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271524 | ||||||
| chr7:129271663
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.363+46224A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271663 | ||||||
| chr7:129271760
|
G | A | 1 | a0001c0005t0024g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.363+46321G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271760 | ||||||
| chr7:129271880
|
A | G | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+46441A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271880 | ||||||
| chr7:129271962
|
C | G | 3 | a0001c0002t0010g0273a0001c0002t0010g0274a0001c0002t0010g0275 | 3 | HG02683.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.363+46523C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129271962 | ||||||
| chr7:129272032
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+46593C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272032 | ||||||
| chr7:129272075
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.363+46636A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272075 | ||||||
| chr7:129272266
|
G | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+46827G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272266 | ||||||
| chr7:129272347
|
G | C | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363+46908G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272347 | ||||||
| chr7:129272360
|
T | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+46921T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272360 | ||||||
| chr7:129272408
|
G | A | 1 | a0001c0002t0002g0001 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.363+46969G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272408 | ||||||
| chr7:129272871
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+47432C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272871 | ||||||
| chr7:129272975
|
A | C | 1 | a0001c0001t0002g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.363+47536A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129272975 | ||||||
| chr7:129273205
|
C | G | 1 | a0001c0002t0003g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.363+47766C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273205 | ||||||
| chr7:129273267
|
T | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+47828T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273267 | ||||||
| chr7:129273321
|
C | CT | 87 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(84): Show | 87 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.363+47906dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129273321 | |||||
| chr7:129273321
|
C | CTT | 139 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0001g0138others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.363+47905_363+4790 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129273321 | |||||
| chr7:129273321
|
C | CTTT | 28 | a0001c0001t0001g0069a0001c0001t0002g0003a0001c0001t0002g0173others(25): Show | 28 | HG00140.hp1 HG00733.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+47904_363+4790 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129273321 | |||||
| chr7:129273406
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+47967G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273406 | ||||||
| chr7:129273529
|
T | C | 1 | a0001c0001t0004g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.363+48090T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273529 | ||||||
| chr7:129273789
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363+48350C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273789 | ||||||
| chr7:129273841
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0002g0070 | 3 | HG01891.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.363+48402T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129273841 | ||||||
| chr7:129274096
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.363+48657A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274096 | ||||||
| chr7:129274109
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0097 | 3 | NA18950.hp2 NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.363+48670T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274109 | ||||||
| chr7:129274126
|
A | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+48687A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274126 | ||||||
| chr7:129274244
|
G | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0174 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.363+48805G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274244 | ||||||
| chr7:129274464
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.363+49025C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274464 | ||||||
| chr7:129274468
|
A | C | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+49029A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274468 | ||||||
| chr7:129274485
|
C | T | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+49046C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274485 | ||||||
| chr7:129274704
|
G | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+49265G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274704 | ||||||
| chr7:129274766
|
G | A | 1 | a0001c0002t0003g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.363+49327G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274766 | ||||||
| chr7:129274977
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+49538G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129274977 | ||||||
| chr7:129275151
|
G | C | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+49712G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275151 | ||||||
| chr7:129275152
|
G | T | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+49713G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275152 | ||||||
| chr7:129275153
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0002g0049 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.363+49714C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275153 | ||||||
| chr7:129275404
|
A | G | 1 | a0001c0002t0003g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.363+49965A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275404 | ||||||
| chr7:129275612
|
G | A | 38 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(35): Show | 38 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.363+50173G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275612 | ||||||
| chr7:129275702
|
AATAG | A | 3 | a0001c0001t0002g0008a0001c0001t0018g0283a0001c0001t0018g0284 | 3 | HG01167.hp1 HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+50273_363+5027 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129275702 | |||||
| chr7:129275931
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+50492G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129275931 | ||||||
| chr7:129276008
|
A | G | 1 | a0001c0002t0003g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.363+50569A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129276008 | ||||||
| chr7:129276432
|
T | TA | 118 | a0001c0001t0001g0292a0001c0001t0002g0003a0001c0001t0002g0004others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.363+51004dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276432 | |||||
| chr7:129276432
|
T | TAA | 31 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+51003_363+5100 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276432 | |||||
| chr7:129276489
|
G | T | 10 | a0001c0002t0003g0194a0001c0002t0003g0208a0001c0002t0003g0210others(7): Show | 10 | NA18747.hp2 NA18943.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+51050G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129276489 | ||||||
| chr7:129276736
|
C | CA | 153 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.363+51312dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276736 | |||||
| chr7:129276736
|
C | CAA | 28 | a0001c0001t0001g0112a0001c0001t0001g0138a0001c0001t0001g0140others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+51311_363+5131 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276736 | |||||
| chr7:129276736
|
C | CAAA | 77 | a0001c0001t0002g0151a0001c0001t0003g0091a0001c0001t0003g0135others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.363+51310_363+5131 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276736 | |||||
| chr7:129276736
|
C | CAAAA | 10 | a0001c0001t0003g0146a0001c0001t0003g0154a0001c0001t0003g0159others(7): Show | 10 | HG02135.hp2 HG02145.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+51309_363+5131 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129276736 | |||||
| chr7:129276813
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+51374A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129276813 | ||||||
| chr7:129277154
|
GACAA | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+51721_363+5172 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129277154 | |||||
| chr7:129277278
|
C | CG | 76 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.363+51839_363+5184 others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277278 | ||||||
| chr7:129277278
|
C | CGT | 37 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(34): Show | 37 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.363+51839_363+5184 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277278 | ||||||
| chr7:129277279
|
T | G | 144 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.363+51840T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277279 | ||||||
| chr7:129277280
|
T | G | 2 | a0001c0001t0002g0008a0001c0002t0003g0193 | 2 | HG01167.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.363+51841T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277280 | ||||||
| chr7:129277392
|
C | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+51953C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277392 | ||||||
| chr7:129277526
|
T | C | 174 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.363+52087T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277526 | ||||||
| chr7:129277571
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+52132C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277571 | ||||||
| chr7:129277611
|
A | G | 1 | a0001c0001t0003g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.363+52172A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277611 | ||||||
| chr7:129277636
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+52197A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277636 | ||||||
| chr7:129277701
|
G | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+52262G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277701 | ||||||
| chr7:129277746
|
C | T | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+52307C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277746 | ||||||
| chr7:129277747
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.363+52308G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129277747 | ||||||
| chr7:129278025
|
G | A | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+52586G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129278025 | ||||||
| chr7:129278652
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+53213G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129278652 | ||||||
| chr7:129278763
|
C | CT | 70 | a0001c0001t0001g0087a0001c0001t0001g0103a0001c0001t0001g0104others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+53343dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129278763 | |||||
| chr7:129278763
|
C | CTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0002g0008others(5): Show | 8 | HG01123.hp2 HG01167.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+53342_363+5334 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129278763 | |||||
| chr7:129278810
|
T | C | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.363+53371T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129278810 | ||||||
| chr7:129278920
|
C | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+53481C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129278920 | ||||||
| chr7:129279117
|
A | T | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.363+53678A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129279117 | ||||||
| chr7:129279244
|
G | GT | 6 | a0001c0001t0001g0292a0001c0001t0002g0185a0001c0001t0011g0290others(3): Show | 6 | HG01123.hp2 HG01981.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+53819dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129279244 | |||||
| chr7:129279338
|
T | A | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.363+53899T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129279338 | ||||||
| chr7:129279719
|
T | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.363+54280T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129279719 | ||||||
| chr7:129279904
|
C | G | 1 | a0001c0002t0003g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.363+54465C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129279904 | ||||||
| chr7:129279970
|
T | A | 1 | a0001c0002t0003g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.363+54531T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129279970 | ||||||
| chr7:129280178
|
C | CT | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+54750dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280178
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0002g0031others(5): Show | 8 | HG01099.hp1 HG01496.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+54741_363+5475 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280178
|
C | CTTTTTTT others(4): Show |
113 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.363+54740_363+5475 others(15): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280178
|
C | CTTTTTTT others(5): Show |
126 | a0001c0001t0001g0074a0001c0001t0001g0138a0001c0001t0001g0147others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.363+54750_363+5475 others(16): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280178
|
C | CTTTTTTT others(6): Show |
18 | a0001c0001t0001g0019a0001c0001t0001g0181a0001c0001t0002g0009others(15): Show | 18 | HG01074.hp2 HG01981.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.363+54750_363+5475 others(17): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280178
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0003g0154a0001c0001t0004g0144a0001c0002t0003g0247 | 3 | HG03831.hp1 NA18972.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.363+54750_363+5475 others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280178 | |||||
| chr7:129280201
|
G | A | 9 | a0001c0002t0001g0203a0001c0002t0002g0192a0001c0002t0002g0204others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+54762G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280201 | ||||||
| chr7:129280272
|
C | G | 2 | a0001c0001t0003g0139a0001c0001t0003g0156 | 2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.363+54833C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280272 | ||||||
| chr7:129280357
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.363+54918C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280357 | ||||||
| chr7:129280379
|
G | C | 1 | a0001c0002t0002g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.363+54940G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280379 | ||||||
| chr7:129280424
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+54985C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280424 | ||||||
| chr7:129280867
|
C | CT | 8 | a0001c0001t0001g0055a0001c0001t0004g0141a0001c0001t0007g0285others(5): Show | 8 | HG01099.hp1 HG01361.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+55443dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280867 | |||||
| chr7:129280916
|
G | A | 1 | a0001c0001t0002g0006 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.363+55477G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129280916 | ||||||
| chr7:129280957
|
T | TG | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+55520dupG | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129280957 | |||||
| chr7:129281221
|
A | T | 1 | a0001c0002t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.363+55782A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281221 | ||||||
| chr7:129281303
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.363+55864T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281303 | ||||||
| chr7:129281465
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.363+56026T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281465 | ||||||
| chr7:129281489
|
A | AT | 45 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0024others(42): Show | 45 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.363+56075dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129281489 | |||||
| chr7:129281489
|
AT | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0055others(6): Show | 9 | HG00423.hp1 HG01123.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+56075delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129281489 | |||||
| chr7:129281565
|
C | T | 1 | a0001c0002t0003g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.363+56126C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281565 | ||||||
| chr7:129281707
|
G | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+56268G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281707 | ||||||
| chr7:129281872
|
G | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0156 | 2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.363+56433G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129281872 | ||||||
| chr7:129282017
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.363+56578C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282017 | ||||||
| chr7:129282181
|
G | A | 1 | a0001c0002t0003g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.363+56742G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282181 | ||||||
| chr7:129282272
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+56833A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282272 | ||||||
| chr7:129282322
|
A | T | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+56883A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282322 | ||||||
| chr7:129282366
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0003g0162 | 2 | HG02135.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.363+56927C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282366 | ||||||
| chr7:129282591
|
C | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.363+57152C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282591 | ||||||
| chr7:129282820
|
T | C | 2 | a0001c0001t0013g0118a0001c0001t0013g0119 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.363+57381T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282820 | ||||||
| chr7:129282928
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+57489G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129282928 | ||||||
| chr7:129283082
|
C | A | 1 | a0001c0001t0003g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.363+57643C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129283082 | ||||||
| chr7:129283150
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+57711T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129283150 | ||||||
| chr7:129283961
|
T | A | 40 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.363+58522T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129283961 | ||||||
| chr7:129283976
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+58537C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129283976 | ||||||
| chr7:129284025
|
T | C | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+58586T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284025 | ||||||
| chr7:129284066
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.363+58627T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284066 | ||||||
| chr7:129284104
|
T | C | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+58665T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284104 | ||||||
| chr7:129284282
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363+58843C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284282 | ||||||
| chr7:129284325
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+58886T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284325 | ||||||
| chr7:129284435
|
A | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+58996A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284435 | ||||||
| chr7:129284599
|
C | CA | 34 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0038others(31): Show | 34 | HG00597.hp1 HG00735.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.363+59180dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129284599 | |||||
| chr7:129284640
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+59201G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129284640 | ||||||
| chr7:129285069
|
G | A | 83 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.363+59630G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285069 | ||||||
| chr7:129285090
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.363+59651G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285090 | ||||||
| chr7:129285201
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.363+59762T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285201 | ||||||
| chr7:129285376
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.363+59937T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285376 | ||||||
| chr7:129285623
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.363+60184C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285623 | ||||||
| chr7:129285696
|
CT | C | 47 | a0001c0001t0001g0044a0001c0001t0001g0103a0001c0001t0002g0003others(44): Show | 47 | HG00099.hp1 HG00673.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.363+60278delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129285696 | |||||
| chr7:129285696
|
CTT | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.363+60277_363+6027 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129285696 | |||||
| chr7:129285696
|
CTTT | C | 93 | a0001c0001t0001g0105a0001c0001t0001g0171a0001c0001t0001g0172others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.363+60276_363+6027 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129285696 | |||||
| chr7:129285824
|
C | A | 4 | a0001c0002t0003g0208a0001c0002t0003g0222a0001c0002t0003g0223others(1): Show | 4 | NA18747.hp2 NA18943.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+60385C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129285824 | ||||||
| chr7:129286036
|
C | T | 1 | a0001c0002t0003g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.363+60597C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286036 | ||||||
| chr7:129286045
|
A | G | 1 | a0001c0001t0022g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.363+60606A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286045 | ||||||
| chr7:129286119
|
G | A | 2 | a0001c0002t0001g0267a0001c0002t0001g0269 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.363+60680G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286119 | ||||||
| chr7:129286231
|
G | A | 2 | a0001c0002t0002g0204a0001c0002t0002g0249 | 2 | HG01433.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.363+60792G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286231 | ||||||
| chr7:129286291
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+60852C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286291 | ||||||
| chr7:129286451
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+61012G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286451 | ||||||
| chr7:129286522
|
A | G | 1 | a0001c0001t0003g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.363+61083A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286522 | ||||||
| chr7:129286826
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+61387A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129286826 | ||||||
| chr7:129287075
|
C | CA | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.363+61637dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129287075 | |||||
| chr7:129287179
|
C | A | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+61740C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287179 | ||||||
| chr7:129287181
|
G | T | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+61742G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287181 | ||||||
| chr7:129287565
|
G | A | 111 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.363+62126G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287565 | ||||||
| chr7:129287692
|
G | C | 1 | a0001c0002t0003g0231 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.363+62253G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287692 | ||||||
| chr7:129287783
|
C | T | 2 | a0001c0002t0002g0204a0001c0002t0002g0249 | 2 | HG01433.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.363+62344C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287783 | ||||||
| chr7:129287818
|
T | C | 111 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.363+62379T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287818 | ||||||
| chr7:129287944
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+62505T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129287944 | ||||||
| chr7:129288363
|
A | T | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0002t0002g0001 | 3 | HG02735.hp1 HG03669.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.363+62924A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288363 | ||||||
| chr7:129288364
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+62925A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288364 | ||||||
| chr7:129288368
|
T | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0001t0018g0283others(3): Show | 6 | HG01891.hp1 HG03098.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+62929T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288368 | ||||||
| chr7:129288429
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+62990C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288429 | ||||||
| chr7:129288470
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01168.hp1 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.363+63031C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288470 | ||||||
| chr7:129288596
|
G | A | 43 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.363+63157G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288596 | ||||||
| chr7:129288668
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0110 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.363+63229A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129288668 | ||||||
| chr7:129289122
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+63683C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289122 | ||||||
| chr7:129289309
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+63870C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289309 | ||||||
| chr7:129289352
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+63913C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289352 | ||||||
| chr7:129289372
|
G | A | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+63933G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289372 | ||||||
| chr7:129289456
|
G | A | 1 | a0001c0002t0002g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.363+64017G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289456 | ||||||
| chr7:129289467
|
T | G | 6 | a0001c0001t0012g0114a0001c0001t0012g0131a0001c0001t0013g0118others(3): Show | 6 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+64028T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289467 | ||||||
| chr7:129289513
|
C | A | 2 | a0001c0002t0003g0195a0001c0002t0003g0235 | 2 | NA18979.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.363+64074C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289513 | ||||||
| chr7:129289638
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+64199G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289638 | ||||||
| chr7:129289639
|
G | T | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+64200G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289639 | ||||||
| chr7:129289680
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+64241G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289680 | ||||||
| chr7:129289789
|
C | CT | 39 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.363+64361dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129289789 | |||||
| chr7:129289885
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+64446T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129289885 | ||||||
| chr7:129290002
|
G | A | 1 | a0001c0002t0003g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.363+64563G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290002 | ||||||
| chr7:129290028
|
C | T | 1 | a0001c0002t0003g0227 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.363+64589C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290028 | ||||||
| chr7:129290278
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.363+64839C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290278 | ||||||
| chr7:129290285
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+64846C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290285 | ||||||
| chr7:129290424
|
C | G | 151 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.363+64985C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290424 | ||||||
| chr7:129290466
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+65027A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290466 | ||||||
| chr7:129290656
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.363+65217C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290656 | ||||||
| chr7:129290726
|
C | T | 1 | a0001c0001t0021g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.363+65287C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290726 | ||||||
| chr7:129290812
|
C | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+65373C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290812 | ||||||
| chr7:129290855
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+65416G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290855 | ||||||
| chr7:129290876
|
G | C | 2 | a0001c0001t0001g0115a0001c0002t0001g0250 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.363+65437G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290876 | ||||||
| chr7:129290987
|
C | T | 109 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.363+65548C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129290987 | ||||||
| chr7:129291014
|
A | G | 2 | a0001c0001t0003g0145a0001c0001t0004g0144 | 2 | HG03831.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.363+65575A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291014 | ||||||
| chr7:129291019
|
A | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+65580A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291019 | ||||||
| chr7:129291069
|
C | T | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+65630C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291069 | ||||||
| chr7:129291113
|
C | T | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+65674C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291113 | ||||||
| chr7:129291514
|
C | CT | 33 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(30): Show | 33 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.363+66091dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129291514 | |||||
| chr7:129291575
|
A | G | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+66136A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291575 | ||||||
| chr7:129291611
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+66172C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291611 | ||||||
| chr7:129291612
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+66173T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291612 | ||||||
| chr7:129291628
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.363+66189G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291628 | ||||||
| chr7:129291637
|
G | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.363+66198G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291637 | ||||||
| chr7:129291649
|
C | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+66210C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291649 | ||||||
| chr7:129291712
|
T | TC | 269 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.363+66274dupC | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129291712 | |||||
| chr7:129291824
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+66385C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291824 | ||||||
| chr7:129291852
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+66413G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129291852 | ||||||
| chr7:129292129
|
G | A | 1 | a0001c0002t0002g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.363+66690G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292129 | ||||||
| chr7:129292199
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+66760G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292199 | ||||||
| chr7:129292239
|
T | C | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+66800T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292239 | ||||||
| chr7:129292369
|
A | G | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.363+66930A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292369 | ||||||
| chr7:129292402
|
G | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+66963G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292402 | ||||||
| chr7:129292655
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.363+67216T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292655 | ||||||
| chr7:129292844
|
A | C | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.363+67405A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292844 | ||||||
| chr7:129292908
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+67469A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292908 | ||||||
| chr7:129292967
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG03225.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.363+67528A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129292967 | ||||||
| chr7:129293005
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+67566G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293005 | ||||||
| chr7:129293146
|
TG | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 138 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.363+67710delG | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129293146 | |||||
| chr7:129293149
|
G | T | 2 | a0001c0001t0002g0282a0001c0001t0021g0092 | 2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.363+67710G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293149 | ||||||
| chr7:129293149
|
GT | G | 110 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.363+67720delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129293149 | |||||
| chr7:129293206
|
C | T | 1 | a0001c0002t0003g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.363+67767C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293206 | ||||||
| chr7:129293433
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.363+67994C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293433 | ||||||
| chr7:129293602
|
G | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+68163G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293602 | ||||||
| chr7:129293640
|
T | TA | 6 | a0001c0001t0002g0023a0001c0001t0008g0184a0001c0002t0002g0216others(3): Show | 6 | HG01361.hp2 HG02647.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+68211dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129293640 | |||||
| chr7:129293651
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+68212C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293651 | ||||||
| chr7:129293666
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0029others(7): Show | 10 | HG01346.hp2 HG01433.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+68227T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293666 | ||||||
| chr7:129293686
|
A | G | 2 | a0001c0002t0002g0212a0001c0002t0002g0251 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.363+68247A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293686 | ||||||
| chr7:129293716
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.363+68277A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293716 | ||||||
| chr7:129293807
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0185 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+68368T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293807 | ||||||
| chr7:129293963
|
T | C | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.363+68524T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293963 | ||||||
| chr7:129293995
|
T | G | 1 | a0001c0001t0002g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.363+68556T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129293995 | ||||||
| chr7:129294017
|
TTTAGA | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.363+68582_363+6858 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129294017 | |||||
| chr7:129294092
|
T | G | 1 | a0002c0003t0002g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363+68653T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294092 | ||||||
| chr7:129294185
|
T | C | 1 | a0001c0002t0017g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363+68746T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294185 | ||||||
| chr7:129294202
|
G | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.363+68763G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294202 | ||||||
| chr7:129294333
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+68894G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294333 | ||||||
| chr7:129294337
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+68898C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294337 | ||||||
| chr7:129294448
|
TA | T | 91 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.363+69010delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294448 | ||||||
| chr7:129294561
|
A | T | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+69122A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294561 | ||||||
| chr7:129294732
|
C | T | 10 | a0001c0002t0001g0203a0001c0002t0002g0192a0001c0002t0002g0204others(7): Show | 10 | HG01433.hp2 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+69293C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294732 | ||||||
| chr7:129294733
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+69294G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129294733 | ||||||
| chr7:129295168
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+69729G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129295168 | ||||||
| chr7:129295174
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.363+69735T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129295174 | ||||||
| chr7:129295552
|
C | T | 4 | a0001c0002t0001g0263a0001c0002t0003g0197a0001c0002t0003g0209others(1): Show | 4 | HG00741.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+70113C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129295552 | ||||||
| chr7:129295611
|
G | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG03225.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.363+70172G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129295611 | ||||||
| chr7:129296098
|
T | C | 1 | a0001c0001t0003g0182 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.363+70659T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129296098 | ||||||
| chr7:129296268
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+70829A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129296268 | ||||||
| chr7:129296438
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+70999G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129296438 | ||||||
| chr7:129296871
|
A | T | 1 | a0001c0001t0017g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+71432A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129296871 | ||||||
| chr7:129297294
|
A | T | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.363+71855A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129297294 | ||||||
| chr7:129297529
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+72090T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129297529 | ||||||
| chr7:129297749
|
C | T | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.363+72310C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129297749 | ||||||
| chr7:129298068
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0002g0054 | 3 | NA18942.hp1 NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.363+72629T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298068 | ||||||
| chr7:129298185
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+72746G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298185 | ||||||
| chr7:129298211
|
A | C | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.363+72772A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298211 | ||||||
| chr7:129298291
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+72852C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298291 | ||||||
| chr7:129298398
|
G | A | 83 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.363+72959G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298398 | ||||||
| chr7:129298401
|
A | G | 1 | a0001c0002t0003g0209 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.363+72962A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298401 | ||||||
| chr7:129298570
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+73131C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298570 | ||||||
| chr7:129298936
|
T | G | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.363+73497T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129298936 | ||||||
| chr7:129299106
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.363+73667A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299106 | ||||||
| chr7:129299124
|
G | T | 1 | a0001c0001t0017g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+73685G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299124 | ||||||
| chr7:129299222
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363+73783C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299222 | ||||||
| chr7:129299234
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.363+73795G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299234 | ||||||
| chr7:129299280
|
C | CA | 106 | a0001c0001t0001g0035a0001c0001t0001g0138a0001c0001t0001g0140others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.363+73854dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299280 | |||||
| chr7:129299280
|
C | CAA | 13 | a0001c0001t0002g0176a0001c0001t0003g0139a0001c0001t0003g0156others(10): Show | 13 | HG01099.hp1 HG01109.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+73853_363+7385 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299280 | |||||
| chr7:129299294
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+73855C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299294 | ||||||
| chr7:129299309
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.363+73870G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299309 | ||||||
| chr7:129299361
|
T | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+73922T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299361 | ||||||
| chr7:129299369
|
G | GT | 7 | a0001c0001t0001g0292a0001c0001t0003g0145a0001c0002t0003g0195others(4): Show | 7 | HG02109.hp1 HG03491.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+73972dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTT | 12 | a0001c0001t0004g0007a0001c0002t0001g0265a0001c0002t0003g0194others(9): Show | 12 | HG00597.hp1 HG01993.hp1 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.363+73971_363+7397 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTT | 6 | a0001c0002t0002g0200a0001c0002t0002g0262a0001c0002t0002g0277others(3): Show | 6 | HG00408.hp2 HG02818.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+73969_363+7397 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT | 6 | a0001c0002t0001g0270a0001c0002t0002g0212a0001c0002t0003g0206others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+73966_363+7397 others(11): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(3): Show |
1 | a0001c0002t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.363+73963_363+7397 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0003g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.363+73961_363+7397 others(16): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(6): Show |
2 | a0001c0002t0002g0251a0001c0002t0003g0272 | 2 | HG01243.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.363+73960_363+7397 others(17): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0002g0006 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.363+73958_363+7397 others(19): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0002g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.363+73956_363+7397 others(21): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
G | GTTTTTTT others(12): Show |
1 | a0001c0002t0002g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.363+73954_363+7397 others(23): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GT | G | 15 | a0001c0001t0003g0091a0001c0001t0003g0157a0001c0001t0003g0162others(12): Show | 15 | HG00558.hp1 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.363+73972delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTT | G | 9 | a0001c0001t0002g0167a0001c0001t0003g0164a0001c0001t0003g0187others(6): Show | 9 | HG00741.hp2 HG01109.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+73971_363+7397 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTT | G | 18 | a0001c0001t0002g0176a0001c0001t0003g0139a0001c0001t0003g0143others(15): Show | 18 | HG01346.hp1 HG01361.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.363+73970_363+7397 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTT | G | 9 | a0001c0001t0003g0160a0001c0001t0004g0166a0001c0001t0020g0161others(6): Show | 9 | HG00738.hp2 HG01081.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+73969_363+7397 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT | G | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0171others(9): Show | 12 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+73966_363+7397 others(11): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(1): Show |
G | 7 | a0001c0001t0001g0138a0001c0001t0001g0174a0001c0001t0001g0180others(4): Show | 7 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+73965_363+7397 others(12): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0002g0003 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.363+73963_363+7397 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0007g0288a0001c0002t0017g0253 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.363+73959_363+7397 others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(8): Show |
G | 10 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0103others(7): Show | 10 | HG00733.hp2 HG01099.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+73958_363+7397 others(19): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(9): Show |
G | 34 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(31): Show | 34 | HG00423.hp1 HG00597.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.363+73957_363+7397 others(20): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(10): Show |
G | 71 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(68): Show | 71 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.363+73956_363+7397 others(21): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(12): Show |
G | 5 | a0001c0001t0001g0115a0001c0001t0002g0129a0001c0001t0006g0117others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+73954_363+7397 others(23): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(13): Show |
G | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0130others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.363+73953_363+7397 others(24): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(16): Show |
G | 4 | a0001c0001t0011g0290a0001c0001t0011g0291a0001c0002t0002g0204others(1): Show | 4 | HG01123.hp2 HG01433.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+73950_363+7397 others(27): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299369
|
GTTTTTTT others(17): Show |
G | 4 | a0001c0001t0003g0182a0001c0001t0018g0283a0001c0001t0018g0284others(1): Show | 4 | HG01891.hp1 NA18969.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+73949_363+7397 others(28): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129299369 | |||||
| chr7:129299554
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.363+74115G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299554 | ||||||
| chr7:129299604
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.363+74165A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299604 | ||||||
| chr7:129299645
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+74206G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299645 | ||||||
| chr7:129299663
|
G | T | 1 | a0001c0002t0001g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.363+74224G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299663 | ||||||
| chr7:129299681
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+74242T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299681 | ||||||
| chr7:129299719
|
G | A | 1 | a0001c0002t0017g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363+74280G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299719 | ||||||
| chr7:129299741
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.363+74302G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299741 | ||||||
| chr7:129299871
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+74432C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129299871 | ||||||
| chr7:129300219
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+74780C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300219 | ||||||
| chr7:129300278
|
C | A | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+74839C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300278 | ||||||
| chr7:129300335
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.363+74896A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300335 | ||||||
| chr7:129300376
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+74937A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300376 | ||||||
| chr7:129300442
|
A | G | 1 | a0001c0001t0006g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.363+75003A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300442 | ||||||
| chr7:129300508
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+75069G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300508 | ||||||
| chr7:129300553
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.363+75114A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300553 | ||||||
| chr7:129300619
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.363+75180A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300619 | ||||||
| chr7:129300659
|
T | C | 29 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+75220T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300659 | ||||||
| chr7:129300768
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+75329C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300768 | ||||||
| chr7:129300802
|
G | A | 1 | a0001c0001t0006g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.363+75363G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300802 | ||||||
| chr7:129300873
|
C | T | 1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363+75434C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129300873 | ||||||
| chr7:129301009
|
T | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.363+75570T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129301009 | ||||||
| chr7:129301284
|
G | A | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.363+75845G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129301284 | ||||||
| chr7:129301610
|
A | T | 1 | a0001c0001t0003g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.363+76171A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129301610 | ||||||
| chr7:129301874
|
A | AT | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.363+76445dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129301874 | |||||
| chr7:129302143
|
T | C | 2 | a0001c0002t0003g0240a0001c0002t0003g0241 | 2 | NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.363+76704T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302143 | ||||||
| chr7:129302150
|
C | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.363+76711C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302150 | ||||||
| chr7:129302288
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.363+76849T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302288 | ||||||
| chr7:129302320
|
T | G | 1 | a0002c0003t0002g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363+76881T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302320 | ||||||
| chr7:129302348
|
C | CT | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.363+76911dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129302348 | |||||
| chr7:129302391
|
G | A | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+76952G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302391 | ||||||
| chr7:129302653
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-76985G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302653 | ||||||
| chr7:129302721
|
T | C | 2 | a0001c0001t0002g0031a0003c0004t0001g0042 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.364-76917T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302721 | ||||||
| chr7:129302870
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.364-76768A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302870 | ||||||
| chr7:129302950
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-76688T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129302950 | ||||||
| chr7:129303061
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.364-76577C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303061 | ||||||
| chr7:129303092
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-76546C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303092 | ||||||
| chr7:129303093
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.364-76545G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303093 | ||||||
| chr7:129303135
|
C | T | 1 | a0001c0002t0003g0223 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.364-76503C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303135 | ||||||
| chr7:129303161
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.364-76477C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303161 | ||||||
| chr7:129303210
|
G | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-76428G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303210 | ||||||
| chr7:129303257
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.364-76381C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303257 | ||||||
| chr7:129303774
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-75864G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129303774 | ||||||
| chr7:129304009
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-75629C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304009 | ||||||
| chr7:129304017
|
C | G | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-75621C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304017 | ||||||
| chr7:129304084
|
TAAAC | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-75545_364-7554 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129304084 | |||||
| chr7:129304450
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-75188G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304450 | ||||||
| chr7:129304594
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-75044C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304594 | ||||||
| chr7:129304670
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-74968A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304670 | ||||||
| chr7:129304844
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-74794T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304844 | ||||||
| chr7:129304876
|
A | G | 1 | a0001c0002t0004g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.364-74762A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304876 | ||||||
| chr7:129304883
|
A | G | 2 | a0001c0002t0002g0254a0001c0002t0017g0253 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.364-74755A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304883 | ||||||
| chr7:129304935
|
G | GT | 23 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.364-74693dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129304935 | |||||
| chr7:129304965
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-74673T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129304965 | ||||||
| chr7:129305043
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.364-74595A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305043 | ||||||
| chr7:129305097
|
C | T | 2 | a0001c0002t0002g0200a0002c0003t0002g0199 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.364-74541C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305097 | ||||||
| chr7:129305131
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0002g0054 | 3 | NA18942.hp1 NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.364-74507C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305131 | ||||||
| chr7:129305184
|
G | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-74454G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305184 | ||||||
| chr7:129305232
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-74406C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305232 | ||||||
| chr7:129305243
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-74395C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305243 | ||||||
| chr7:129305330
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-74308C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305330 | ||||||
| chr7:129305384
|
C | T | 1 | a0001c0002t0003g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.364-74254C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305384 | ||||||
| chr7:129305385
|
G | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-74253G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305385 | ||||||
| chr7:129305477
|
C | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0279others(4): Show | 7 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-74161C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305477 | ||||||
| chr7:129305495
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364-74143A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305495 | ||||||
| chr7:129305743
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.364-73895T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305743 | ||||||
| chr7:129305839
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-73799T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129305839 | ||||||
| chr7:129306130
|
C | A | 2 | a0001c0002t0003g0195a0001c0002t0003g0235 | 2 | NA18979.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.364-73508C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306130 | ||||||
| chr7:129306479
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364-73159G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306479 | ||||||
| chr7:129306564
|
ATC | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-73070_364-7306 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129306564 | |||||
| chr7:129306572
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-73066T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306572 | ||||||
| chr7:129306722
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364-72916C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306722 | ||||||
| chr7:129306853
|
G | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-72785G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306853 | ||||||
| chr7:129306889
|
A | C | 3 | a0001c0002t0010g0273a0001c0002t0010g0274a0001c0002t0010g0275 | 3 | HG02683.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.364-72749A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306889 | ||||||
| chr7:129306890
|
G | C | 3 | a0001c0002t0010g0273a0001c0002t0010g0274a0001c0002t0010g0275 | 3 | HG02683.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.364-72748G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129306890 | ||||||
| chr7:129307035
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG01257.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.364-72603G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307035 | ||||||
| chr7:129307069
|
A | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-72569A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307069 | ||||||
| chr7:129307129
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-72509T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307129 | ||||||
| chr7:129307380
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-72258C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307380 | ||||||
| chr7:129307699
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.364-71939C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307699 | ||||||
| chr7:129307879
|
C | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-71759C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129307879 | ||||||
| chr7:129308071
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-71567G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129308071 | ||||||
| chr7:129308150
|
C | T | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-71488C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129308150 | ||||||
| chr7:129308179
|
TCCTAGTG others(10): Show |
T | 4 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0005g0051others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-71455_364-7143 others(21): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129308179 | |||||
| chr7:129308340
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.364-71298C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129308340 | ||||||
| chr7:129308437
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-71201A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129308437 | ||||||
| chr7:129309092
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-70546C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309092 | ||||||
| chr7:129309158
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.364-70480G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309158 | ||||||
| chr7:129309395
|
T | C | 10 | a0001c0002t0003g0194a0001c0002t0003g0208a0001c0002t0003g0210others(7): Show | 10 | NA18747.hp2 NA18943.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-70243T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309395 | ||||||
| chr7:129309431
|
G | A | 1 | a0001c0002t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.364-70207G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309431 | ||||||
| chr7:129309467
|
G | C | 3 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287 | 3 | HG01099.hp1 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.364-70171G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309467 | ||||||
| chr7:129309677
|
T | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-69961T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309677 | ||||||
| chr7:129309817
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-69821G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309817 | ||||||
| chr7:129309907
|
A | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-69731A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129309907 | ||||||
| chr7:129310230
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-69408A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129310230 | ||||||
| chr7:129310292
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.364-69346G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129310292 | ||||||
| chr7:129310433
|
G | T | 1 | a0001c0002t0002g0249 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.364-69205G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129310433 | ||||||
| chr7:129310506
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-69132A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129310506 | ||||||
| chr7:129310836
|
G | A | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-68802G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129310836 | ||||||
| chr7:129311105
|
C | CA | 21 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0097others(18): Show | 21 | HG00423.hp2 HG01099.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-68518dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129311105 | |||||
| chr7:129311159
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-68479G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311159 | ||||||
| chr7:129311391
|
G | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-68247G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311391 | ||||||
| chr7:129311413
|
C | G | 1 | a0001c0001t0003g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.364-68225C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311413 | ||||||
| chr7:129311561
|
G | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-68077G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311561 | ||||||
| chr7:129311628
|
C | G | 2 | a0001c0002t0003g0208a0001c0002t0003g0222 | 2 | NA18747.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.364-68010C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311628 | ||||||
| chr7:129311658
|
T | G | 1 | a0001c0001t0003g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364-67980T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311658 | ||||||
| chr7:129311821
|
C | T | 1 | a0001c0001t0022g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.364-67817C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129311821 | ||||||
| chr7:129312029
|
C | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-67609C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312029 | ||||||
| chr7:129312083
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG03225.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.364-67555G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312083 | ||||||
| chr7:129312122
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-67516G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312122 | ||||||
| chr7:129312203
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-67435A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312203 | ||||||
| chr7:129312333
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-67305G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312333 | ||||||
| chr7:129312611
|
T | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-67027T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312611 | ||||||
| chr7:129312657
|
C | T | 3 | a0001c0002t0003g0237a0001c0002t0003g0238a0001c0002t0003g0239 | 3 | NA18952.hp1 NA18955.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.364-66981C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312657 | ||||||
| chr7:129312719
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-66919G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312719 | ||||||
| chr7:129312832
|
G | A | 110 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.364-66806G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129312832 | ||||||
| chr7:129313024
|
A | G | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-66614A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313024 | ||||||
| chr7:129313254
|
T | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-66384T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313254 | ||||||
| chr7:129313268
|
A | G | 1 | a0002c0003t0002g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.364-66370A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313268 | ||||||
| chr7:129313388
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.364-66250T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313388 | ||||||
| chr7:129313507
|
A | G | 10 | a0001c0001t0003g0091a0001c0002t0002g0001a0001c0002t0002g0215others(7): Show | 10 | HG00558.hp1 HG02165.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-66131A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313507 | ||||||
| chr7:129313529
|
G | T | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-66109G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313529 | ||||||
| chr7:129313579
|
T | G | 1 | a0001c0002t0003g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364-66059T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313579 | ||||||
| chr7:129313651
|
T | A | 1 | a0001c0002t0003g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.364-65987T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313651 | ||||||
| chr7:129313861
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.364-65777A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313861 | ||||||
| chr7:129313952
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-65686T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313952 | ||||||
| chr7:129313993
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0053 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364-65645A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129313993 | ||||||
| chr7:129314015
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.364-65623A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314015 | ||||||
| chr7:129314019
|
A | G | 1 | a0001c0002t0003g0241 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.364-65619A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314019 | ||||||
| chr7:129314038
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-65600T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314038 | ||||||
| chr7:129314566
|
A | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-65072A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314566 | ||||||
| chr7:129314754
|
C | T | 251 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.364-64884C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314754 | ||||||
| chr7:129314852
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-64786T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129314852 | ||||||
| chr7:129315018
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-64620T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315018 | ||||||
| chr7:129315111
|
A | C | 1 | a0001c0001t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.364-64527A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315111 | ||||||
| chr7:129315149
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-64489T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315149 | ||||||
| chr7:129315192
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-64446A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315192 | ||||||
| chr7:129315229
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-64409T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315229 | ||||||
| chr7:129315552
|
T | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0186 | 3 | HG00140.hp2 HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.364-64086T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315552 | ||||||
| chr7:129315564
|
C | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0279others(5): Show | 8 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-64074C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315564 | ||||||
| chr7:129315757
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-63881C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315757 | ||||||
| chr7:129315796
|
G | GA | 4 | a0001c0001t0011g0290a0001c0001t0011g0291a0001c0001t0018g0283others(1): Show | 4 | HG01123.hp2 HG01891.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-63836dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129315796 | |||||
| chr7:129315928
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-63710C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129315928 | ||||||
| chr7:129316058
|
T | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0053 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364-63580T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316058 | ||||||
| chr7:129316415
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-63223C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316415 | ||||||
| chr7:129316467
|
G | A | 1 | a0001c0002t0003g0224 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.364-63171G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316467 | ||||||
| chr7:129316569
|
G | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-63069G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316569 | ||||||
| chr7:129316649
|
T | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-62989T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316649 | ||||||
| chr7:129316791
|
A | G | 1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.364-62847A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316791 | ||||||
| chr7:129316894
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.364-62744T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129316894 | ||||||
| chr7:129317145
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-62493A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317145 | ||||||
| chr7:129317355
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.364-62283C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317355 | ||||||
| chr7:129317361
|
G | A | 1 | a0001c0002t0003g0223 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.364-62277G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317361 | ||||||
| chr7:129317506
|
T | C | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-62132T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317506 | ||||||
| chr7:129317525
|
G | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-62113G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317525 | ||||||
| chr7:129317538
|
C | G | 30 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(27): Show | 30 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.364-62100C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317538 | ||||||
| chr7:129317882
|
G | A | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.364-61756G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129317882 | ||||||
| chr7:129318095
|
C | T | 1 | a0001c0002t0006g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.364-61543C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129318095 | ||||||
| chr7:129318113
|
G | A | 21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.364-61525G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129318113 | ||||||
| chr7:129318167
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-61471T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129318167 | ||||||
| chr7:129318585
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-61053G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129318585 | ||||||
| chr7:129318787
|
AT | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-60839delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129318787 | |||||
| chr7:129318931
|
T | A | 4 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0005g0051others(1): Show | 4 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-60707T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129318931 | ||||||
| chr7:129319219
|
G | T | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-60419G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319219 | ||||||
| chr7:129319450
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-60188A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319450 | ||||||
| chr7:129319478
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-60160C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319478 | ||||||
| chr7:129319512
|
A | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-60126A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319512 | ||||||
| chr7:129319586
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-60052A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319586 | ||||||
| chr7:129319737
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-59901C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319737 | ||||||
| chr7:129319765
|
G | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.364-59873G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319765 | ||||||
| chr7:129319791
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-59847A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319791 | ||||||
| chr7:129319805
|
T | A | 1 | a0001c0001t0002g0021 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.364-59833T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129319805 | ||||||
| chr7:129319906
|
A | AT | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(19): Show | 22 | HG00423.hp1 HG00597.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-59721dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129319906 | |||||
| chr7:129320108
|
A | G | 1 | a0001c0001t0004g0158 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.364-59530A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320108 | ||||||
| chr7:129320300
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.364-59338G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320300 | ||||||
| chr7:129320433
|
C | T | 1 | a0001c0002t0003g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364-59205C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320433 | ||||||
| chr7:129320563
|
G | A | 83 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.364-59075G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320563 | ||||||
| chr7:129320626
|
A | T | 4 | a0001c0002t0002g0200a0001c0002t0002g0212a0001c0002t0002g0251others(1): Show | 4 | HG01243.hp1 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-59012A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320626 | ||||||
| chr7:129320665
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | HG01081.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.364-58973C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320665 | ||||||
| chr7:129320832
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.364-58806C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320832 | ||||||
| chr7:129320847
|
G | A | 2 | a0001c0002t0003g0213a0001c0002t0003g0214 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.364-58791G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129320847 | ||||||
| chr7:129321003
|
T | G | 1 | a0001c0002t0002g0001 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.364-58635T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321003 | ||||||
| chr7:129321030
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-58608C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321030 | ||||||
| chr7:129321142
|
T | C | 1 | a0001c0001t0008g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.364-58496T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321142 | ||||||
| chr7:129321272
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-58366A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321272 | ||||||
| chr7:129321302
|
T | A | 20 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(17): Show | 20 | HG00408.hp1 HG00558.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.364-58336T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321302 | ||||||
| chr7:129321358
|
A | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-58280A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321358 | ||||||
| chr7:129321652
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-57986T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321652 | ||||||
| chr7:129321743
|
G | GT | 59 | a0001c0001t0002g0167a0001c0001t0002g0173a0001c0001t0002g0175others(56): Show | 59 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.364-57874dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129321743 | |||||
| chr7:129321743
|
GT | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.364-57874delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129321743 | |||||
| chr7:129321743
|
GTTT | G | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-57876_364-5787 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129321743 | |||||
| chr7:129321754
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.364-57884T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321754 | ||||||
| chr7:129321766
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.364-57872G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321766 | ||||||
| chr7:129321772
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.364-57866G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321772 | ||||||
| chr7:129321778
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.364-57860T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321778 | ||||||
| chr7:129321789
|
T | G | 5 | a0001c0001t0004g0166a0001c0002t0001g0267a0001c0002t0001g0269others(2): Show | 5 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-57849T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321789 | ||||||
| chr7:129321839
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.364-57799G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321839 | ||||||
| chr7:129321864
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.364-57774C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321864 | ||||||
| chr7:129321991
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-57647G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129321991 | ||||||
| chr7:129322109
|
T | TTG | 12 | a0001c0001t0004g0158a0001c0002t0001g0265a0001c0002t0002g0188others(9): Show | 12 | HG01106.hp2 HG01243.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-57509_364-5750 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129322109 | |||||
| chr7:129322109
|
TTG | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 137 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.364-57509_364-5750 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129322109 | |||||
| chr7:129322172
|
C | T | 24 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-57466C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322172 | ||||||
| chr7:129322174
|
C | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-57464C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322174 | ||||||
| chr7:129322183
|
AGGCTGGA others(7): Show |
A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-57451_364-5743 others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129322183 | |||||
| chr7:129322202
|
T | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-57436T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322202 | ||||||
| chr7:129322327
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-57311G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322327 | ||||||
| chr7:129322355
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-57283G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322355 | ||||||
| chr7:129322384
|
C | G | 2 | a0001c0002t0002g0204a0001c0002t0002g0249 | 2 | HG01433.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.364-57254C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322384 | ||||||
| chr7:129322420
|
G | GTGAGC | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.364-57218_364-5721 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322420 | ||||||
| chr7:129322672
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.364-56966G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322672 | ||||||
| chr7:129322815
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.364-56823C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322815 | ||||||
| chr7:129322961
|
T | C | 1 | a0001c0001t0006g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-56677T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129322961 | ||||||
| chr7:129323003
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.364-56635A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323003 | ||||||
| chr7:129323210
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-56428G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323210 | ||||||
| chr7:129323421
|
C | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-56217C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323421 | ||||||
| chr7:129323574
|
T | C | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-56064T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323574 | ||||||
| chr7:129323608
|
TC | T | 14 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-56028delC | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129323608 | |||||
| chr7:129323667
|
A | G | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.364-55971A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323667 | ||||||
| chr7:129323873
|
C | CT | 89 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.364-55748dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129323873 | |||||
| chr7:129323995
|
C | T | 7 | a0001c0002t0001g0203a0001c0002t0002g0192a0001c0002t0002g0216others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-55643C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129323995 | ||||||
| chr7:129324019
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-55619C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324019 | ||||||
| chr7:129324042
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.364-55596T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324042 | ||||||
| chr7:129324059
|
C | CGTAGATT others(2): Show |
253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-55569_364-5556 others(13): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129324059 | |||||
| chr7:129324130
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-55508G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324130 | ||||||
| chr7:129324308
|
G | C | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.364-55330G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324308 | ||||||
| chr7:129324617
|
G | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-55021G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324617 | ||||||
| chr7:129324704
|
A | G | 5 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(2): Show | 5 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-54934A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324704 | ||||||
| chr7:129324717
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-54921G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324717 | ||||||
| chr7:129324946
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-54692A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324946 | ||||||
| chr7:129324990
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-54648A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129324990 | ||||||
| chr7:129325068
|
G | A | 2 | a0001c0001t0014g0067a0001c0001t0017g0066 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.364-54570G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325068 | ||||||
| chr7:129325197
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-54441G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325197 | ||||||
| chr7:129325326
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-54312C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325326 | ||||||
| chr7:129325327
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.364-54311G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325327 | ||||||
| chr7:129325409
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-54229T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325409 | ||||||
| chr7:129325511
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-54127T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325511 | ||||||
| chr7:129325606
|
C | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-54032C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325606 | ||||||
| chr7:129325778
|
G | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-53860G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325778 | ||||||
| chr7:129325834
|
T | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-53804T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325834 | ||||||
| chr7:129325852
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.364-53786C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325852 | ||||||
| chr7:129325894
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-53744G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325894 | ||||||
| chr7:129325895
|
G | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-53743G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129325895 | ||||||
| chr7:129326016
|
A | G | 1 | a0001c0002t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.364-53622A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326016 | ||||||
| chr7:129326418
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.364-53220T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326418 | ||||||
| chr7:129326508
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.364-53130A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326508 | ||||||
| chr7:129326517
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG00673.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-53121C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326517 | ||||||
| chr7:129326523
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.364-53115C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326523 | ||||||
| chr7:129326687
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-52951G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326687 | ||||||
| chr7:129326690
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-52948A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326690 | ||||||
| chr7:129326693
|
C | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.364-52945C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326693 | ||||||
| chr7:129326808
|
G | C | 1 | a0001c0002t0003g0225 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.364-52830G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326808 | ||||||
| chr7:129326939
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364-52699G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129326939 | ||||||
| chr7:129327150
|
G | A | 1 | a0001c0001t0002g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.364-52488G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327150 | ||||||
| chr7:129327171
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-52467T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327171 | ||||||
| chr7:129327410
|
G | C | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-52228G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327410 | ||||||
| chr7:129327666
|
A | G | 2 | a0001c0001t0016g0121a0001c0001t0016g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.364-51972A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327666 | ||||||
| chr7:129327782
|
A | C | 1 | a0001c0002t0003g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.364-51856A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327782 | ||||||
| chr7:129327843
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-51795T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327843 | ||||||
| chr7:129327845
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.364-51793G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327845 | ||||||
| chr7:129327892
|
C | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-51746C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129327892 | ||||||
| chr7:129328039
|
C | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-51599C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129328039 | ||||||
| chr7:129328126
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-51512A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129328126 | ||||||
| chr7:129328730
|
C | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-50908C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129328730 | ||||||
| chr7:129328766
|
A | G | 1 | a0001c0002t0002g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-50872A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129328766 | ||||||
| chr7:129328830
|
T | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-50808T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129328830 | ||||||
| chr7:129329260
|
G | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-50378G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129329260 | ||||||
| chr7:129329337
|
T | C | 25 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0122others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.364-50301T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129329337 | ||||||
| chr7:129329797
|
T | C | 1 | a0001c0001t0025g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.364-49841T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129329797 | ||||||
| chr7:129329844
|
T | C | 4 | a0001c0002t0002g0200a0001c0002t0002g0212a0001c0002t0002g0251others(1): Show | 4 | HG01243.hp1 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-49794T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129329844 | ||||||
| chr7:129329953
|
A | G | 1 | a0001c0002t0003g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.364-49685A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129329953 | ||||||
| chr7:129330047
|
G | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.364-49591G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330047 | ||||||
| chr7:129330159
|
G | A | 14 | a0001c0002t0003g0194a0001c0002t0003g0208a0001c0002t0003g0210others(11): Show | 14 | HG00423.hp2 NA18747.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-49479G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330159 | ||||||
| chr7:129330187
|
A | C | 5 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(2): Show | 5 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-49451A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330187 | ||||||
| chr7:129330328
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364-49310A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330328 | ||||||
| chr7:129330470
|
A | AT | 13 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0108others(10): Show | 13 | HG01081.hp1 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-49150dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129330470 | |||||
| chr7:129330470
|
AT | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0097others(5): Show | 8 | HG01123.hp2 HG01993.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-49150delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129330470 | |||||
| chr7:129330520
|
G | C | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-49118G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330520 | ||||||
| chr7:129330546
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-49092C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330546 | ||||||
| chr7:129330707
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-48931C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330707 | ||||||
| chr7:129330930
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.364-48708C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129330930 | ||||||
| chr7:129331181
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-48457C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331181 | ||||||
| chr7:129331289
|
C | T | 109 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.364-48349C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331289 | ||||||
| chr7:129331432
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-48206G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331432 | ||||||
| chr7:129331564
|
C | T | 1 | a0001c0002t0003g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.364-48074C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331564 | ||||||
| chr7:129331679
|
T | TAAAAATA others(176): Show |
1 | a0001c0002t0003g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.364-47946_364-4794 others(187): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(178): Show |
1 | a0001c0002t0003g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.364-47946_364-4794 others(189): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(192): Show |
5 | a0001c0002t0003g0206a0001c0002t0003g0207a0001c0002t0003g0245others(2): Show | 5 | HG02004.hp1 HG02293.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-47946_364-4794 others(203): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(193): Show |
1 | a0001c0002t0003g0242 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.364-47946_364-4794 others(204): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(200): Show |
1 | a0001c0002t0003g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.364-47946_364-4794 others(211): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(204): Show |
3 | a0001c0002t0003g0210a0001c0002t0003g0224a0001c0002t0004g0236 | 3 | HG00423.hp2 NA18970.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.364-47946_364-4794 others(215): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(205): Show |
6 | a0001c0002t0003g0194a0001c0002t0003g0223a0001c0002t0003g0227others(3): Show | 6 | NA18943.hp1 NA18966.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-47946_364-4794 others(216): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(206): Show |
1 | a0001c0002t0003g0232 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.364-47946_364-4794 others(217): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(210): Show |
2 | a0001c0002t0003g0234a0001c0002t0003g0243 | 2 | NA18994.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.364-47946_364-4794 others(221): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(211): Show |
1 | a0001c0002t0003g0230 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.364-47946_364-4794 others(222): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(213): Show |
1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364-47946_364-4794 others(224): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(224): Show |
1 | a0001c0002t0003g0231 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.364-47946_364-4794 others(235): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331679
|
T | TAAAAATA others(206): Show |
1 | a0001c0002t0003g0220 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.364-47946_364-4794 others(217): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331679 | |||||
| chr7:129331766
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-47872C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331766 | ||||||
| chr7:129331850
|
A | T | 6 | a0001c0001t0001g0025a0001c0001t0002g0123a0001c0001t0007g0285others(3): Show | 6 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-47788A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331850 | ||||||
| chr7:129331863
|
TA | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-47769delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129331863 | |||||
| chr7:129331868
|
A | T | 2 | a0001c0001t0014g0068a0001c0001t0027g0045 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.364-47770A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331868 | ||||||
| chr7:129331870
|
T | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.364-47768T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331870 | ||||||
| chr7:129331930
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.364-47708T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129331930 | ||||||
| chr7:129332361
|
G | A | 1 | a0001c0002t0003g0209 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.364-47277G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129332361 | ||||||
| chr7:129332374
|
C | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-47264C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129332374 | ||||||
| chr7:129332566
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.364-47072A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129332566 | ||||||
| chr7:129332665
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-46973A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129332665 | ||||||
| chr7:129332875
|
G | C | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-46763G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129332875 | ||||||
| chr7:129333187
|
G | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-46451G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333187 | ||||||
| chr7:129333290
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-46348C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333290 | ||||||
| chr7:129333308
|
C | CA | 35 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0094others(32): Show | 35 | HG00597.hp1 HG01069.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.364-46308dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129333308 | |||||
| chr7:129333308
|
CA | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0093a0001c0001t0002g0281others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-46308delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129333308 | |||||
| chr7:129333341
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-46297A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333341 | ||||||
| chr7:129333471
|
G | A | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-46167G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333471 | ||||||
| chr7:129333605
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.364-46033A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333605 | ||||||
| chr7:129333858
|
A | T | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-45780A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129333858 | ||||||
| chr7:129334045
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0002g0049 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.364-45593A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129334045 | ||||||
| chr7:129334220
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.364-45418G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129334220 | ||||||
| chr7:129334404
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-45234A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129334404 | ||||||
| chr7:129334535
|
T | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-45103T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129334535 | ||||||
| chr7:129334829
|
G | A | 22 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-44809G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129334829 | ||||||
| chr7:129335053
|
T | A | 2 | a0001c0001t0002g0047a0001c0001t0002g0053 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364-44585T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335053 | ||||||
| chr7:129335229
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-44409C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335229 | ||||||
| chr7:129335373
|
T | TA | 10 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0003g0148others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-44249dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129335373 | |||||
| chr7:129335570
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-44068A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335570 | ||||||
| chr7:129335750
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-43888G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335750 | ||||||
| chr7:129335852
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-43786G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335852 | ||||||
| chr7:129335858
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-43780G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335858 | ||||||
| chr7:129335908
|
C | T | 1 | a0001c0002t0003g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364-43730C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129335908 | ||||||
| chr7:129336020
|
G | GTTTCT | 5 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(2): Show | 5 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-43602_364-4359 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129336020 | |||||
| chr7:129336031
|
TTTCTTTT others(8): Show |
T | 3 | a0001c0001t0006g0117a0001c0002t0002g0188a0001c0002t0002g0198 | 3 | HG01106.hp2 HG02602.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.364-43589_364-4357 others(19): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129336031 | |||||
| chr7:129336041
|
CTTCTCTT others(3): Show |
C | 21 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-43587_364-4357 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129336041 | |||||
| chr7:129336059
|
C | T | 21 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-43579C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336059 | ||||||
| chr7:129336065
|
T | C | 21 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-43573T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336065 | ||||||
| chr7:129336069
|
TCC | T | 21 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-43568_364-4356 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336069 | ||||||
| chr7:129336071
|
C | CT | 224 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.364-43550dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129336071 | |||||
| chr7:129336071
|
C | CTT | 8 | a0001c0001t0001g0102a0001c0001t0001g0279a0001c0001t0002g0004others(5): Show | 8 | HG01168.hp2 HG02074.hp2 NA19010.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-43551_364-4355 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129336071 | |||||
| chr7:129336171
|
G | A | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.364-43467G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336171 | ||||||
| chr7:129336187
|
C | A | 1 | a0001c0002t0002g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364-43451C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336187 | ||||||
| chr7:129336482
|
A | T | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-43156A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336482 | ||||||
| chr7:129336612
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-43026G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336612 | ||||||
| chr7:129336713
|
G | C | 24 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-42925G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336713 | ||||||
| chr7:129336730
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-42908A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336730 | ||||||
| chr7:129336782
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-42856T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336782 | ||||||
| chr7:129336810
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.364-42828G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336810 | ||||||
| chr7:129336830
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.364-42808G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336830 | ||||||
| chr7:129336914
|
T | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-42724T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336914 | ||||||
| chr7:129336967
|
G | A | 2 | a0001c0001t0002g0153a0001c0001t0002g0185 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-42671G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129336967 | ||||||
| chr7:129337074
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.364-42564A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337074 | ||||||
| chr7:129337078
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-42560G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337078 | ||||||
| chr7:129337178
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-42460C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337178 | ||||||
| chr7:129337310
|
A | ATAGTTTA others(31): Show |
1 | a0001c0001t0002g0010 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.364-42325_364-4228 others(42): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129337310 | |||||
| chr7:129337493
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0002g0070 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.364-42145G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337493 | ||||||
| chr7:129337757
|
C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.364-41881C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337757 | ||||||
| chr7:129337777
|
C | T | 1 | a0001c0001t0018g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-41861C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337777 | ||||||
| chr7:129337852
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364-41786T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337852 | ||||||
| chr7:129337872
|
T | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-41766T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337872 | ||||||
| chr7:129337892
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-41746C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337892 | ||||||
| chr7:129337896
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-41742A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337896 | ||||||
| chr7:129337972
|
G | A | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.364-41666G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129337972 | ||||||
| chr7:129338034
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.364-41604G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338034 | ||||||
| chr7:129338036
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.364-41602G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338036 | ||||||
| chr7:129338076
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.364-41562A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338076 | ||||||
| chr7:129338080
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-41558C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338080 | ||||||
| chr7:129338226
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0052others(8): Show | 11 | NA18942.hp1 NA18944.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-41412A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338226 | ||||||
| chr7:129338235
|
A | T | 1 | a0001c0002t0001g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.364-41403A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338235 | ||||||
| chr7:129338605
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.364-41033T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338605 | ||||||
| chr7:129338782
|
T | G | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.364-40856T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338782 | ||||||
| chr7:129338943
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-40695T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338943 | ||||||
| chr7:129338964
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-40674C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129338964 | ||||||
| chr7:129339224
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.364-40414G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129339224 | ||||||
| chr7:129339305
|
A | G | 1 | a0001c0001t0021g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.364-40333A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129339305 | ||||||
| chr7:129339704
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.364-39934T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129339704 | ||||||
| chr7:129339916
|
C | CT | 218 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.364-39702dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129339916 | |||||
| chr7:129339916
|
C | CTT | 15 | a0001c0001t0001g0055a0001c0001t0002g0008a0001c0001t0002g0058others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-39703_364-3970 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129339916 | |||||
| chr7:129339947
|
C | A | 1 | a0001c0002t0003g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364-39691C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129339947 | ||||||
| chr7:129340075
|
C | A | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-39563C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340075 | ||||||
| chr7:129340099
|
T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0002t0003g0193others(2): Show | 5 | HG02074.hp2 NA18959.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-39539T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340099 | ||||||
| chr7:129340103
|
T | A | 1 | a0001c0001t0006g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364-39535T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340103 | ||||||
| chr7:129340123
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-39515C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340123 | ||||||
| chr7:129340126
|
G | A | 24 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-39512G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340126 | ||||||
| chr7:129340228
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.364-39410C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340228 | ||||||
| chr7:129340437
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.364-39201A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340437 | ||||||
| chr7:129340460
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-39178C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340460 | ||||||
| chr7:129340461
|
C | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-39177C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340461 | ||||||
| chr7:129340491
|
T | C | 17 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0133others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-39147T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340491 | ||||||
| chr7:129340546
|
A | C | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-39092A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340546 | ||||||
| chr7:129340567
|
C | CA | 6 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0094others(3): Show | 6 | HG03579.hp2 HG03831.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-39053dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129340567 | |||||
| chr7:129340567
|
CA | C | 7 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0002g0168others(4): Show | 7 | HG00558.hp2 HG01069.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-39053delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129340567 | |||||
| chr7:129340653
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-38985G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340653 | ||||||
| chr7:129340707
|
T | TAA | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-38931_364-3893 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340707 | ||||||
| chr7:129340749
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-38889C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340749 | ||||||
| chr7:129340752
|
T | C | 1 | a0001c0005t0024g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-38886T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340752 | ||||||
| chr7:129340964
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.364-38674A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129340964 | ||||||
| chr7:129341016
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-38622C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341016 | ||||||
| chr7:129341148
|
T | C | 1 | a0001c0002t0003g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.364-38490T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341148 | ||||||
| chr7:129341167
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.364-38471G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341167 | ||||||
| chr7:129341439
|
G | C | 10 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(7): Show | 10 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-38199G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341439 | ||||||
| chr7:129341746
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-37892C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341746 | ||||||
| chr7:129341986
|
G | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0110 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.364-37652G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129341986 | ||||||
| chr7:129342234
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-37404A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342234 | ||||||
| chr7:129342556
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0002g0009 | 2 | NA18982.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.364-37082T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342556 | ||||||
| chr7:129342705
|
T | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-36933T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342705 | ||||||
| chr7:129342727
|
T | C | 4 | a0001c0002t0001g0263a0001c0002t0003g0197a0001c0002t0003g0209others(1): Show | 4 | HG00741.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-36911T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342727 | ||||||
| chr7:129342784
|
G | T | 2 | a0001c0002t0003g0206a0001c0002t0003g0207 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.364-36854G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342784 | ||||||
| chr7:129342812
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.364-36826C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342812 | ||||||
| chr7:129342864
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.364-36774C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342864 | ||||||
| chr7:129342903
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.364-36735A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342903 | ||||||
| chr7:129342934
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-36704A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129342934 | ||||||
| chr7:129343147
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-36491C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343147 | ||||||
| chr7:129343259
|
C | T | 1 | a0001c0002t0003g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.364-36379C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343259 | ||||||
| chr7:129343380
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.364-36258T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343380 | ||||||
| chr7:129343710
|
A | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-35928A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343710 | ||||||
| chr7:129343727
|
A | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-35911A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343727 | ||||||
| chr7:129343830
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364-35808A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129343830 | ||||||
| chr7:129344022
|
T | C | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-35616T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344022 | ||||||
| chr7:129344046
|
A | G | 1 | a0001c0002t0002g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-35592A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344046 | ||||||
| chr7:129344177
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-35461T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344177 | ||||||
| chr7:129344519
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-35119C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344519 | ||||||
| chr7:129344670
|
C | A | 3 | a0001c0002t0010g0273a0001c0002t0010g0274a0001c0002t0010g0275 | 3 | HG02683.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.364-34968C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344670 | ||||||
| chr7:129344761
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-34877C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344761 | ||||||
| chr7:129344924
|
G | A | 1 | a0001c0002t0003g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.364-34714G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129344924 | ||||||
| chr7:129345093
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-34545T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345093 | ||||||
| chr7:129345115
|
A | C | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-34523A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345115 | ||||||
| chr7:129345116
|
C | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.364-34522C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345116 | ||||||
| chr7:129345581
|
T | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-34057T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345581 | ||||||
| chr7:129345855
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-33783G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345855 | ||||||
| chr7:129345883
|
G | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-33755G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345883 | ||||||
| chr7:129345921
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.364-33717T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129345921 | ||||||
| chr7:129346181
|
G | T | 1 | a0001c0002t0001g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.364-33457G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346181 | ||||||
| chr7:129346204
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-33434C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346204 | ||||||
| chr7:129346510
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-33128G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346510 | ||||||
| chr7:129346547
|
G | C | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0183 | 3 | HG01069.hp2 HG02683.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.364-33091G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346547 | ||||||
| chr7:129346580
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-33058A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346580 | ||||||
| chr7:129346678
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-32960G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346678 | ||||||
| chr7:129346864
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.364-32774G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346864 | ||||||
| chr7:129346993
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0002g0049 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.364-32645T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129346993 | ||||||
| chr7:129347214
|
CATT | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-32421_364-3241 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129347214 | |||||
| chr7:129347300
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.364-32338G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347300 | ||||||
| chr7:129347383
|
C | T | 1 | a0001c0001t0011g0290 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.364-32255C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347383 | ||||||
| chr7:129347513
|
A | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-32125A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347513 | ||||||
| chr7:129347612
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0185 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-32026T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347612 | ||||||
| chr7:129347645
|
G | T | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-31993G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347645 | ||||||
| chr7:129347677
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-31961C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347677 | ||||||
| chr7:129347761
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-31877C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347761 | ||||||
| chr7:129347800
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.364-31838A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347800 | ||||||
| chr7:129347891
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-31747G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129347891 | ||||||
| chr7:129348197
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-31441C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348197 | ||||||
| chr7:129348207
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0186 | 3 | HG00140.hp2 HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.364-31431G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348207 | ||||||
| chr7:129348398
|
C | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-31240C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348398 | ||||||
| chr7:129348400
|
C | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-31238C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348400 | ||||||
| chr7:129348402
|
C | A | 86 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(83): Show | 86 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.364-31236C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348402 | ||||||
| chr7:129348402
|
C | CA | 7 | a0001c0002t0001g0203a0001c0002t0002g0192a0001c0002t0002g0216others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-31236_364-3123 others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348402 | ||||||
| chr7:129348403
|
C | G | 2 | a0001c0001t0002g0004a0001c0001t0002g0040 | 2 | HG02004.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.364-31235C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348403 | ||||||
| chr7:129348404
|
A | C | 9 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(6): Show | 9 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-31234A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348404 | ||||||
| chr7:129348629
|
T | A | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-31009T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348629 | ||||||
| chr7:129348645
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.364-30993A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348645 | ||||||
| chr7:129348683
|
C | G | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-30955C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348683 | ||||||
| chr7:129348699
|
C | A | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.364-30939C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348699 | ||||||
| chr7:129348705
|
G | A | 1 | a0001c0001t0021g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.364-30933G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348705 | ||||||
| chr7:129348879
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.364-30759G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129348879 | ||||||
| chr7:129349021
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-30617C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349021 | ||||||
| chr7:129349058
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.364-30580C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349058 | ||||||
| chr7:129349082
|
T | A | 1 | a0001c0001t0021g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.364-30556T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349082 | ||||||
| chr7:129349297
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0087 | 2 | NA18948.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.364-30341T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349297 | ||||||
| chr7:129349315
|
T | A | 1 | a0001c0005t0024g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-30323T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349315 | ||||||
| chr7:129349409
|
G | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(38): Show | 41 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.364-30229G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349409 | ||||||
| chr7:129349468
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.364-30150dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349468 | |||||
| chr7:129349468
|
C | CAA | 83 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0044others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.364-30151_364-3015 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349468 | |||||
| chr7:129349468
|
C | CAAA | 14 | a0001c0001t0002g0153a0001c0001t0002g0185a0001c0001t0003g0142others(11): Show | 14 | HG00597.hp1 HG00741.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-30152_364-3015 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349468 | |||||
| chr7:129349468
|
CA | C | 11 | a0001c0001t0001g0115a0001c0001t0002g0133a0001c0001t0002g0134others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-30150delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349468 | |||||
| chr7:129349509
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.364-30129G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349509 | ||||||
| chr7:129349551
|
G | T | 1 | a0001c0002t0003g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.364-30087G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349551 | ||||||
| chr7:129349651
|
C | CA | 142 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0026others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.364-29966dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349651 | |||||
| chr7:129349651
|
C | CAA | 20 | a0001c0001t0001g0149a0001c0001t0002g0008a0001c0001t0002g0151others(17): Show | 20 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-29967_364-2996 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349651 | |||||
| chr7:129349651
|
C | CAAA | 6 | a0001c0001t0001g0292a0001c0001t0002g0129a0001c0001t0006g0117others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-29968_364-2996 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129349651 | |||||
| chr7:129349940
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-29698C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349940 | ||||||
| chr7:129349941
|
A | C | 4 | a0001c0001t0014g0067a0001c0001t0015g0077a0001c0001t0015g0078others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-29697A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129349941 | ||||||
| chr7:129350189
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.364-29449G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350189 | ||||||
| chr7:129350193
|
T | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-29445T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350193 | ||||||
| chr7:129350253
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.364-29385T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350253 | ||||||
| chr7:129350384
|
C | CT | 9 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 9 | HG01099.hp1 HG01168.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-29239dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129350384 | |||||
| chr7:129350425
|
A | C | 7 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(4): Show | 7 | HG01099.hp1 HG01123.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-29213A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350425 | ||||||
| chr7:129350476
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.364-29162C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350476 | ||||||
| chr7:129350583
|
C | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-29055C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350583 | ||||||
| chr7:129350606
|
C | T | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.364-29032C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350606 | ||||||
| chr7:129350714
|
CT | C | 137 | a0001c0001t0001g0055a0001c0001t0001g0071a0001c0001t0001g0115others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.364-28907delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129350714 | |||||
| chr7:129350747
|
A | G | 2 | a0001c0002t0002g0188a0001c0002t0002g0198 | 2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.364-28891A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350747 | ||||||
| chr7:129350792
|
A | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.364-28846A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350792 | ||||||
| chr7:129350876
|
G | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-28762G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350876 | ||||||
| chr7:129350983
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-28655C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129350983 | ||||||
| chr7:129351420
|
G | A | 1 | a0001c0001t0003g0162 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.364-28218G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129351420 | ||||||
| chr7:129351575
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364-28063A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129351575 | ||||||
| chr7:129351955
|
A | T | 1 | a0001c0002t0002g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.364-27683A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129351955 | ||||||
| chr7:129352037
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-27601A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352037 | ||||||
| chr7:129352043
|
AT | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.364-27585delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129352043 | |||||
| chr7:129352233
|
T | TA | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-27404dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129352233 | |||||
| chr7:129352377
|
A | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-27261A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352377 | ||||||
| chr7:129352386
|
C | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-27252C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352386 | ||||||
| chr7:129352395
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364-27243C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352395 | ||||||
| chr7:129352479
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.364-27159A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352479 | ||||||
| chr7:129352622
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-27016C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352622 | ||||||
| chr7:129352776
|
C | T | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-26862C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352776 | ||||||
| chr7:129352808
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-26830A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129352808 | ||||||
| chr7:129352937
|
C | CT | 109 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0140others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.364-26678dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129352937 | |||||
| chr7:129352937
|
CT | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.364-26678delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129352937 | |||||
| chr7:129353207
|
C | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0215 | 2 | HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.364-26431C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353207 | ||||||
| chr7:129353243
|
C | T | 3 | a0001c0001t0011g0290a0001c0001t0011g0291a0001c0001t0027g0045 | 3 | HG01123.hp2 HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.364-26395C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353243 | ||||||
| chr7:129353507
|
C | A | 3 | a0001c0001t0011g0290a0001c0001t0011g0291a0001c0001t0027g0045 | 3 | HG01123.hp2 HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.364-26131C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353507 | ||||||
| chr7:129353528
|
A | G | 1 | a0001c0001t0012g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.364-26110A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353528 | ||||||
| chr7:129353542
|
A | G | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.364-26096A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353542 | ||||||
| chr7:129353578
|
G | A | 2 | a0001c0002t0001g0267a0001c0002t0001g0269 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.364-26060G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353578 | ||||||
| chr7:129353602
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-26036G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353602 | ||||||
| chr7:129353659
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364-25979G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353659 | ||||||
| chr7:129353663
|
T | A | 1 | a0001c0001t0002g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.364-25975T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353663 | ||||||
| chr7:129353682
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-25956G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353682 | ||||||
| chr7:129353708
|
T | C | 1 | a0001c0002t0002g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364-25930T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353708 | ||||||
| chr7:129353767
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-25871A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353767 | ||||||
| chr7:129353915
|
T | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.364-25723T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353915 | ||||||
| chr7:129353965
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-25673G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129353965 | ||||||
| chr7:129354013
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.364-25625G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354013 | ||||||
| chr7:129354130
|
T | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-25508T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354130 | ||||||
| chr7:129354262
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.364-25376G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354262 | ||||||
| chr7:129354590
|
T | C | 3 | a0001c0001t0011g0290a0001c0001t0011g0291a0001c0001t0027g0045 | 3 | HG01123.hp2 HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.364-25048T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354590 | ||||||
| chr7:129354591
|
C | T | 1 | a0001c0001t0022g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.364-25047C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354591 | ||||||
| chr7:129354718
|
T | G | 4 | a0001c0001t0003g0146a0001c0001t0004g0136a0001c0001t0004g0137others(1): Show | 4 | HG01346.hp1 HG01361.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-24920T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354718 | ||||||
| chr7:129354783
|
A | C | 83 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.364-24855A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354783 | ||||||
| chr7:129354857
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-24781A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354857 | ||||||
| chr7:129354961
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-24677C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129354961 | ||||||
| chr7:129355002
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.364-24636C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355002 | ||||||
| chr7:129355015
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.364-24623A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355015 | ||||||
| chr7:129355237
|
TTGC | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.364-24400_364-2439 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355237 | ||||||
| chr7:129355309
|
T | G | 4 | a0001c0001t0014g0067a0001c0001t0015g0077a0001c0001t0015g0078others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-24329T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355309 | ||||||
| chr7:129355492
|
C | T | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-24146C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355492 | ||||||
| chr7:129355593
|
T | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-24045T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355593 | ||||||
| chr7:129355761
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-23877C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129355761 | ||||||
| chr7:129356000
|
A | C | 8 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0279others(5): Show | 8 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-23638A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129356000 | ||||||
| chr7:129356059
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.364-23579T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129356059 | ||||||
| chr7:129356427
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-23211T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129356427 | ||||||
| chr7:129356756
|
A | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-22882A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129356756 | ||||||
| chr7:129357174
|
T | C | 2 | a0001c0002t0003g0206a0001c0002t0003g0207 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.364-22464T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357174 | ||||||
| chr7:129357428
|
A | C | 2 | a0001c0002t0003g0206a0001c0002t0003g0207 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.364-22210A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357428 | ||||||
| chr7:129357473
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.364-22165G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357473 | ||||||
| chr7:129357657
|
G | A | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-21981G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357657 | ||||||
| chr7:129357750
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-21888C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357750 | ||||||
| chr7:129357759
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.364-21879C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357759 | ||||||
| chr7:129357788
|
G | A | 3 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287 | 3 | HG01099.hp1 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.364-21850G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357788 | ||||||
| chr7:129357931
|
C | T | 1 | a0001c0001t0007g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.364-21707C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357931 | ||||||
| chr7:129357933
|
CA | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0172others(3): Show | 6 | HG01099.hp2 HG01516.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-21690delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129357933 | |||||
| chr7:129357997
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-21641A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129357997 | ||||||
| chr7:129358129
|
C | T | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-21509C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129358129 | ||||||
| chr7:129358222
|
T | C | 1 | a0001c0002t0003g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.364-21416T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129358222 | ||||||
| chr7:129358316
|
C | G | 2 | a0001c0001t0015g0077a0001c0001t0015g0078 | 2 | HG02809.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.364-21322C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129358316 | ||||||
| chr7:129358401
|
C | CA | 10 | a0001c0001t0001g0015a0001c0001t0009g0089a0001c0001t0011g0290others(7): Show | 10 | HG01123.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-21226dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129358401 | |||||
| chr7:129358403
|
A | C | 19 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0108others(16): Show | 19 | HG01081.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-21235A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129358403 | ||||||
| chr7:129358908
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.364-20730A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129358908 | ||||||
| chr7:129359235
|
G | GA | 4 | a0001c0002t0001g0267a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-20396dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129359235 | |||||
| chr7:129359363
|
C | T | 1 | a0001c0002t0003g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.364-20275C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129359363 | ||||||
| chr7:129359815
|
C | T | 1 | a0001c0002t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.364-19823C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129359815 | ||||||
| chr7:129359918
|
G | A | 1 | a0001c0001t0018g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.364-19720G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129359918 | ||||||
| chr7:129360119
|
AT | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-19506delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129360119 | |||||
| chr7:129360592
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-19046G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360592 | ||||||
| chr7:129360622
|
C | T | 6 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-19016C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360622 | ||||||
| chr7:129360629
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-19009T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360629 | ||||||
| chr7:129360781
|
G | C | 1 | a0001c0001t0022g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.364-18857G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360781 | ||||||
| chr7:129360926
|
G | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-18712G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360926 | ||||||
| chr7:129360930
|
T | G | 2 | a0001c0001t0001g0179a0001c0002t0002g0218 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.364-18708T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360930 | ||||||
| chr7:129360943
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.364-18695G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129360943 | ||||||
| chr7:129361106
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.364-18532C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361106 | ||||||
| chr7:129361186
|
G | T | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.364-18452G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361186 | ||||||
| chr7:129361293
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.364-18345G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361293 | ||||||
| chr7:129361332
|
T | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.364-18306T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361332 | ||||||
| chr7:129361369
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-18269C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361369 | ||||||
| chr7:129361566
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-18072T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361566 | ||||||
| chr7:129361667
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(129): Show | 132 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.364-17971A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361667 | ||||||
| chr7:129361723
|
G | A | 1 | a0001c0002t0003g0228 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.364-17915G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129361723 | ||||||
| chr7:129361792
|
AT | A | 26 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0138others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-17832delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129361792 | |||||
| chr7:129362020
|
A | T | 1 | a0001c0002t0003g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.364-17618A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362020 | ||||||
| chr7:129362026
|
C | T | 1 | a0001c0002t0003g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.364-17612C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362026 | ||||||
| chr7:129362095
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-17543C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362095 | ||||||
| chr7:129362119
|
A | G | 16 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-17519A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362119 | ||||||
| chr7:129362167
|
T | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(41): Show | 44 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.364-17471T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362167 | ||||||
| chr7:129362275
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-17363A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362275 | ||||||
| chr7:129362370
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.364-17268T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362370 | ||||||
| chr7:129362413
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364-17225C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362413 | ||||||
| chr7:129362488
|
G | C | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.364-17150G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362488 | ||||||
| chr7:129362572
|
C | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-17066C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362572 | ||||||
| chr7:129362597
|
G | GT | 30 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0180others(27): Show | 30 | HG00735.hp1 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.364-17014dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129362597 | |||||
| chr7:129362597
|
G | GTT | 6 | a0001c0001t0001g0002a0001c0001t0002g0070a0001c0001t0003g0142others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-17015_364-1701 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129362597 | |||||
| chr7:129362597
|
GT | G | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.364-17014delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129362597 | |||||
| chr7:129362597
|
GTTT | G | 15 | a0001c0001t0001g0280a0001c0001t0002g0129a0001c0001t0006g0116others(12): Show | 15 | HG01070.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-17016_364-1701 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129362597 | |||||
| chr7:129362597
|
GTTTT | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-17017_364-1701 others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129362597 | |||||
| chr7:129362766
|
A | G | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(19): Show | 22 | HG00423.hp1 HG00597.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.364-16872A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362766 | ||||||
| chr7:129362819
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.364-16819C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362819 | ||||||
| chr7:129362908
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.364-16730G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129362908 | ||||||
| chr7:129363431
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.364-16207G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129363431 | ||||||
| chr7:129363771
|
T | G | 1 | a0001c0001t0015g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.364-15867T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129363771 | ||||||
| chr7:129363774
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-15864G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129363774 | ||||||
| chr7:129363910
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-15728T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129363910 | ||||||
| chr7:129363959
|
G | A | 7 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-15679G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129363959 | ||||||
| chr7:129364068
|
A | G | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-15570A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364068 | ||||||
| chr7:129364100
|
G | A | 76 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(73): Show | 76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.364-15538G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364100 | ||||||
| chr7:129364186
|
T | A | 1 | a0001c0001t0003g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364-15452T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364186 | ||||||
| chr7:129364213
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.364-15425G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364213 | ||||||
| chr7:129364356
|
G | A | 2 | a0001c0002t0001g0196a0001c0002t0001g0265 | 2 | HG01993.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.364-15282G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364356 | ||||||
| chr7:129364391
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0102 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.364-15247A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364391 | ||||||
| chr7:129364394
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.364-15244A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364394 | ||||||
| chr7:129364410
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-15228C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364410 | ||||||
| chr7:129364436
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(138): Show | 141 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.364-15202A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364436 | ||||||
| chr7:129364581
|
G | C | 22 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-15057G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364581 | ||||||
| chr7:129364807
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.364-14831T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364807 | ||||||
| chr7:129364821
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.364-14817A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364821 | ||||||
| chr7:129364860
|
T | C | 7 | a0001c0001t0002g0129a0001c0001t0006g0116a0001c0001t0006g0117others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-14778T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364860 | ||||||
| chr7:129364896
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-14742T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129364896 | ||||||
| chr7:129365006
|
C | T | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-14632C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129365006 | ||||||
| chr7:129365480
|
T | G | 3 | a0001c0002t0003g0237a0001c0002t0003g0238a0001c0002t0003g0239 | 3 | NA18952.hp1 NA18955.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.364-14158T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129365480 | ||||||
| chr7:129365628
|
G | A | 6 | a0001c0001t0003g0159a0001c0001t0003g0162a0001c0001t0004g0158others(3): Show | 6 | HG02135.hp2 NA18944.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-14010G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129365628 | ||||||
| chr7:129365628
|
G | GTA | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-13994_364-1399 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.364-14002_364-1399 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0029a0001c0001t0002g0034 | 2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.364-14004_364-1399 others(16): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0002t0001g0196 | 3 | HG02723.hp2 HG02896.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.364-14006_364-1399 others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(9): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0279a0001c0001t0001g0280others(2): Show | 5 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-14008_364-1399 others(20): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(11): Show |
25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(22): Show | 25 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(22): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(13): Show |
24 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0065others(21): Show | 24 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(24): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(15): Show |
7 | a0001c0001t0001g0056a0001c0001t0001g0072a0001c0001t0001g0105others(4): Show | 7 | HG01168.hp1 HG01515.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(26): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(17): Show |
4 | a0001c0001t0001g0026a0001c0001t0002g0040a0001c0001t0005g0051others(1): Show | 4 | HG01952.hp2 HG02004.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(28): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(19): Show |
2 | a0001c0001t0001g0057a0001c0001t0017g0066 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.364-13993_364-1399 others(30): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(21): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0002g0027others(2): Show | 5 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(32): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0002g0070a0001c0001t0002g0282 | 2 | HG01891.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.364-13993_364-1399 others(34): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(25): Show |
1 | a0001c0001t0001g0076 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.364-13993_364-1399 others(36): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(27): Show |
5 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0083others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(38): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(29): Show |
8 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0104others(5): Show | 8 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(40): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(31): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0002g0011others(5): Show | 8 | HG01433.hp1 HG02273.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(42): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(33): Show |
6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0020others(3): Show | 6 | HG00597.hp2 HG01346.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(44): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(35): Show |
3 | a0001c0001t0001g0030a0001c0001t0002g0014a0001c0001t0002g0021 | 3 | HG02300.hp2 NA18966.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.364-13993_364-1399 others(46): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(37): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0036others(4): Show | 7 | HG01099.hp1 HG02074.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(48): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(39): Show |
3 | a0001c0001t0001g0012a0001c0001t0002g0023a0001c0001t0015g0078 | 3 | HG00423.hp1 HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.364-13993_364-1399 others(50): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(41): Show |
4 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0094others(1): Show | 4 | HG06807.hp2 NA18747.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-13993_364-1399 others(52): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(43): Show |
2 | a0001c0001t0001g0019a0001c0001t0002g0110 | 2 | NA18989.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.364-13993_364-1399 others(54): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(45): Show |
1 | a0001c0002t0002g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364-13993_364-1399 others(56): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(49): Show |
1 | a0001c0001t0006g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-13993_364-1399 others(60): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365628
|
G | GTATATAT others(57): Show |
1 | a0001c0001t0002g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364-13993_364-1399 others(68): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365628 | |||||
| chr7:129365640
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.364-13993_364-1399 others(54): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129365640 | |||||
| chr7:129365894
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.364-13744G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129365894 | ||||||
| chr7:129366027
|
A | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.364-13611A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366027 | ||||||
| chr7:129366208
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-13430T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366208 | ||||||
| chr7:129366361
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 136 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.364-13277A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366361 | ||||||
| chr7:129366505
|
G | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-13133G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366505 | ||||||
| chr7:129366633
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.364-13005G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366633 | ||||||
| chr7:129366669
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.364-12969G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366669 | ||||||
| chr7:129366770
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.364-12868C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366770 | ||||||
| chr7:129366776
|
C | CA | 273 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.364-12846dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129366776 | |||||
| chr7:129366776
|
C | CAA | 10 | a0001c0001t0001g0069a0001c0001t0002g0070a0001c0001t0002g0129others(7): Show | 10 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-12847_364-1284 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129366776 | |||||
| chr7:129366809
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.364-12829T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129366809 | ||||||
| chr7:129367071
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364-12567A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367071 | ||||||
| chr7:129367122
|
G | A | 1 | a0001c0002t0003g0209 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.364-12516G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367122 | ||||||
| chr7:129367408
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.364-12230G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367408 | ||||||
| chr7:129367424
|
T | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0049 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.364-12214T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367424 | ||||||
| chr7:129367505
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.364-12133C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367505 | ||||||
| chr7:129367739
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364-11899T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367739 | ||||||
| chr7:129367979
|
C | T | 15 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-11659C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129367979 | ||||||
| chr7:129368027
|
C | T | 1 | a0001c0001t0004g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.364-11611C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368027 | ||||||
| chr7:129368073
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-11565G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368073 | ||||||
| chr7:129368173
|
G | A | 1 | a0001c0001t0008g0150 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.364-11465G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368173 | ||||||
| chr7:129368272
|
A | C | 1 | a0001c0002t0003g0259 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.364-11366A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368272 | ||||||
| chr7:129368423
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.364-11215C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368423 | ||||||
| chr7:129368918
|
T | C | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.364-10720T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368918 | ||||||
| chr7:129368932
|
A | C | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.364-10706A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129368932 | ||||||
| chr7:129369037
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.364-10601T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369037 | ||||||
| chr7:129369059
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0052others(8): Show | 11 | NA18942.hp1 NA18944.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-10579A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369059 | ||||||
| chr7:129369215
|
T | TTTTAA | 142 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.364-10422_364-1041 others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129369215 | |||||
| chr7:129369317
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-10321C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369317 | ||||||
| chr7:129369428
|
G | T | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.364-10210G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369428 | ||||||
| chr7:129369550
|
G | GT | 30 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0055others(27): Show | 30 | HG00423.hp1 HG01123.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-10068dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129369550 | |||||
| chr7:129369550
|
GT | G | 8 | a0001c0001t0001g0138a0001c0001t0002g0176a0001c0001t0012g0120others(5): Show | 8 | HG01496.hp2 HG01891.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-10068delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129369550 | |||||
| chr7:129369550
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.364-10077_364-1006 others(14): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129369550 | |||||
| chr7:129369560
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-10078T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369560 | ||||||
| chr7:129369846
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.364-9792T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129369846 | ||||||
| chr7:129370177
|
G | A | 26 | a0001c0001t0003g0139a0001c0001t0003g0142a0001c0001t0003g0143others(23): Show | 26 | HG00673.hp2 HG01081.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-9461G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370177 | ||||||
| chr7:129370303
|
A | T | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-9335A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370303 | ||||||
| chr7:129370334
|
T | G | 3 | a0001c0001t0003g0139a0001c0001t0003g0156a0001c0001t0003g0187 | 3 | NA18959.hp1 NA18982.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.364-9304T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370334 | ||||||
| chr7:129370384
|
T | C | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-9254T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370384 | ||||||
| chr7:129370400
|
A | ATTGGTTG | 149 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.364-9238_364-9237i others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370400 | ||||||
| chr7:129370401
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.364-9237A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370401 | ||||||
| chr7:129370418
|
C | T | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-9220C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370418 | ||||||
| chr7:129370422
|
T | C | 87 | a0001c0001t0001g0057a0001c0001t0001g0138a0001c0001t0001g0140others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.364-9216T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370422 | ||||||
| chr7:129370424
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0053 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364-9214C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370424 | ||||||
| chr7:129370465
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.364-9173A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370465 | ||||||
| chr7:129370466
|
G | A | 53 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0140others(50): Show | 53 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.364-9172G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370466 | ||||||
| chr7:129370494
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.364-9144C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370494 | ||||||
| chr7:129370495
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.364-9143A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370495 | ||||||
| chr7:129370499
|
T | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.364-9139T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370499 | ||||||
| chr7:129370502
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.364-9136T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370502 | ||||||
| chr7:129370503
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.364-9135C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370503 | ||||||
| chr7:129370505
|
T | C | 56 | a0001c0001t0001g0048a0001c0001t0001g0080a0001c0001t0001g0086others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.364-9133T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370505 | ||||||
| chr7:129370515
|
A | G | 2 | a0001c0001t0004g0144a0001c0001t0004g0166 | 2 | HG03831.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.364-9123A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370515 | ||||||
| chr7:129370525
|
G | C | 14 | a0001c0001t0002g0129a0001c0002t0001g0203a0001c0002t0001g0263others(11): Show | 14 | HG00741.hp2 HG01258.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.364-9113G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370525 | ||||||
| chr7:129370525
|
G | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0065others(3): Show | 6 | NA18906.hp1 NA18950.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-9113G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370525 | ||||||
| chr7:129370526
|
G | A | 8 | a0001c0001t0002g0129a0001c0002t0001g0203a0001c0002t0002g0192others(5): Show | 8 | HG02451.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-9112G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370526 | ||||||
| chr7:129370528
|
C | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0065others(2): Show | 5 | NA18950.hp2 NA18974.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-9110C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370528 | ||||||
| chr7:129370542
|
C | CA | 7 | a0001c0001t0002g0185a0001c0001t0006g0116a0001c0001t0006g0117others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-9090dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129370542 | |||||
| chr7:129370585
|
C | G | 1 | a0001c0002t0002g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.364-9053C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370585 | ||||||
| chr7:129370612
|
A | G | 3 | a0001c0001t0002g0167a0001c0001t0014g0068a0001c0001t0026g0152 | 3 | HG03453.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.364-9026A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370612 | ||||||
| chr7:129370615
|
A | G | 2 | a0001c0001t0026g0152a0001c0002t0001g0190 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.364-9023A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370615 | ||||||
| chr7:129370622
|
C | G | 2 | a0001c0001t0011g0290a0001c0001t0011g0291 | 2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-9016C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370622 | ||||||
| chr7:129370630
|
A | G | 3 | a0001c0001t0027g0045a0001c0002t0003g0240a0001c0002t0003g0241 | 3 | HG03098.hp1 NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.364-9008A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370630 | ||||||
| chr7:129370637
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-9001A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370637 | ||||||
| chr7:129370682
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.364-8956G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370682 | ||||||
| chr7:129370951
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0186 | 3 | HG00140.hp2 HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.364-8687T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370951 | ||||||
| chr7:129370973
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.364-8665A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370973 | ||||||
| chr7:129370974
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-8664G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129370974 | ||||||
| chr7:129371006
|
A | C | 91 | a0001c0001t0001g0012a0001c0001t0002g0003a0001c0001t0002g0004others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.364-8632A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371006 | ||||||
| chr7:129371017
|
C | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-8621C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371017 | ||||||
| chr7:129371022
|
C | T | 28 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-8616C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371022 | ||||||
| chr7:129371033
|
C | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-8605C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371033 | ||||||
| chr7:129371048
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364-8590G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371048 | ||||||
| chr7:129371175
|
G | T | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.364-8463G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371175 | ||||||
| chr7:129371176
|
T | G | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.364-8462T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371176 | ||||||
| chr7:129371270
|
A | G | 5 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-8368A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371270 | ||||||
| chr7:129371365
|
A | G | 5 | a0001c0001t0003g0146a0001c0001t0004g0007a0001c0001t0004g0136others(2): Show | 5 | HG01346.hp1 HG01361.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-8273A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129371365 | ||||||
| chr7:129372165
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0002g0151 | 2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.364-7473A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372165 | ||||||
| chr7:129372207
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.364-7431C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372207 | ||||||
| chr7:129372220
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364-7418A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372220 | ||||||
| chr7:129372238
|
A | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-7400A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372238 | ||||||
| chr7:129372527
|
G | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.364-7111G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372527 | ||||||
| chr7:129372696
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-6942C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372696 | ||||||
| chr7:129372706
|
C | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.364-6932C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372706 | ||||||
| chr7:129372818
|
C | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.364-6820C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372818 | ||||||
| chr7:129372851
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-6787T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372851 | ||||||
| chr7:129372922
|
A | G | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364-6716A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129372922 | ||||||
| chr7:129373102
|
T | A | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.364-6536T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373102 | ||||||
| chr7:129373113
|
A | T | 1 | a0001c0002t0017g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364-6525A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373113 | ||||||
| chr7:129373132
|
C | T | 1 | a0001c0001t0012g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.364-6506C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373132 | ||||||
| chr7:129373267
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.364-6371T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373267 | ||||||
| chr7:129373320
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG03225.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.364-6318C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373320 | ||||||
| chr7:129373416
|
TA | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-6214delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129373416 | |||||
| chr7:129373459
|
G | A | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.364-6179G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373459 | ||||||
| chr7:129373493
|
G | A | 1 | a0001c0002t0002g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.364-6145G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129373493 | ||||||
| chr7:129373599
|
C | CA | 8 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0094others(5): Show | 8 | HG00323.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-6028dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129373599 | |||||
| chr7:129374058
|
A | C | 1 | a0001c0001t0003g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.364-5580A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374058 | ||||||
| chr7:129374352
|
A | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-5286A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374352 | ||||||
| chr7:129374403
|
C | T | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-5235C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374403 | ||||||
| chr7:129374465
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.364-5173A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374465 | ||||||
| chr7:129374523
|
G | T | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-5115G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374523 | ||||||
| chr7:129374535
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364-5103C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374535 | ||||||
| chr7:129374536
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(210): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.364-5102A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374536 | ||||||
| chr7:129374732
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364-4906G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374732 | ||||||
| chr7:129374755
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.364-4883C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129374755 | ||||||
| chr7:129374807
|
C | CA | 38 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0088others(35): Show | 38 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.364-4813dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129374807 | |||||
| chr7:129374865
|
C | CT | 8 | a0001c0001t0002g0185a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-4759dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129374865 | |||||
| chr7:129374865
|
CT | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG01167.hp2 HG01257.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-4759delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129374865 | |||||
| chr7:129375178
|
A | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-4460A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375178 | ||||||
| chr7:129375310
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-4328C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375310 | ||||||
| chr7:129375331
|
AT | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.364-4298delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129375331 | |||||
| chr7:129375428
|
A | G | 28 | a0001c0001t0003g0139a0001c0001t0003g0142a0001c0001t0003g0143others(25): Show | 28 | HG00673.hp2 HG01081.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-4210A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375428 | ||||||
| chr7:129375656
|
C | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-3982C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375656 | ||||||
| chr7:129375670
|
G | A | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.364-3968G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375670 | ||||||
| chr7:129375976
|
T | C | 1 | a0001c0001t0002g0004 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.364-3662T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129375976 | ||||||
| chr7:129376053
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-3585C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376053 | ||||||
| chr7:129376211
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.364-3427T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376211 | ||||||
| chr7:129376340
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-3298C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376340 | ||||||
| chr7:129376722
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.364-2916G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376722 | ||||||
| chr7:129376803
|
A | C | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.364-2835A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376803 | ||||||
| chr7:129376971
|
A | G | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-2667A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129376971 | ||||||
| chr7:129377502
|
C | T | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.364-2136C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129377502 | ||||||
| chr7:129377569
|
A | G | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364-2069A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129377569 | ||||||
| chr7:129378309
|
T | TA | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.364-1316dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129378309 | |||||
| chr7:129378407
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-1231G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129378407 | ||||||
| chr7:129378408
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364-1230A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129378408 | ||||||
| chr7:129378695
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.364-943A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129378695 | ||||||
| chr7:129378879
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-759T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129378879 | ||||||
| chr7:129379235
|
G | T | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.364-403G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129379235 | ||||||
| chr7:129379279
|
C | CA | 13 | a0001c0001t0001g0071a0001c0001t0001g0096a0001c0001t0001g0098others(10): Show | 13 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-342dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 129379279 | |||||
| chr7:129379300
|
T | A | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364-338T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129379300 | ||||||
| chr7:129379336
|
T | C | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-302T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129379336 | ||||||
| chr7:129379349
|
A | G | 1 | a0001c0001t0007g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.364-289A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129379349 | ||||||
| chr7:129379564
|
G | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0156 | 2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.364-74G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 1/16 | chr7 | 129379564 | ||||||
| chr7:129379797
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.475+48G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129379797 | ||||||
| chr7:129379895
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.475+146G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129379895 | ||||||
| chr7:129379923
|
A | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG01081.hp1 HG01168.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+174A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129379923 | ||||||
| chr7:129380061
|
C | A | 1 | a0001c0002t0002g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.475+312C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380061 | ||||||
| chr7:129380069
|
C | CT | 7 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(4): Show | 7 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.475+332dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129380069 | |||||
| chr7:129380179
|
G | C | 85 | a0001c0001t0002g0185a0001c0001t0003g0091a0001c0001t0003g0135others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.475+430G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380179 | ||||||
| chr7:129380352
|
C | T | 3 | a0001c0001t0003g0139a0001c0001t0003g0156a0001c0001t0003g0187 | 3 | NA18959.hp1 NA18982.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.475+603C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380352 | ||||||
| chr7:129380368
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.475+619C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380368 | ||||||
| chr7:129380483
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.475+734T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380483 | ||||||
| chr7:129380941
|
A | G | 2 | a0001c0001t0002g0129a0001c0002t0002g0248 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.475+1192A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380941 | ||||||
| chr7:129380984
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.475+1235T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129380984 | ||||||
| chr7:129381043
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475+1294C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129381043 | ||||||
| chr7:129381072
|
T | C | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.475+1323T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129381072 | ||||||
| chr7:129381253
|
T | C | 1 | a0001c0001t0009g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.475+1504T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129381253 | ||||||
| chr7:129382106
|
C | T | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+2357C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382106 | ||||||
| chr7:129382109
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.475+2360T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382109 | ||||||
| chr7:129382261
|
A | G | 82 | a0001c0001t0002g0185a0001c0001t0003g0091a0001c0001t0003g0135others(79): Show | 82 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.475+2512A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382261 | ||||||
| chr7:129382282
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.475+2533G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382282 | ||||||
| chr7:129382310
|
A | T | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.475+2561A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382310 | ||||||
| chr7:129382564
|
C | T | 2 | a0001c0002t0003g0195a0001c0002t0003g0235 | 2 | NA18979.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.475+2815C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382564 | ||||||
| chr7:129382591
|
C | CT | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+2850dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129382591 | |||||
| chr7:129382683
|
A | T | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+2934A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382683 | ||||||
| chr7:129382696
|
G | A | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+2947G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382696 | ||||||
| chr7:129382718
|
C | T | 2 | a0001c0002t0001g0196a0001c0002t0001g0265 | 2 | HG01993.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.475+2969C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382718 | ||||||
| chr7:129382963
|
C | G | 1 | a0001c0001t0002g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.475+3214C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129382963 | ||||||
| chr7:129383149
|
G | T | 1 | a0001c0001t0007g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.475+3400G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383149 | ||||||
| chr7:129383153
|
T | C | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+3404T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383153 | ||||||
| chr7:129383372
|
G | T | 1 | a0001c0002t0002g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.475+3623G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383372 | ||||||
| chr7:129383490
|
A | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.475+3741A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383490 | ||||||
| chr7:129383756
|
C | T | 251 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.475+4007C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383756 | ||||||
| chr7:129383765
|
C | G | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.475+4016C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383765 | ||||||
| chr7:129383786
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.475+4037G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129383786 | ||||||
| chr7:129384131
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.475+4382A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129384131 | ||||||
| chr7:129384222
|
ACATATAT others(52): Show |
A | 1 | a0001c0001t0009g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.475+4521_475+4579d others(61): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129384222 | |||||
| chr7:129384255
|
T | C | 9 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+4506T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129384255 | ||||||
| chr7:129384542
|
G | C | 14 | a0001c0002t0003g0194a0001c0002t0003g0208a0001c0002t0003g0210others(11): Show | 14 | HG00423.hp2 NA18747.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.476-4514G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129384542 | ||||||
| chr7:129384644
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.476-4412C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129384644 | ||||||
| chr7:129384964
|
A | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.476-4092A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129384964 | ||||||
| chr7:129385094
|
G | C | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.476-3962G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385094 | ||||||
| chr7:129385265
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.476-3791C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385265 | ||||||
| chr7:129385427
|
G | T | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.476-3629G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385427 | ||||||
| chr7:129385468
|
G | T | 36 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0048others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.476-3588G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385468 | ||||||
| chr7:129385520
|
A | G | 1 | a0001c0002t0006g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.476-3536A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385520 | ||||||
| chr7:129385634
|
G | A | 1 | a0001c0002t0002g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.476-3422G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385634 | ||||||
| chr7:129385868
|
A | G | 1 | a0001c0002t0003g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.476-3188A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385868 | ||||||
| chr7:129385989
|
T | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-3067T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129385989 | ||||||
| chr7:129386163
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01168.hp1 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.476-2893G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386163 | ||||||
| chr7:129386326
|
C | G | 2 | a0001c0001t0003g0139a0001c0001t0003g0156 | 2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.476-2730C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386326 | ||||||
| chr7:129386417
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.476-2639C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386417 | ||||||
| chr7:129386462
|
C | CA | 9 | a0001c0001t0001g0019a0001c0001t0012g0114a0001c0001t0012g0120others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.476-2581dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129386462 | |||||
| chr7:129386462
|
CA | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-2581delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129386462 | |||||
| chr7:129386694
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.476-2362C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386694 | ||||||
| chr7:129386719
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.476-2337C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386719 | ||||||
| chr7:129386749
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.476-2307A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386749 | ||||||
| chr7:129386763
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.476-2293G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386763 | ||||||
| chr7:129386818
|
T | A | 2 | a0001c0002t0002g0254a0001c0002t0017g0253 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.476-2238T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129386818 | ||||||
| chr7:129387036
|
A | G | 95 | a0001c0001t0001g0057a0001c0001t0002g0185a0001c0001t0003g0091others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.476-2020A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387036 | ||||||
| chr7:129387103
|
T | C | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.476-1953T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387103 | ||||||
| chr7:129387137
|
A | ATAGC | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.476-1918_476-1915d others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129387137 | |||||
| chr7:129387167
|
G | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.476-1889G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387167 | ||||||
| chr7:129387225
|
A | G | 1 | a0001c0001t0014g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476-1831A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387225 | ||||||
| chr7:129387379
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.476-1677G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387379 | ||||||
| chr7:129387420
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0084 | 2 | HG00099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.476-1636C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387420 | ||||||
| chr7:129387536
|
T | C | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-1520T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129387536 | ||||||
| chr7:129388845
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.476-211C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129388845 | ||||||
| chr7:129388931
|
C | T | 1 | a0001c0002t0003g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.476-125C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | chr7 | 129388931 | ||||||
| chr7:129389016
|
AT | A | 80 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.476-29delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr7 | 129389016 | |||||
| chr7:129389252
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.619+53A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | chr7 | 129389252 | ||||||
| chr7:129389286
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.619+87C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | chr7 | 129389286 | ||||||
| chr7:129389384
|
T | TA | 158 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.619+203dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 129389384 | |||||
| chr7:129389384
|
TA | T | 23 | a0001c0001t0002g0129a0001c0001t0002g0176a0001c0002t0001g0203others(20): Show | 23 | HG00597.hp1 HG01106.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.619+203delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 129389384 | |||||
| chr7:129389550
|
C | T | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.620-84C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | chr7 | 129389550 | ||||||
| chr7:129389562
|
A | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG00673.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-72A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | chr7 | 129389562 | ||||||
| chr7:129389571
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02074.hp1 HG02165.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-63G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 3/16 | chr7 | 129389571 | ||||||
| chr7:129390600
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.720+866C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129390600 | ||||||
| chr7:129390689
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0022g0050 | 3 | HG02717.hp1 HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.720+955C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129390689 | ||||||
| chr7:129390820
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.720+1086C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129390820 | ||||||
| chr7:129390821
|
G | A | 21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.720+1087G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129390821 | ||||||
| chr7:129391401
|
G | T | 85 | a0001c0001t0002g0185a0001c0001t0003g0091a0001c0001t0003g0135others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.720+1667G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129391401 | ||||||
| chr7:129391411
|
T | C | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.720+1677T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129391411 | ||||||
| chr7:129391415
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 6 | HG01070.hp2 HG01074.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+1681G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129391415 | ||||||
| chr7:129391527
|
T | C | 3 | a0001c0001t0003g0182a0001c0002t0003g0237a0001c0002t0003g0247 | 3 | NA18968.hp2 NA18969.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.720+1793T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129391527 | ||||||
| chr7:129391666
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0101 | 3 | HG00558.hp2 NA18980.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.720+1932G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129391666 | ||||||
| chr7:129392017
|
A | G | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+2283A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129392017 | ||||||
| chr7:129392122
|
G | A | 14 | a0001c0001t0001g0057a0001c0001t0002g0185a0001c0001t0011g0033others(11): Show | 14 | HG01123.hp2 HG01496.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+2388G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129392122 | ||||||
| chr7:129392154
|
T | C | 9 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+2420T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129392154 | ||||||
| chr7:129392426
|
A | G | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+2692A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129392426 | ||||||
| chr7:129392967
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.720+3233C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129392967 | ||||||
| chr7:129393042
|
G | T | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.720+3308G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393042 | ||||||
| chr7:129393078
|
C | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.720+3344C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393078 | ||||||
| chr7:129393141
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | NA18977.hp2 NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.720+3407G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393141 | ||||||
| chr7:129393179
|
C | G | 95 | a0001c0001t0001g0057a0001c0001t0002g0185a0001c0001t0003g0091others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.720+3445C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393179 | ||||||
| chr7:129393202
|
A | T | 1 | a0001c0001t0002g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.720+3468A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393202 | ||||||
| chr7:129393629
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.721-3593C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393629 | ||||||
| chr7:129393672
|
C | G | 16 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG01167.hp2 HG02735.hp1 HG03490.hp2 others(13): Show |
intron_variant | MODIFIER | c.721-3550C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393672 | ||||||
| chr7:129393751
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0002g0054 | 3 | NA18942.hp1 NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.721-3471G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393751 | ||||||
| chr7:129393832
|
T | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.721-3390T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393832 | ||||||
| chr7:129393844
|
C | T | 1 | a0001c0001t0002g0034 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.721-3378C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393844 | ||||||
| chr7:129393851
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.721-3371T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393851 | ||||||
| chr7:129393876
|
A | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.721-3346A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393876 | ||||||
| chr7:129393900
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.721-3322G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393900 | ||||||
| chr7:129393994
|
T | C | 5 | a0001c0001t0003g0145a0001c0002t0003g0238a0001c0002t0003g0239others(2): Show | 5 | NA18946.hp1 NA18950.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-3228T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129393994 | ||||||
| chr7:129394002
|
T | G | 1 | a0001c0002t0002g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.721-3220T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394002 | ||||||
| chr7:129394163
|
T | C | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.721-3059T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394163 | ||||||
| chr7:129394207
|
TGCTGTGA others(7): Show |
T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-3010_721-2997d others(16): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 129394207 | |||||
| chr7:129394248
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.721-2974C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394248 | ||||||
| chr7:129394440
|
C | CT | 48 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0026others(45): Show | 48 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.721-2758dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 129394440 | |||||
| chr7:129394440
|
C | CTT | 57 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0145others(54): Show | 57 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.721-2759_721-2758d others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 129394440 | |||||
| chr7:129394440
|
C | CTTT | 6 | a0001c0002t0003g0195a0001c0002t0003g0208a0001c0002t0003g0229others(3): Show | 6 | HG04199.hp1 NA18979.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-2760_721-2758d others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 129394440 | |||||
| chr7:129394619
|
A | G | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.721-2603A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394619 | ||||||
| chr7:129394656
|
G | C | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.721-2566G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394656 | ||||||
| chr7:129394672
|
C | G | 6 | a0001c0001t0012g0114a0001c0001t0012g0131a0001c0001t0013g0118others(3): Show | 6 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-2550C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394672 | ||||||
| chr7:129394789
|
A | G | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.721-2433A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394789 | ||||||
| chr7:129394909
|
A | G | 1 | a0001c0005t0024g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.721-2313A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129394909 | ||||||
| chr7:129395252
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.721-1970C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129395252 | ||||||
| chr7:129395275
|
A | G | 1 | a0001c0001t0003g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.721-1947A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129395275 | ||||||
| chr7:129395532
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-1690G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129395532 | ||||||
| chr7:129395679
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.721-1543A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129395679 | ||||||
| chr7:129395699
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.721-1523G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129395699 | ||||||
| chr7:129396018
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG03225.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.721-1204T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396018 | ||||||
| chr7:129396315
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0110 | 2 | NA18969.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.721-907T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396315 | ||||||
| chr7:129396356
|
A | T | 1 | a0001c0002t0003g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.721-866A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396356 | ||||||
| chr7:129396507
|
C | A | 2 | a0001c0001t0003g0159a0001c0001t0003g0162 | 2 | HG02135.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.721-715C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396507 | ||||||
| chr7:129396546
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.721-676C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396546 | ||||||
| chr7:129396667
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.721-555G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396667 | ||||||
| chr7:129396721
|
G | A | 1 | a0001c0002t0003g0227 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.721-501G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396721 | ||||||
| chr7:129396830
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.721-392C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129396830 | ||||||
| chr7:129397135
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0026g0152 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.721-87T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129397135 | ||||||
| chr7:129397188
|
G | C | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.721-34G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 4/16 | chr7 | 129397188 | ||||||
| chr7:129397605
|
T | C | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.823+281T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129397605 | ||||||
| chr7:129397616
|
A | G | 1 | a0001c0002t0002g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823+292A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129397616 | ||||||
| chr7:129397716
|
G | A | 1 | a0001c0002t0006g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823+392G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129397716 | ||||||
| chr7:129398004
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.823+680T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398004 | ||||||
| chr7:129398283
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.823+959T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398283 | ||||||
| chr7:129398336
|
T | A | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823+1012T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398336 | ||||||
| chr7:129398336
|
T | TA | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+1015dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129398336 | |||||
| chr7:129398356
|
TTTTTTA | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.823+1054_823+1059d others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129398356 | |||||
| chr7:129398440
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.823+1116A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398440 | ||||||
| chr7:129398632
|
G | A | 1 | a0001c0002t0003g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.823+1308G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398632 | ||||||
| chr7:129398669
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1345G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398669 | ||||||
| chr7:129398750
|
C | T | 1 | a0001c0002t0003g0230 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.823+1426C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398750 | ||||||
| chr7:129398813
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.824-1477G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398813 | ||||||
| chr7:129398904
|
A | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1386A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398904 | ||||||
| chr7:129398982
|
G | A | 2 | a0001c0002t0003g0213a0001c0002t0003g0214 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.824-1308G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129398982 | ||||||
| chr7:129399141
|
C | CA | 71 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(68): Show | 71 | HG00423.hp1 HG01070.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.824-1126dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399141
|
C | CAA | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.824-1127_824-1126d others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399141
|
C | CAAA | 10 | a0001c0001t0001g0017a0001c0001t0001g0065a0001c0001t0001g0096others(7): Show | 10 | HG01981.hp2 HG03927.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-1128_824-1126d others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399141
|
C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.824-1126_824-1125i others(45): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399141
|
CA | C | 81 | a0001c0001t0001g0179a0001c0001t0002g0053a0001c0001t0002g0177others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.824-1126delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399141
|
CAAAAA | C | 8 | a0001c0001t0002g0185a0001c0001t0006g0116a0001c0001t0006g0117others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1130_824-1126d others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399141 | |||||
| chr7:129399175
|
G | A | 1 | a0001c0002t0003g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.824-1115G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399175 | ||||||
| chr7:129399177
|
G | A | 1 | a0001c0001t0023g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-1113G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399177 | ||||||
| chr7:129399184
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.824-1106C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399184 | ||||||
| chr7:129399191
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.824-1099G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399191 | ||||||
| chr7:129399253
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | NA18977.hp2 NA19009.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.824-1037C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399253 | ||||||
| chr7:129399273
|
C | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.824-1017C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399273 | ||||||
| chr7:129399459
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0186 | 3 | HG00140.hp2 HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.824-831G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399459 | ||||||
| chr7:129399478
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.824-812C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399478 | ||||||
| chr7:129399579
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.824-711C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399579 | ||||||
| chr7:129399717
|
T | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-573T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399717 | ||||||
| chr7:129399724
|
C | CT | 52 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0057others(49): Show | 52 | HG00099.hp1 HG00673.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.824-546dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399724 | |||||
| chr7:129399724
|
CT | C | 11 | a0001c0001t0001g0096a0001c0001t0003g0154a0001c0001t0006g0116others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-546delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr7 | 129399724 | |||||
| chr7:129399729
|
T | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-561T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399729 | ||||||
| chr7:129399760
|
C | T | 21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.824-530C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399760 | ||||||
| chr7:129399891
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.824-399T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129399891 | ||||||
| chr7:129400016
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.824-274G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129400016 | ||||||
| chr7:129400056
|
A | T | 21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.824-234A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129400056 | ||||||
| chr7:129400107
|
A | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-183A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129400107 | ||||||
| chr7:129400177
|
T | C | 25 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.824-113T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 5/16 | chr7 | 129400177 | ||||||
| chr7:129400669
|
A | G | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.918+285A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129400669 | ||||||
| chr7:129401339
|
G | GC | 81 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0104others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.918+964dupC | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 129401339 | |||||
| chr7:129401339
|
GC | G | 21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.918+964delC | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 129401339 | |||||
| chr7:129401420
|
G | A | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+1036G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129401420 | ||||||
| chr7:129402034
|
G | A | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-1345G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402034 | ||||||
| chr7:129402070
|
A | G | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-1309A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402070 | ||||||
| chr7:129402101
|
A | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.919-1278A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402101 | ||||||
| chr7:129402184
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-1195G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402184 | ||||||
| chr7:129402228
|
A | G | 2 | a0001c0001t0001g0115a0001c0002t0001g0190 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.919-1151A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402228 | ||||||
| chr7:129402352
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919-1027G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402352 | ||||||
| chr7:129402618
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.919-761C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402618 | ||||||
| chr7:129402741
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.919-638G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402741 | ||||||
| chr7:129402925
|
GATTT | G | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.919-449_919-446del others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 129402925 | |||||
| chr7:129402975
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.919-404A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129402975 | ||||||
| chr7:129403156
|
G | A | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-223G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129403156 | ||||||
| chr7:129403320
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.919-59G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 6/16 | chr7 | 129403320 | ||||||
| chr7:129403595
|
G | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+110G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403595 | ||||||
| chr7:129403638
|
C | T | 1 | a0001c0001t0025g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1025+153C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403638 | ||||||
| chr7:129403659
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0102 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1025+174C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403659 | ||||||
| chr7:129403660
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0102 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1025+175A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403660 | ||||||
| chr7:129403679
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1025+194C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403679 | ||||||
| chr7:129403848
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1025+363G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403848 | ||||||
| chr7:129403860
|
C | CA | 43 | a0001c0001t0001g0115a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 43 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1025+406dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
C | CAAAAAA | 10 | a0001c0001t0001g0138a0001c0001t0001g0172a0001c0001t0001g0180others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1025+401_1025+406d others(8): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
C | CAAAAAAA | 10 | a0001c0001t0001g0140a0001c0001t0001g0147a0001c0001t0001g0149others(7): Show | 10 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+400_1025+406d others(9): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1025+392_1025+406d others(17): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0011g0291 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1025+386_1025+406d others(23): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0011g0033a0001c0001t0011g0290 | 2 | HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+385_1025+406d others(24): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
CAAAAAAA others(1): Show |
C | 129 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1025+399_1025+406d others(10): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403860
|
CAAAAAAA others(8): Show |
C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+392_1025+406d others(17): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403860 | |||||
| chr7:129403880
|
A | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1025+395A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403880 | ||||||
| chr7:129403898
|
C | CTAT | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+413_1025+414i others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403898 | ||||||
| chr7:129403899
|
C | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+414C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403899 | ||||||
| chr7:129403900
|
T | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+415T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403900 | ||||||
| chr7:129403902
|
C | GTATGAGG others(8): Show |
3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1025+417delCinsGTA others(13): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129403902 | ||||||
| chr7:129403978
|
G | GT | 6 | a0001c0001t0001g0292a0001c0001t0002g0167a0001c0001t0003g0154others(3): Show | 6 | HG01346.hp1 HG02109.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+505dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr7 | 129403978 | |||||
| chr7:129404301
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1026-796T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404301 | ||||||
| chr7:129404503
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1026-594C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404503 | ||||||
| chr7:129404538
|
G | A | 1 | a0001c0002t0003g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1026-559G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404538 | ||||||
| chr7:129404548
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1026-549G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404548 | ||||||
| chr7:129404590
|
G | T | 1 | a0001c0001t0002g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1026-507G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404590 | ||||||
| chr7:129404665
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1026-432G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404665 | ||||||
| chr7:129404904
|
T | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-193T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129404904 | ||||||
| chr7:129405055
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1026-42A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 7/16 | chr7 | 129405055 | ||||||
| chr7:129405350
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1142+137A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405350 | ||||||
| chr7:129405381
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1142+168C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405381 | ||||||
| chr7:129405382
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1142+169C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405382 | ||||||
| chr7:129405482
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1142+269C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405482 | ||||||
| chr7:129405538
|
A | G | 1 | a0001c0002t0003g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1143-298A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405538 | ||||||
| chr7:129405828
|
T | C | 1 | a0001c0002t0002g0260 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.1143-8T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 8/16 | chr7 | 129405828 | ||||||
| chr7:129405924
|
A | G | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1206+25A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 9/16 | chr7 | 129405924 | ||||||
| chr7:129405999
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1206+100A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 9/16 | chr7 | 129405999 | ||||||
| chr7:129406050
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1206+151C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 9/16 | chr7 | 129406050 | ||||||
| chr7:129406145
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(242): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1207-233A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 9/16 | chr7 | 129406145 | ||||||
| chr7:129406358
|
G | A | 1 | a0001c0002t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1207-20G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 9/16 | chr7 | 129406358 | ||||||
| chr7:129406594
|
T | C | 1 | a0001c0002t0003g0220 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1295+128T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129406594 | ||||||
| chr7:129406988
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1295+522C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129406988 | ||||||
| chr7:129406991
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1295+525T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129406991 | ||||||
| chr7:129407135
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1295+669C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129407135 | ||||||
| chr7:129407207
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1295+741C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129407207 | ||||||
| chr7:129407527
|
A | G | 29 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(26): Show | 29 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1295+1061A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129407527 | ||||||
| chr7:129407863
|
G | A | 1 | a0001c0002t0017g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1295+1397G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129407863 | ||||||
| chr7:129408345
|
G | A | 5 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1296-1131G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408345 | ||||||
| chr7:129408744
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296-732G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408744 | ||||||
| chr7:129408748
|
AAAGGCAT others(13): Show |
A | 5 | a0001c0001t0014g0067a0001c0001t0014g0068a0001c0001t0015g0077others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296-726_1296-707d others(22): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 129408748 | |||||
| chr7:129408769
|
A | T | 5 | a0001c0001t0014g0067a0001c0001t0014g0068a0001c0001t0015g0077others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296-707A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408769 | ||||||
| chr7:129408803
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1296-673G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408803 | ||||||
| chr7:129408837
|
G | A | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296-639G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408837 | ||||||
| chr7:129408859
|
G | T | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1296-617G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129408859 | ||||||
| chr7:129409087
|
TA | T | 88 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1296-376delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 129409087 | |||||
| chr7:129409099
|
A | AC | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296-377_1296-376i others(3): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129409099 | ||||||
| chr7:129409099
|
A | C | 23 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1296-377A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129409099 | ||||||
| chr7:129409332
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1296-144G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 10/16 | chr7 | 129409332 | ||||||
| chr7:129409655
|
G | T | 6 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+109G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129409655 | ||||||
| chr7:129409666
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(240): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1366+120A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129409666 | ||||||
| chr7:129409726
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1366+180C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129409726 | ||||||
| chr7:129409852
|
A | AT | 247 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1366+316dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129409852 | |||||
| chr7:129409939
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1366+393G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129409939 | ||||||
| chr7:129410361
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1366+815G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129410361 | ||||||
| chr7:129410499
|
G | A | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1366+953G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129410499 | ||||||
| chr7:129410551
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1366+1005C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129410551 | ||||||
| chr7:129410824
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+1278G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129410824 | ||||||
| chr7:129411137
|
T | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+1591T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411137 | ||||||
| chr7:129411288
|
C | T | 2 | a0001c0002t0001g0196a0001c0002t0001g0265 | 2 | HG01993.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1366+1742C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411288 | ||||||
| chr7:129411328
|
C | T | 1 | a0001c0002t0004g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1366+1782C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411328 | ||||||
| chr7:129411378
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0035 | 2 | NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1366+1832C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411378 | ||||||
| chr7:129411437
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1366+1891G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411437 | ||||||
| chr7:129411460
|
T | A | 2 | a0001c0001t0018g0283a0001c0001t0018g0284 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1366+1914T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411460 | ||||||
| chr7:129411558
|
G | A | 1 | a0001c0005t0024g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1366+2012G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411558 | ||||||
| chr7:129411605
|
C | CA | 31 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1367-1983dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129411605 | |||||
| chr7:129411664
|
CAGG | C | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1367-1927_1367-192 others(7): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129411664 | |||||
| chr7:129411672
|
T | C | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1367-1922T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411672 | ||||||
| chr7:129411740
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1367-1854C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129411740 | ||||||
| chr7:129411759
|
C | CA | 85 | a0001c0001t0001g0057a0001c0001t0003g0091a0001c0001t0003g0135others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1367-1819dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129411759 | |||||
| chr7:129412297
|
CT | C | 20 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1367-1281delT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129412297 | |||||
| chr7:129412370
|
T | G | 31 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1367-1224T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412370 | ||||||
| chr7:129412373
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1367-1221C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412373 | ||||||
| chr7:129412540
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1367-1054C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412540 | ||||||
| chr7:129412714
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1367-880G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412714 | ||||||
| chr7:129412751
|
T | C | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1367-843T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412751 | ||||||
| chr7:129412753
|
C | A | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1367-841C>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412753 | ||||||
| chr7:129412754
|
C | T | 1 | a0001c0002t0003g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1367-840C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412754 | ||||||
| chr7:129412788
|
G | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0167a0001c0001t0018g0283others(1): Show | 4 | HG01167.hp1 HG01891.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-806G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129412788 | ||||||
| chr7:129413013
|
A | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-581A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129413013 | ||||||
| chr7:129413126
|
G | C | 1 | a0001c0001t0003g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1367-468G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129413126 | ||||||
| chr7:129413144
|
C | CT | 129 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1367-435dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129413144 | |||||
| chr7:129413144
|
C | CTT | 7 | a0001c0001t0001g0102a0001c0001t0001g0112a0001c0001t0002g0054others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367-436_1367-435d others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr7 | 129413144 | |||||
| chr7:129413251
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0022g0050 | 3 | HG02717.hp1 HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1367-343C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129413251 | ||||||
| chr7:129413381
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1367-213T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 11/16 | chr7 | 129413381 | ||||||
| chr7:129413957
|
A | G | 1 | a0001c0002t0002g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1461+269A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129413957 | ||||||
| chr7:129413980
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1461+292C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129413980 | ||||||
| chr7:129414170
|
G | T | 5 | a0001c0001t0014g0067a0001c0001t0014g0068a0001c0001t0015g0077others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461+482G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414170 | ||||||
| chr7:129414171
|
G | T | 5 | a0001c0001t0014g0067a0001c0001t0014g0068a0001c0001t0015g0077others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461+483G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414171 | ||||||
| chr7:129414314
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1461+626C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414314 | ||||||
| chr7:129414370
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1461+682C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414370 | ||||||
| chr7:129414420
|
C | CT | 17 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0008others(14): Show | 17 | HG01123.hp2 HG01167.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1461+750dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129414420 | |||||
| chr7:129414420
|
C | CTT | 193 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1461+749_1461+750d others(4): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129414420 | |||||
| chr7:129414420
|
C | CTTT | 8 | a0001c0001t0001g0103a0001c0001t0001g0279a0001c0001t0002g0046others(5): Show | 8 | HG01168.hp2 HG02055.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461+748_1461+750d others(5): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129414420 | |||||
| chr7:129414420
|
C | CTTTT | 31 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1461+747_1461+750d others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129414420 | |||||
| chr7:129414484
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1461+796G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414484 | ||||||
| chr7:129414570
|
G | A | 1 | a0001c0001t0004g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1461+882G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414570 | ||||||
| chr7:129414603
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1461+915T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414603 | ||||||
| chr7:129414623
|
A | G | 1 | a0001c0002t0002g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1461+935A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414623 | ||||||
| chr7:129414718
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1461+1030C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414718 | ||||||
| chr7:129414838
|
T | A | 1 | a0001c0001t0003g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1461+1150T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129414838 | ||||||
| chr7:129415040
|
G | A | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1461+1352G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415040 | ||||||
| chr7:129415363
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1461+1675T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415363 | ||||||
| chr7:129415396
|
T | A | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0180others(3): Show | 6 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461+1708T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415396 | ||||||
| chr7:129415407
|
T | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1461+1719T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415407 | ||||||
| chr7:129415490
|
G | T | 1 | a0001c0001t0004g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1461+1802G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415490 | ||||||
| chr7:129415551
|
G | A | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1461+1863G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415551 | ||||||
| chr7:129415639
|
A | G | 81 | a0001c0001t0003g0091a0001c0001t0003g0135a0001c0001t0003g0139others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1461+1951A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415639 | ||||||
| chr7:129415975
|
G | A | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461+2287G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129415975 | ||||||
| chr7:129416025
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1461+2337G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416025 | ||||||
| chr7:129416116
|
T | C | 6 | a0001c0001t0005g0059a0001c0001t0005g0060a0001c0001t0005g0061others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461+2428T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416116 | ||||||
| chr7:129416370
|
T | G | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0180others(3): Show | 6 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461+2682T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416370 | ||||||
| chr7:129416400
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1461+2712A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416400 | ||||||
| chr7:129416468
|
T | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0002g0278 | 3 | HG01070.hp2 HG01074.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1461+2780T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416468 | ||||||
| chr7:129416614
|
A | G | 1 | a0001c0002t0002g0276 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1461+2926A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416614 | ||||||
| chr7:129416724
|
C | T | 1 | a0001c0002t0003g0244 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1461+3036C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416724 | ||||||
| chr7:129416787
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1461+3099C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416787 | ||||||
| chr7:129416851
|
T | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1461+3163T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416851 | ||||||
| chr7:129416852
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1461+3164G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416852 | ||||||
| chr7:129416854
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1461+3166G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416854 | ||||||
| chr7:129416856
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1461+3168G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416856 | ||||||
| chr7:129416919
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1461+3231G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416919 | ||||||
| chr7:129416937
|
G | A | 7 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1461+3249G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129416937 | ||||||
| chr7:129417114
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461+3426G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417114 | ||||||
| chr7:129417723
|
A | G | 1 | a0001c0001t0018g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1461+4035A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417723 | ||||||
| chr7:129417781
|
A | G | 31 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1461+4093A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417781 | ||||||
| chr7:129417795
|
C | G | 1 | a0001c0001t0022g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1461+4107C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417795 | ||||||
| chr7:129417935
|
G | A | 7 | a0001c0001t0006g0116a0001c0001t0006g0117a0001c0001t0006g0126others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1461+4247G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417935 | ||||||
| chr7:129417971
|
A | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG00673.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1461+4283A>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129417971 | ||||||
| chr7:129418068
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1461+4380C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129418068 | ||||||
| chr7:129418391
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(250): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1462-4449T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129418391 | ||||||
| chr7:129418481
|
A | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-4359A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129418481 | ||||||
| chr7:129418599
|
G | A | 1 | a0001c0002t0003g0227 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1462-4241G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129418599 | ||||||
| chr7:129418884
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1462-3956T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129418884 | ||||||
| chr7:129419229
|
G | C | 5 | a0001c0001t0014g0067a0001c0001t0014g0068a0001c0001t0015g0077others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-3611G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419229 | ||||||
| chr7:129419266
|
A | G | 1 | a0001c0001t0005g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1462-3574A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419266 | ||||||
| chr7:129419423
|
G | A | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1462-3417G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419423 | ||||||
| chr7:129419469
|
G | T | 4 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462-3371G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419469 | ||||||
| chr7:129419549
|
G | A | 9 | a0001c0001t0002g0153a0001c0001t0012g0114a0001c0001t0012g0120others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1462-3291G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419549 | ||||||
| chr7:129419561
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1462-3279A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419561 | ||||||
| chr7:129419672
|
G | A | 4 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0254others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462-3168G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419672 | ||||||
| chr7:129419743
|
A | C | 28 | a0001c0001t0003g0139a0001c0001t0003g0142a0001c0001t0003g0143others(25): Show | 28 | HG00673.hp2 HG01081.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.1462-3097A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419743 | ||||||
| chr7:129419898
|
G | T | 1 | a0003c0004t0001g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1462-2942G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419898 | ||||||
| chr7:129419922
|
G | A | 4 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0183others(1): Show | 4 | HG01069.hp2 HG01258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462-2918G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419922 | ||||||
| chr7:129419929
|
A | G | 1 | a0001c0001t0004g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1462-2911A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419929 | ||||||
| chr7:129419958
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-2882G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129419958 | ||||||
| chr7:129420155
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1462-2685C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129420155 | ||||||
| chr7:129420172
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1462-2668T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129420172 | ||||||
| chr7:129420477
|
C | CT | 30 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0138others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1462-2344dupT | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129420477 | |||||
| chr7:129420477
|
C | CTT | 9 | a0001c0001t0001g0057a0001c0001t0012g0114a0001c0001t0012g0120others(6): Show | 9 | HG01496.hp2 HG02055.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1462-2345_1462-234 others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129420477 | |||||
| chr7:129420511
|
C | G | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-2329C>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129420511 | ||||||
| chr7:129420515
|
T | C | 3 | a0001c0001t0003g0148a0001c0002t0003g0205a0001c0002t0003g0209 | 3 | HG01515.hp1 HG01993.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1462-2325T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129420515 | ||||||
| chr7:129420545
|
T | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1462-2295T>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129420545 | ||||||
| chr7:129421251
|
C | CA | 152 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1462-1575dupA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129421251 | |||||
| chr7:129421251
|
CA | C | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-1575delA | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 129421251 | |||||
| chr7:129421591
|
A | G | 1 | a0001c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1462-1249A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129421591 | ||||||
| chr7:129421720
|
G | A | 1 | a0001c0001t0019g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1462-1120G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129421720 | ||||||
| chr7:129421870
|
A | G | 1 | a0001c0001t0007g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1462-970A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129421870 | ||||||
| chr7:129422135
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1462-705T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422135 | ||||||
| chr7:129422450
|
A | G | 2 | a0001c0002t0003g0195a0001c0002t0003g0235 | 2 | NA18979.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1462-390A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422450 | ||||||
| chr7:129422507
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1462-333A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422507 | ||||||
| chr7:129422732
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1462-108T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422732 | ||||||
| chr7:129422792
|
C | T | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1462-48C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422792 | ||||||
| chr7:129422817
|
T | C | 1 | a0001c0001t0009g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1462-23T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 12/16 | chr7 | 129422817 | ||||||
| chr7:129423256
|
C | T | 1 | a0001c0001t0027g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1560+318C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423256 | ||||||
| chr7:129423268
|
G | A | 1 | a0001c0001t0019g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1560+330G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423268 | ||||||
| chr7:129423296
|
T | C | 2 | a0001c0002t0002g0212a0001c0002t0002g0251 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1560+358T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423296 | ||||||
| chr7:129423589
|
A | G | 2 | a0001c0002t0010g0274a0001c0002t0010g0275 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1560+651A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423589 | ||||||
| chr7:129423688
|
T | C | 1 | a0001c0001t0026g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1560+750T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423688 | ||||||
| chr7:129423724
|
T | C | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1560+786T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423724 | ||||||
| chr7:129423923
|
T | C | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1561-951T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129423923 | ||||||
| chr7:129424257
|
G | A | 8 | a0001c0001t0012g0114a0001c0001t0012g0120a0001c0001t0012g0131others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1561-617G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129424257 | ||||||
| chr7:129424269
|
G | A | 2 | a0001c0001t0004g0136a0001c0001t0004g0137 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1561-605G>A | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129424269 | ||||||
| chr7:129424398
|
T | TAATC | 4 | a0001c0001t0001g0088a0001c0001t0002g0049a0001c0001t0014g0067others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1561-446_1561-443d others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 129424398 | |||||
| chr7:129424398
|
TAATC | T | 4 | a0001c0001t0001g0048a0001c0001t0002g0282a0001c0001t0004g0144others(1): Show | 4 | HG01106.hp1 HG03491.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561-446_1561-443d others(6): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 129424398 | |||||
| chr7:129424398
|
TAATCAAT others(9): Show |
T | 3 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01168.hp1 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1561-458_1561-443d others(18): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 129424398 | |||||
| chr7:129424593
|
A | G | 1 | a0001c0001t0003g0154 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1561-281A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 13/16 | chr7 | 129424593 | ||||||
| chr7:129425580
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0028 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1708+439T>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129425580 | ||||||
| chr7:129425636
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1708+495A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129425636 | ||||||
| chr7:129425830
|
G | T | 9 | a0001c0001t0002g0129a0001c0002t0002g0192a0001c0002t0002g0204others(6): Show | 9 | HG01433.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1709-613G>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129425830 | ||||||
| chr7:129425831
|
A | C | 3 | a0001c0001t0011g0033a0001c0001t0011g0290a0001c0001t0011g0291 | 3 | HG01123.hp2 HG02273.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1709-612A>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129425831 | ||||||
| chr7:129425933
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1709-510A>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129425933 | ||||||
| chr7:129426081
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1709-362G>C | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129426081 | ||||||
| chr7:129426256
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1709-187C>T | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 15/16 | chr7 | 129426256 | ||||||
| chr7:129426721
|
T | TAAATAGT others(304): Show |
1 | a0001c0001t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1829+171_1829+172i others(313): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 129426721 | |||||
| chr7:129426721
|
T | TAAATAGT others(305): Show |
22 | a0001c0001t0001g0140a0001c0001t0001g0147a0001c0001t0001g0149others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1829+171_1829+172i others(314): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 129426721 | |||||
| chr7:129426721
|
T | TAAATAGT others(306): Show |
1 | a0001c0001t0016g0121 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1829+171_1829+172i others(315): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 129426721 | |||||
| chr7:129426721
|
T | TAAATAGT others(307): Show |
6 | a0001c0001t0012g0114a0001c0001t0012g0131a0001c0001t0013g0118others(3): Show | 6 | HG02055.hp1 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1829+171_1829+172i others(316): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 129426721 | |||||
| chr7:129426721
|
T | TAAATAGT others(308): Show |
1 | a0001c0001t0012g0120 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1829+171_1829+172i others(317): Show |
AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 129426721 | |||||
| chr7:129426778
|
T | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG00673.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1829+215T>G | AHCYL2 | ENSG00000158467.17 | transcript | ENST00000325006.8 | protein_coding | 16/16 | chr7 | 129426778 |