Item | Value |
---|---|
geneid | 55183 |
ensemblid | ENSG00000080345.18 |
hgncid | 23207 |
symbol | RIF1 |
name | replication timing regulatory factor 1 |
refseq_nuc | NM_018151.5 |
refseq_prot | NP_060621.3 |
ensembl_nuc | ENST00000444746.7 |
ensembl_prot | ENSP00000390181.2 |
mane_status | MANE Select |
chr | chr2 |
start | 151409902 |
end | 151482172 |
strand | + |
ver | v1.2 |
region | chr2:151409902-151482172 |
region5000 | chr2:151404902-151487172 |
regionname0 | RIF1_chr2_151409902_151482172 |
regionname5000 | RIF1_chr2_151404902_151487172 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2472 | 206 | 20 | 40 | 113 | 11 | 21 | 88 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0002 | 1/0 | 2472 | 109 | 34 | 17 | 37 | 6 | 14 | 30 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0003 | 0/0 | 2472 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0004 | 0/0 | 2472 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0005 | 0/0 | 2472 | 6 | 4 | 0 | 0 | 1 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0006 | 0/0 | 2472 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0007 | 0/0 | 2472 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0008 | 0/0 | 2472 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0009 | 0/0 | 2472 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0010 | 0/0 | 2472 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0011 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0012 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0013 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0014 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0015 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0016 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0017 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0018 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0019 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0020 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0021 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0022 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0023 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0024 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0025 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0026 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0027 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
a0028 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | MTARG others(2467): Show |
chr2 | 151404902 | 151487172 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 7416 | 81 | 4 | 22 | 44 | 5 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0003 | 0/1 | 7416 | 75 | 7 | 15 | 39 | 6 | 7 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0004 | 0/0 | 7416 | 36 | 1 | 1 | 30 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0007 | 0/0 | 7416 | 6 | 6 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0009 | 0/0 | 7416 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0016 | 0/0 | 7416 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0022 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0001c0038 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0002c0001 | 1/0 | 7416 | 106 | 34 | 17 | 34 | 6 | 14 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0002c0013 | 0/0 | 7416 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0003c0005 | 0/0 | 7416 | 15 | 14 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0003c0019 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0004c0006 | 0/0 | 7416 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0005c0010 | 0/0 | 7416 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0005c0018 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0006c0011 | 0/0 | 7416 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0007c0012 | 0/0 | 7416 | 4 | 3 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0008c0008 | 0/0 | 7416 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0009c0014 | 0/0 | 7416 | 3 | 0 | 3 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0010c0017 | 0/0 | 7416 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0011c0015 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0012c0024 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0013c0026 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0014c0021 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0015c0036 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0016c0023 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0017c0034 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0018c0028 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0019c0033 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0020c0032 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0021c0029 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0022c0027 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0023c0020 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0024c0035 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0025c0025 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0026c0031 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0027c0030 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 | ||
a0028c0037 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | ATGAC others(7411): Show |
chr2 | 151404902 | 151487172 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 14663 | 65 | 0 | 21 | 35 | 5 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0013 | 0/0 | 14663 | 4 | 0 | 1 | 2 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0021 | 0/0 | 14663 | 2 | 0 | 0 | 2 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0025 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0032 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0045 | 0/0 | 14663 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0046 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0047 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0048 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0050 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0051 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0002t0052 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0002 | 0/0 | 14663 | 51 | 0 | 10 | 29 | 6 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0011 | 0/0 | 14659 | 5 | 0 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14654): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0024 | 0/0 | 14663 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0027 | 0/0 | 14659 | 2 | 0 | 0 | 2 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14654): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0028 | 0/0 | 14663 | 2 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0033 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0034 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0035 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0036 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0037 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0042 | 0/1 | 14663 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0054 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0055 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0056 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0057 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0058 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0003t0059 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0004t0005 | 0/0 | 14661 | 18 | 0 | 0 | 16 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0001c0004t0006 | 0/0 | 14661 | 15 | 0 | 1 | 12 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0001c0004t0041 | 0/0 | 14659 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14654): Show |
chr2 | 151404902 | 151487172 |
a0001c0004t0043 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0001c0004t0044 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0001c0007t0022 | 0/0 | 14660 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14655): Show |
chr2 | 151404902 | 151487172 |
a0001c0007t0023 | 0/0 | 14660 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14655): Show |
chr2 | 151404902 | 151487172 |
a0001c0009t0015 | 0/0 | 14660 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14655): Show |
chr2 | 151404902 | 151487172 |
a0001c0016t0002 | 0/0 | 14663 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0022t0025 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0001c0038t0030 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0003 | 1/0 | 14662 | 42 | 2 | 9 | 23 | 2 | 5 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0004 | 0/0 | 14662 | 22 | 17 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0008 | 0/0 | 14657 | 7 | 0 | 6 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14652): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0010 | 0/0 | 14661 | 6 | 6 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0012 | 0/0 | 14663 | 5 | 0 | 0 | 3 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0017 | 0/0 | 14662 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0019 | 0/0 | 14662 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0020 | 0/0 | 14662 | 3 | 0 | 0 | 0 | 1 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0026 | 0/0 | 14662 | 3 | 2 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0038 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0039 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0053 | 0/0 | 14662 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0060 | 0/0 | 14663 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0061 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0064 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0065 | 0/0 | 14661 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0066 | 0/0 | 14661 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0067 | 0/0 | 14662 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0069 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0001t0070 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0002c0013t0003 | 0/0 | 14662 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0003c0005t0007 | 0/0 | 14663 | 12 | 11 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0003c0005t0016 | 0/0 | 14663 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0003c0019t0068 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0004c0006t0009 | 0/0 | 14663 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0005c0010t0018 | 0/0 | 14663 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0005c0018t0031 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0006c0011t0014 | 0/0 | 14663 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0007c0012t0007 | 0/0 | 14663 | 4 | 3 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0008c0008t0001 | 0/0 | 14663 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0009c0014t0001 | 0/0 | 14663 | 3 | 0 | 3 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0010c0017t0002 | 0/0 | 14663 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0011c0015t0029 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0012c0024t0049 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0013c0026t0040 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0014c0021t0001 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0015c0036t0008 | 0/0 | 14657 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14652): Show |
chr2 | 151404902 | 151487172 |
a0016c0023t0001 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0017c0034t0063 | 0/0 | 14665 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14660): Show |
chr2 | 151404902 | 151487172 |
a0018c0028t0002 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0019c0033t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0020c0032t0062 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0021c0029t0030 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0022c0027t0016 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0023c0020t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0024c0035t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14657): Show |
chr2 | 151404902 | 151487172 |
a0025c0025t0001 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0026c0031t0002 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
a0027c0030t0006 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14656): Show |
chr2 | 151404902 | 151487172 |
a0028c0037t0021 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | AGCCG others(14658): Show |
chr2 | 151404902 | 151487172 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0013g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0013g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0021g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0021g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0025g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0032g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0045g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0046g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0047g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0048g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0050g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0051g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0052g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0024g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0024g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0024g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0027g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0027g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0028g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0028g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0033g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0034g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0035g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0036g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0037g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0042g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0054g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0055g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0056g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0057g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0058g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0059g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0041g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0043g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0044g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0022g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0022g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0022g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0016t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0016t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0022t0025g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0038t0030g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0012g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0017g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0017g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0020g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0020g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0020g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0038g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0039g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0053g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0060g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0061g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0064g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0065g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0066g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0067g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0069g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0070g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0019t0068g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0018g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0018g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0018g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0018t0031g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0018t0031g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0014g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0012t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0012t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0012t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0012t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0008t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0008t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0008t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0008t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0010c0017t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0010c0017t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0011c0015t0029g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0011c0015t0029g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0012c0024t0049g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0013c0026t0040g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0014c0021t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0015c0036t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0016c0023t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0017c0034t0063g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0018c0028t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0019c0033t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0020c0032t0062g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0021c0029t0030g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0022c0027t0016g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0023c0020t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0024c0035t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0025c0025t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0026c0031t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0027c0030t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0028c0037t0021g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0371 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0129 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00140 | hp1 | a0001 | c0003 | t0002 | g0174 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0303 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0335 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00280 | hp2 | a0002 | c0001 | t0053 | g0245 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00323 | hp1 | a0002 | c0001 | t0012 | g0045 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0351 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00423 | hp2 | a0006 | c0011 | t0014 | g0176 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0372 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00438 | hp2 | a0002 | c0001 | t0003 | g0238 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00544 | hp1 | a0002 | c0001 | t0003 | g0206 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00544 | hp2 | a0001 | c0004 | t0006 | g0076 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00558 | hp1 | a0001 | c0002 | t0052 | g0342 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00597 | hp1 | a0001 | c0004 | t0005 | g0084 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0049 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00609 | hp1 | a0006 | c0011 | t0014 | g0092 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00609 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0118 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00621 | hp2 | a0012 | c0024 | t0049 | g0336 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00639 | hp1 | a0003 | c0005 | t0007 | g0285 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00639 | hp2 | a0013 | c0026 | t0040 | g0051 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00642 | hp2 | a0001 | c0003 | t0002 | g0122 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00673 | hp1 | a0001 | c0004 | t0005 | g0079 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00673 | hp2 | a0002 | c0001 | t0003 | g0215 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0131 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00733 | hp2 | a0014 | c0021 | t0001 | g0345 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0136 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00738 | hp2 | a0002 | c0001 | t0003 | g0240 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00741 | hp1 | a0015 | c0036 | t0008 | g0019 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01069 | hp1 | a0009 | c0014 | t0001 | g0378 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01069 | hp2 | a0010 | c0017 | t0002 | g0160 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01070 | hp1 | a0009 | c0014 | t0001 | g0377 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01070 | hp2 | a0002 | c0001 | t0003 | g0257 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01071 | hp1 | a0009 | c0014 | t0001 | g0379 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01071 | hp2 | a0010 | c0017 | t0002 | g0159 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01074 | hp1 | a0002 | c0001 | t0003 | g0231 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01081 | hp2 | a0002 | c0001 | t0065 | g0239 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01099 | hp1 | a0002 | c0001 | t0003 | g0221 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0121 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01106 | hp2 | a0016 | c0023 | t0001 | g0319 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01109 | hp1 | a0002 | c0001 | t0003 | g0272 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01109 | hp2 | a0002 | c0001 | t0003 | g0273 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01169 | hp1 | a0001 | c0003 | t0055 | g0156 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01175 | hp1 | a0007 | c0012 | t0007 | g0291 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01175 | hp2 | a0001 | c0003 | t0037 | g0096 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01192 | hp2 | a0002 | c0001 | t0026 | g0015 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01243 | hp1 | a0017 | c0034 | t0063 | g0201 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0130 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01256 | hp1 | a0001 | c0016 | t0002 | g0100 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0314 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01258 | hp2 | a0001 | c0016 | t0002 | g0103 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01261 | hp1 | a0001 | c0003 | t0034 | g0148 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0344 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01358 | hp1 | a0001 | c0002 | t0013 | g0173 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01358 | hp2 | a0001 | c0004 | t0006 | g0059 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01433 | hp1 | a0002 | c0001 | t0003 | g0214 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0364 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01496 | hp1 | a0002 | c0001 | t0003 | g0254 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0104 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01515 | hp2 | a0002 | c0001 | t0003 | g0256 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0375 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0099 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01517 | hp1 | a0002 | c0001 | t0003 | g0255 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0101 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01884 | hp1 | a0002 | c0001 | t0066 | g0210 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01884 | hp2 | a0001 | c0003 | t0024 | g0268 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01891 | hp1 | a0001 | c0002 | t0025 | g0194 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01891 | hp2 | a0005 | c0010 | t0018 | g0247 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01934 | hp1 | a0001 | c0003 | t0035 | g0133 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01943 | hp1 | a0002 | c0001 | t0008 | g0033 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0315 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01975 | hp1 | a0002 | c0001 | t0008 | g0035 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0355 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01993 | hp1 | a0018 | c0028 | t0002 | g0123 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0358 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02004 | hp1 | a0002 | c0001 | t0008 | g0034 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0137 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02040 | hp1 | a0006 | c0011 | t0014 | g0093 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02040 | hp2 | a0002 | c0001 | t0004 | g0036 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02056 | hp1 | a0019 | c0033 | t0003 | g0202 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02056 | hp2 | a0001 | c0004 | t0005 | g0078 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02071 | hp1 | a0001 | c0004 | t0006 | g0054 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02074 | hp1 | a0002 | c0001 | t0069 | g0192 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02080 | hp2 | a0002 | c0001 | t0003 | g0196 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02083 | hp1 | a0020 | c0032 | t0062 | g0226 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02083 | hp2 | a0002 | c0001 | t0003 | g0224 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0142 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02132 | hp2 | a0001 | c0004 | t0006 | g0075 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02135 | hp2 | a0001 | c0003 | t0002 | g0143 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02145 | hp1 | a0003 | c0005 | t0007 | g0278 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02145 | hp2 | a0002 | c0001 | t0004 | g0046 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02148 | hp1 | a0002 | c0001 | t0008 | g0038 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02155 | hp1 | a0001 | c0002 | t0032 | g0172 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02155 | hp2 | a0001 | c0004 | t0005 | g0082 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02165 | hp1 | a0001 | c0003 | t0033 | g0113 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02165 | hp2 | a0001 | c0004 | t0005 | g0052 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02257 | hp1 | a0002 | c0001 | t0004 | g0017 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02257 | hp2 | a0003 | c0005 | t0007 | g0288 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02258 | hp1 | a0003 | c0005 | t0016 | g0181 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02258 | hp2 | a0001 | c0003 | t0054 | g0259 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02273 | hp1 | a0002 | c0001 | t0008 | g0009 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02280 | hp1 | a0021 | c0029 | t0030 | g0260 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02280 | hp2 | a0002 | c0001 | t0004 | g0023 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0361 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02293 | hp2 | a0002 | c0001 | t0008 | g0018 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02300 | hp1 | a0002 | c0001 | t0003 | g0227 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0144 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02451 | hp1 | a0002 | c0001 | t0004 | g0010 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02451 | hp2 | a0011 | c0015 | t0029 | g0004 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02523 | hp1 | a0001 | c0003 | t0002 | g0120 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02572 | hp1 | a0002 | c0001 | t0010 | g0212 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02572 | hp2 | a0022 | c0027 | t0016 | g0282 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02602 | hp1 | a0002 | c0001 | t0020 | g0031 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02602 | hp2 | a0001 | c0003 | t0028 | g0141 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02615 | hp1 | a0003 | c0005 | t0007 | g0296 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02615 | hp2 | a0002 | c0001 | t0004 | g0011 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02630 | hp1 | a0002 | c0001 | t0004 | g0048 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02630 | hp2 | a0001 | c0022 | t0025 | g0193 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02647 | hp1 | a0001 | c0007 | t0023 | g0271 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02647 | hp2 | a0003 | c0005 | t0007 | g0292 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02683 | hp1 | a0001 | c0002 | t0013 | g0175 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02683 | hp2 | a0002 | c0001 | t0012 | g0044 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02735 | hp1 | a0001 | c0004 | t0006 | g0077 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02735 | hp2 | a0002 | c0001 | t0017 | g0218 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02809 | hp1 | a0001 | c0007 | t0023 | g0263 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02809 | hp2 | a0002 | c0001 | t0004 | g0047 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02818 | hp1 | a0002 | c0001 | t0010 | g0232 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02818 | hp2 | a0005 | c0018 | t0031 | g0248 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02886 | hp1 | a0001 | c0002 | t0025 | g0195 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02886 | hp2 | a0011 | c0015 | t0029 | g0005 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02895 | hp1 | a0002 | c0001 | t0010 | g0235 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02895 | hp2 | a0003 | c0005 | t0016 | g0180 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02896 | hp1 | a0002 | c0001 | t0010 | g0208 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02896 | hp2 | a0001 | c0002 | t0046 | g0186 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02897 | hp1 | a0002 | c0001 | t0010 | g0234 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02897 | hp2 | a0003 | c0005 | t0016 | g0182 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02965 | hp1 | a0003 | c0019 | t0068 | g0287 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02965 | hp2 | a0001 | c0007 | t0022 | g0275 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03041 | hp1 | a0002 | c0001 | t0004 | g0022 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03041 | hp2 | a0001 | c0007 | t0022 | g0264 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03098 | hp1 | a0003 | c0005 | t0007 | g0286 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03098 | hp2 | a0001 | c0007 | t0023 | g0270 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03130 | hp1 | a0003 | c0005 | t0007 | g0284 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03130 | hp2 | a0002 | c0001 | t0010 | g0209 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03139 | hp1 | a0002 | c0001 | t0019 | g0006 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03139 | hp2 | a0001 | c0002 | t0048 | g0185 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03195 | hp1 | a0003 | c0005 | t0007 | g0279 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03195 | hp2 | a0005 | c0010 | t0018 | g0246 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03209 | hp1 | a0002 | c0001 | t0004 | g0026 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03209 | hp2 | a0002 | c0001 | t0003 | g0277 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03225 | hp1 | a0002 | c0001 | t0026 | g0043 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03225 | hp2 | a0003 | c0005 | t0007 | g0293 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03239 | hp1 | a0002 | c0001 | t0067 | g0211 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0138 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03453 | hp1 | a0002 | c0001 | t0026 | g0042 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03453 | hp2 | a0002 | c0001 | t0039 | g0025 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03486 | hp1 | a0001 | c0003 | t0058 | g0261 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03486 | hp2 | a0003 | c0005 | t0007 | g0280 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03491 | hp1 | a0001 | c0009 | t0015 | g0250 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03491 | hp2 | a0002 | c0001 | t0003 | g0188 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03492 | hp1 | a0002 | c0001 | t0003 | g0189 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03492 | hp2 | a0001 | c0004 | t0005 | g0065 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03516 | hp1 | a0002 | c0001 | t0004 | g0021 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03516 | hp2 | a0002 | c0001 | t0004 | g0020 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03540 | hp1 | a0002 | c0001 | t0004 | g0024 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03540 | hp2 | a0007 | c0012 | t0007 | g0294 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03579 | hp1 | a0002 | c0001 | t0019 | g0007 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03579 | hp2 | a0001 | c0003 | t0057 | g0262 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03654 | hp1 | a0005 | c0010 | t0018 | g0184 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0107 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03669 | hp1 | a0002 | c0001 | t0003 | g0241 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03669 | hp2 | a0001 | c0009 | t0015 | g0252 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03688 | hp1 | a0002 | c0001 | t0003 | g0190 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0304 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03704 | hp1 | a0001 | c0009 | t0015 | g0251 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03704 | hp2 | a0002 | c0001 | t0017 | g0229 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0132 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03710 | hp2 | a0001 | c0009 | t0015 | g0253 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03831 | hp1 | a0002 | c0001 | t0003 | g0187 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03831 | hp2 | a0001 | c0003 | t0002 | g0111 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03834 | hp1 | a0002 | c0001 | t0017 | g0230 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0356 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03942 | hp1 | a0001 | c0002 | t0045 | g0302 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03942 | hp2 | a0001 | c0004 | t0006 | g0071 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0102 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04115 | hp2 | a0002 | c0001 | t0020 | g0029 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0139 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04204 | hp2 | a0001 | c0004 | t0005 | g0085 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0321 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04228 | hp2 | a0002 | c0001 | t0017 | g0199 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18522 | hp1 | a0002 | c0001 | t0070 | g0003 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18522 | hp2 | a0001 | c0007 | t0022 | g0274 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18906 | hp1 | a0001 | c0003 | t0024 | g0266 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18906 | hp2 | a0002 | c0001 | t0004 | g0014 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18940 | hp2 | a0001 | c0003 | t0011 | g0150 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18942 | hp1 | a0002 | c0001 | t0061 | g0220 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18943 | hp1 | a0002 | c0001 | t0064 | g0213 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18945 | hp1 | a0001 | c0003 | t0002 | g0146 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18945 | hp2 | a0001 | c0004 | t0006 | g0074 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18946 | hp2 | a0002 | c0013 | t0003 | g0242 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18947 | hp1 | a0002 | c0001 | t0003 | g0233 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18947 | hp2 | a0001 | c0003 | t0002 | g0106 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18948 | hp2 | a0001 | c0004 | t0005 | g0064 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18950 | hp1 | a0001 | c0004 | t0005 | g0083 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18950 | hp2 | a0023 | c0020 | t0003 | g0236 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18951 | hp2 | a0002 | c0001 | t0003 | g0205 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18952 | hp2 | a0002 | c0001 | t0003 | g0222 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18953 | hp1 | a0001 | c0003 | t0036 | g0125 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18953 | hp2 | a0001 | c0004 | t0005 | g0086 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18957 | hp1 | a0002 | c0001 | t0004 | g0037 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18957 | hp2 | a0001 | c0003 | t0027 | g0115 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18960 | hp1 | a0001 | c0003 | t0011 | g0135 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18960 | hp2 | a0002 | c0001 | t0003 | g0219 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18961 | hp1 | a0002 | c0001 | t0003 | g0217 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18961 | hp2 | a0001 | c0003 | t0027 | g0114 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18962 | hp1 | a0002 | c0001 | t0004 | g0040 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18962 | hp2 | a0004 | c0006 | t0009 | g0161 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18963 | hp1 | a0001 | c0002 | t0051 | g0363 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18963 | hp2 | a0002 | c0001 | t0003 | g0225 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18966 | hp2 | a0008 | c0008 | t0001 | g0348 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18968 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18968 | hp2 | a0002 | c0001 | t0012 | g0066 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18970 | hp1 | a0001 | c0002 | t0047 | g0357 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18970 | hp2 | a0002 | c0001 | t0012 | g0068 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18971 | hp1 | a0001 | c0004 | t0006 | g0055 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18972 | hp1 | a0006 | c0011 | t0014 | g0177 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18972 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18973 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0228 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18977 | hp2 | a0001 | c0003 | t0002 | g0145 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18978 | hp1 | a0002 | c0001 | t0004 | g0039 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18978 | hp2 | a0001 | c0004 | t0005 | g0063 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18980 | hp2 | a0024 | c0035 | t0003 | g0258 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18981 | hp1 | a0008 | c0008 | t0001 | g0341 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18981 | hp2 | a0001 | c0004 | t0005 | g0080 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18983 | hp1 | a0004 | c0006 | t0009 | g0165 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18984 | hp1 | a0008 | c0008 | t0001 | g0299 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18984 | hp2 | a0001 | c0003 | t0011 | g0116 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18986 | hp1 | a0002 | c0001 | t0003 | g0179 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18986 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18987 | hp1 | a0001 | c0004 | t0005 | g0081 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18987 | hp2 | a0001 | c0002 | t0050 | g0327 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18989 | hp1 | a0001 | c0004 | t0006 | g0057 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18990 | hp1 | a0004 | c0006 | t0009 | g0164 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18990 | hp2 | a0001 | c0002 | t0021 | g0324 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18991 | hp1 | a0001 | c0004 | t0005 | g0062 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18991 | hp2 | a0001 | c0002 | t0013 | g0095 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18992 | hp2 | a0001 | c0004 | t0006 | g0067 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0151 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18993 | hp2 | a0002 | c0001 | t0003 | g0237 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18994 | hp1 | a0002 | c0001 | t0003 | g0244 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18994 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0105 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18998 | hp2 | a0001 | c0004 | t0006 | g0073 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19000 | hp2 | a0001 | c0003 | t0056 | g0309 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19001 | hp2 | a0001 | c0004 | t0006 | g0056 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19003 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19005 | hp1 | a0002 | c0013 | t0003 | g0198 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19005 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19007 | hp2 | a0001 | c0004 | t0006 | g0058 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19009 | hp1 | a0001 | c0004 | t0005 | g0094 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19010 | hp1 | a0001 | c0003 | t0011 | g0152 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19010 | hp2 | a0002 | c0001 | t0004 | g0041 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19011 | hp1 | a0001 | c0004 | t0005 | g0090 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19011 | hp2 | a0002 | c0001 | t0003 | g0203 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19030 | hp1 | a0007 | c0012 | t0007 | g0290 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19030 | hp2 | a0002 | c0001 | t0004 | g0012 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19043 | hp1 | a0001 | c0003 | t0024 | g0267 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19043 | hp2 | a0002 | c0001 | t0019 | g0008 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19056 | hp1 | a0002 | c0001 | t0003 | g0207 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19060 | hp1 | a0002 | c0001 | t0003 | g0223 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19060 | hp2 | a0025 | c0025 | t0001 | g0360 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19063 | hp1 | a0001 | c0003 | t0011 | g0155 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19063 | hp2 | a0002 | c0001 | t0003 | g0216 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19064 | hp1 | a0004 | c0006 | t0009 | g0170 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19065 | hp2 | a0001 | c0003 | t0002 | g0128 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19066 | hp1 | a0008 | c0008 | t0001 | g0338 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19066 | hp2 | a0026 | c0031 | t0002 | g0167 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19068 | hp1 | a0001 | c0004 | t0043 | g0061 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19070 | hp1 | a0004 | c0006 | t0009 | g0163 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19074 | hp2 | a0001 | c0002 | t0013 | g0091 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19076 | hp2 | a0001 | c0004 | t0006 | g0060 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19078 | hp2 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19079 | hp2 | a0001 | c0004 | t0005 | g0087 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19081 | hp1 | a0002 | c0013 | t0003 | g0197 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19081 | hp2 | a0027 | c0030 | t0006 | g0072 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19084 | hp1 | a0028 | c0037 | t0021 | g0334 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19084 | hp2 | a0002 | c0001 | t0003 | g0243 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19085 | hp1 | a0002 | c0001 | t0003 | g0204 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19085 | hp2 | a0004 | c0006 | t0009 | g0169 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19086 | hp1 | a0002 | c0001 | t0003 | g0200 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19086 | hp2 | a0001 | c0004 | t0044 | g0088 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19088 | hp2 | a0002 | c0001 | t0012 | g0069 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19090 | hp2 | a0004 | c0006 | t0009 | g0162 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19091 | hp1 | a0001 | c0004 | t0006 | g0070 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19091 | hp2 | a0001 | c0002 | t0021 | g0350 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19240 | hp1 | a0002 | c0001 | t0004 | g0028 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19240 | hp2 | a0003 | c0005 | t0007 | g0295 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20129 | hp1 | a0007 | c0012 | t0007 | g0289 | AFR | ASW | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20129 | hp2 | a0001 | c0038 | t0030 | g0265 | AFR | ASW | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20752 | hp1 | a0002 | c0001 | t0020 | g0030 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0097 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20805 | hp1 | a0002 | c0001 | t0060 | g0373 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20805 | hp2 | a0005 | c0010 | t0018 | g0183 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20905 | hp1 | a0002 | c0001 | t0008 | g0032 | SAS | GIH | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0367 | SAS | GIH | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01123 | hp2 | a0001 | c0003 | t0028 | g0140 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02559 | hp1 | a0001 | c0004 | t0041 | g0053 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02559 | hp2 | a0002 | c0001 | t0003 | g0276 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03471 | hp1 | a0002 | c0001 | t0004 | g0013 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03471 | hp2 | a0002 | c0001 | t0004 | g0016 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG06807 | hp1 | a0001 | c0003 | t0059 | g0269 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG06807 | hp2 | a0003 | c0005 | t0007 | g0281 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18955 | hp1 | a0001 | c0004 | t0005 | g0089 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18955 | hp2 | a0002 | c0001 | t0003 | g0191 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20300 | hp1 | a0002 | c0001 | t0038 | g0027 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20300 | hp2 | a0005 | c0018 | t0031 | g0249 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
homoSapiens | chm13v2 | a0001 | c0003 | t0042 | g0098 | REF | REF | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
homoSapiens | grch38p0 | a0002 | c0001 | t0003 | g0283 | REF | REF | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151420263 | G | A | 1 | a0011 | 2 | HG02451.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.577G>A | p.Val193Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/36 | 719/14662 | 577/7419 | 193/2472 | chr2 | 151420263 | |||
chr2:151435557 | A | G | 1 | a0007 | 4 | HG01175.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
missense_variant | MODERATE | c.1172A>G | p.Asn391Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/36 | 1314/14662 | 1172/7419 | 391/2472 | chr2 | 151435557 | |||
chr2:151436856 | A | G | 1 | a0028 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1225A>G | p.Thr409Ala | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/36 | 1367/14662 | 1225/7419 | 409/2472 | chr2 | 151436856 | |||
chr2:151441977 | A | G | 1 | a0015 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1720A>G | p.Met574Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/36 | 1862/14662 | 1720/7419 | 574/2472 | chr2 | 151441977 | |||
chr2:151443629 | G | A | 1 | a0023 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.1906G>A | p.Ala636Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/36 | 2048/14662 | 1906/7419 | 636/2472 | chr2 | 151443629 | |||
chr2:151455056 | G | A | 21 | a0001 a0003 a0004 others(18): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
missense_variant | MODERATE | c.2506G>A | p.Gly836Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2648/14662 | 2506/7419 | 836/2472 | chr2 | 151455056 | |||
chr2:151455098 | A | G | 1 | a0005 | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
missense_variant | MODERATE | c.2548A>G | p.Met850Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2690/14662 | 2548/7419 | 850/2472 | chr2 | 151455098 | |||
chr2:151455110 | A | T | 1 | a0026 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2560A>T | p.Ile854Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2702/14662 | 2560/7419 | 854/2472 | chr2 | 151455110 | |||
chr2:151458885 | A | T | 1 | a0027 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.2930A>T | p.Glu977Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/36 | 3072/14662 | 2930/7419 | 977/2472 | chr2 | 151458885 | |||
chr2:151462304 | A | G | 1 | a0021 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.3290A>G | p.Tyr1097Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/36 | 3432/14662 | 3290/7419 | 1097/2472 | chr2 | 151462304 | |||
chr2:151462944 | G | A | 1 | a0008 | 4 | NA18966.hp2 NA18981.hp1 NA18984.hp1 others(1): Show |
missense_variant | MODERATE | c.3424G>A | p.Ala1142Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 3566/14662 | 3424/7419 | 1142/2472 | chr2 | 151462944 | |||
chr2:151463429 | G | C | 1 | a0014 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.3909G>C | p.Lys1303Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4051/14662 | 3909/7419 | 1303/2472 | chr2 | 151463429 | |||
chr2:151463604 | G | A | 22 | a0001 a0003 a0004 others(19): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
missense_variant | MODERATE | c.4084G>A | p.Val1362Met | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4226/14662 | 4084/7419 | 1362/2472 | chr2 | 151463604 | |||
chr2:151463803 | C | T | 1 | a0025 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.4283C>T | p.Thr1428Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4425/14662 | 4283/7419 | 1428/2472 | chr2 | 151463803 | |||
chr2:151464039 | G | A | 1 | a0013 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.4519G>A | p.Asp1507Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4661/14662 | 4519/7419 | 1507/2472 | chr2 | 151464039 | |||
chr2:151464056 | G | T | 1 | a0012 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.4536G>T | p.Lys1512Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4678/14662 | 4536/7419 | 1512/2472 | chr2 | 151464056 | |||
chr2:151464250 | A | G | 1 | a0010 | 2 | HG01069.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.4730A>G | p.Asn1577Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4872/14662 | 4730/7419 | 1577/2472 | chr2 | 151464250 | |||
chr2:151464378 | G | A | 1 | a0004 | 7 | NA18962.hp2 NA18983.hp1 NA18990.hp1 others(4): Show |
missense_variant | MODERATE | c.4858G>A | p.Glu1620Lys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5000/14662 | 4858/7419 | 1620/2472 | chr2 | 151464378 | |||
chr2:151464576 | C | G | 1 | a0006 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
missense_variant | MODERATE | c.5056C>G | p.Arg1686Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5198/14662 | 5056/7419 | 1686/2472 | chr2 | 151464576 | |||
chr2:151464811 | A | C | 1 | a0024 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.5291A>C | p.Lys1764Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5433/14662 | 5291/7419 | 1764/2472 | chr2 | 151464811 | |||
chr2:151465002 | C | T | 1 | a0016 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.5482C>T | p.Pro1828Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5624/14662 | 5482/7419 | 1828/2472 | chr2 | 151465002 | |||
chr2:151465104 | G | A | 3 | a0003 a0007 a0022 |
21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
missense_variant | MODERATE | c.5584G>A | p.Val1862Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5726/14662 | 5584/7419 | 1862/2472 | chr2 | 151465104 | |||
chr2:151465150 | T | C | 1 | a0022 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.5630T>C | p.Leu1877Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5772/14662 | 5630/7419 | 1877/2472 | chr2 | 151465150 | |||
chr2:151465581 | A | T | 23 | a0001 a0003 a0004 others(20): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
missense_variant | MODERATE | c.6061A>T | p.Asn2021Tyr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6203/14662 | 6061/7419 | 2021/2472 | chr2 | 151465581 | |||
chr2:151465599 | G | A | 1 | a0018 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.6079G>A | p.Gly2027Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6221/14662 | 6079/7419 | 2027/2472 | chr2 | 151465599 | |||
chr2:151473973 | C | T | 1 | a0009 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.7105C>T | p.Arg2369Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/36 | 7247/14662 | 7105/7419 | 2369/2472 | chr2 | 151473973 | |||
chr2:151474048 | C | T | 1 | a0019 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.7180C>T | p.Pro2394Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/36 | 7322/14662 | 7180/7419 | 2394/2472 | chr2 | 151474048 | |||
chr2:151474904 | C | G | 22 | a0001 a0003 a0004 others(19): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
missense_variant | MODERATE | c.7252C>G | p.Leu2418Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 7394/14662 | 7252/7419 | 2418/2472 | chr2 | 151474904 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151420361 | G | A | 1 | a0003c0019 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.675G>A | p.Thr225Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/36 | 817/14662 | 675/7419 | 225/2472 | chr2 | 151420361 | |||
chr2:151435483 | A | G | 1 | a0001c0038 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1098A>G | p.Gln366Gln | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/36 | 1240/14662 | 1098/7419 | 366/2472 | chr2 | 151435483 | |||
chr2:151436855 | A | C | 1 | a0009c0014 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.1224A>C | p.Gly408Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/36 | 1366/14662 | 1224/7419 | 408/2472 | chr2 | 151436855 | |||
chr2:151440127 | G | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1647G>T | p.Leu549Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/36 | 1789/14662 | 1647/7419 | 549/2472 | chr2 | 151440127 | |||
chr2:151443309 | A | G | 1 | a0011c0015 | 2 | HG02451.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.1785A>G | p.Glu595Glu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 17/36 | 1927/14662 | 1785/7419 | 595/2472 | chr2 | 151443309 | |||
chr2:151446428 | C | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.2097C>T | p.Ala699Ala | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/36 | 2239/14662 | 2097/7419 | 699/2472 | chr2 | 151446428 | |||
chr2:151457871 | G | A | 12 | a0001c0002 a0001c0009 a0001c0022 others(9): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
synonymous_variant | LOW | c.2763G>A | p.Leu921Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/36 | 2905/14662 | 2763/7419 | 921/2472 | chr2 | 151457871 | |||
chr2:151461155 | G | A | 2 | a0001c0004 a0027c0030 |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
synonymous_variant | LOW | c.3093G>A | p.Ser1031Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/36 | 3235/14662 | 3093/7419 | 1031/2472 | chr2 | 151461155 | |||
chr2:151463450 | G | A | 1 | a0021c0029 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.3930G>A | p.Pro1310Pro | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4072/14662 | 3930/7419 | 1310/2472 | chr2 | 151463450 | |||
chr2:151463987 | T | C | 1 | a0001c0007 | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.4467T>C | p.Thr1489Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4609/14662 | 4467/7419 | 1489/2472 | chr2 | 151463987 | |||
chr2:151464017 | T | G | 1 | a0005c0018 | 2 | HG02818.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.4497T>G | p.Thr1499Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4639/14662 | 4497/7419 | 1499/2472 | chr2 | 151464017 | |||
chr2:151464596 | T | C | 1 | a0001c0009 | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.5076T>C | p.Cys1692Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5218/14662 | 5076/7419 | 1692/2472 | chr2 | 151464596 | |||
chr2:151464758 | C | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
synonymous_variant | LOW | c.5238C>T | p.Leu1746Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5380/14662 | 5238/7419 | 1746/2472 | chr2 | 151464758 | |||
chr2:151465601 | C | T | 1 | a0002c0013 | 3 | NA18946.hp2 NA19005.hp1 NA19081.hp1 |
synonymous_variant | LOW | c.6081C>T | p.Gly2027Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6223/14662 | 6081/7419 | 2027/2472 | chr2 | 151465601 | |||
chr2:151469756 | T | C | 1 | a0001c0016 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.6987T>C | p.Thr2329Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/36 | 7129/14662 | 6987/7419 | 2329/2472 | chr2 | 151469756 | |||
chr2:151469798 | T | C | 1 | a0001c0022 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.7029T>C | p.Thr2343Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/36 | 7171/14662 | 7029/7419 | 2343/2472 | chr2 | 151469798 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151409951 | G | T | 2 | a0002c0001t0026 a0002c0001t0070 |
4 | HG01192.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 473 | chr2 | 151409951 | ||||||
chr2:151409959 | T | C | 35 | a0001c0002t0013 a0001c0002t0032 a0001c0003t0002 others(32): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-85T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 465 | chr2 | 151409959 | ||||||
chr2:151409963 | A | G | 1 | a0002c0001t0070 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 461 | chr2 | 151409963 | ||||||
chr2:151475231 | T | G | 18 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(15): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 160 | chr2 | 151475231 | ||||||
chr2:151475255 | C | CTT | 5 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0043 others(2): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*194dupTT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 195 | INFO_REALIGN_3_PRIME | chr2 | 151475255 | |||||
chr2:151475313 | A | G | 1 | a0002c0001t0069 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 242 | chr2 | 151475313 | ||||||
chr2:151475481 | TGTTG | T | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*414_*417delGGTT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 414 | INFO_REALIGN_3_PRIME | chr2 | 151475481 | |||||
chr2:151475485 | G | T | 59 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(56): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 414 | chr2 | 151475485 | ||||||
chr2:151475652 | T | C | 1 | a0001c0002t0045 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 581 | chr2 | 151475652 | ||||||
chr2:151475726 | CTTA | C | 1 | a0001c0009t0015 | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*659delTAT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 657 | INFO_REALIGN_3_PRIME | chr2 | 151475726 | |||||
chr2:151475811 | C | A | 1 | a0002c0001t0053 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*740C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 740 | chr2 | 151475811 | ||||||
chr2:151475910 | C | T | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*839C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 839 | chr2 | 151475910 | ||||||
chr2:151475913 | C | T | 1 | a0003c0019t0068 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 842 | chr2 | 151475913 | ||||||
chr2:151476308 | G | A | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1237 | chr2 | 151476308 | ||||||
chr2:151476376 | A | G | 1 | a0013c0026t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1305A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1305 | chr2 | 151476376 | ||||||
chr2:151476419 | A | T | 1 | a0001c0002t0052 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1348 | chr2 | 151476419 | ||||||
chr2:151476433 | T | C | 1 | a0001c0003t0033 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1362 | chr2 | 151476433 | ||||||
chr2:151476583 | C | A | 2 | a0001c0007t0022 a0001c0007t0023 |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1512C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1512 | chr2 | 151476583 | ||||||
chr2:151476604 | C | G | 23 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(20): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1533C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1533 | chr2 | 151476604 | ||||||
chr2:151476668 | T | G | 1 | a0001c0003t0027 | 2 | NA18957.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1597 | chr2 | 151476668 | ||||||
chr2:151476790 | C | A | 31 | a0001c0003t0002 a0001c0003t0011 a0001c0003t0024 others(28): Show |
118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1719 | chr2 | 151476790 | ||||||
chr2:151476845 | A | G | 1 | a0001c0002t0032 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1774 | chr2 | 151476845 | ||||||
chr2:151476930 | G | A | 1 | a0001c0003t0054 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1859 | chr2 | 151476930 | ||||||
chr2:151476954 | T | TG | 2 | a0002c0001t0012 a0002c0001t0060 |
6 | HG00323.hp1 HG02683.hp2 NA18968.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1883_*1884insG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1884 | chr2 | 151476954 | ||||||
chr2:151477074 | T | G | 1 | a0001c0004t0043 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2003T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2003 | chr2 | 151477074 | ||||||
chr2:151477098 | T | G | 1 | a0013c0026t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2027 | chr2 | 151477098 | ||||||
chr2:151477258 | A | G | 2 | a0002c0001t0017 a0002c0001t0067 |
5 | HG02735.hp2 HG03239.hp1 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2187A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2187 | chr2 | 151477258 | ||||||
chr2:151477259 | C | T | 31 | a0001c0003t0002 a0001c0003t0011 a0001c0003t0024 others(28): Show |
118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2188C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2188 | chr2 | 151477259 | ||||||
chr2:151477298 | G | A | 62 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(59): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2227 | chr2 | 151477298 | ||||||
chr2:151477335 | A | C | 1 | a0001c0002t0051 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2264A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2264 | chr2 | 151477335 | ||||||
chr2:151477404 | A | G | 1 | a0001c0003t0059 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2333A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2333 | chr2 | 151477404 | ||||||
chr2:151477411 | T | C | 1 | a0005c0018t0031 | 2 | HG02818.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2340T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2340 | chr2 | 151477411 | ||||||
chr2:151477471 | A | C | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2400A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2400 | chr2 | 151477471 | ||||||
chr2:151477513 | T | C | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2442T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2442 | chr2 | 151477513 | ||||||
chr2:151477563 | C | T | 1 | a0013c0026t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2492C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2492 | chr2 | 151477563 | ||||||
chr2:151477773 | G | A | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2702G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2702 | chr2 | 151477773 | ||||||
chr2:151477798 | C | A | 1 | a0002c0001t0069 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2727 | chr2 | 151477798 | ||||||
chr2:151477805 | G | A | 1 | a0002c0001t0067 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2734G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2734 | chr2 | 151477805 | ||||||
chr2:151477819 | C | T | 1 | a0011c0015t0029 | 2 | HG02451.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2748C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2748 | chr2 | 151477819 | ||||||
chr2:151477979 | C | A | 8 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(5): Show |
42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2908C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2908 | chr2 | 151477979 | ||||||
chr2:151478024 | T | G | 1 | a0002c0001t0038 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2953 | chr2 | 151478024 | ||||||
chr2:151478066 | A | G | 26 | a0001c0003t0002 a0001c0003t0011 a0001c0003t0027 others(23): Show |
122 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2995A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2995 | chr2 | 151478066 | ||||||
chr2:151478190 | C | T | 1 | a0001c0003t0028 | 2 | HG01123.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3119C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3119 | chr2 | 151478190 | ||||||
chr2:151478355 | G | A | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3284G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3284 | chr2 | 151478355 | ||||||
chr2:151478450 | C | T | 1 | a0001c0003t0037 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3379C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3379 | chr2 | 151478450 | ||||||
chr2:151478452 | C | T | 1 | a0001c0003t0058 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3381 | chr2 | 151478452 | ||||||
chr2:151478462 | AG | A | 3 | a0002c0001t0010 a0002c0001t0065 a0002c0001t0066 |
8 | HG01081.hp2 HG01884.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3392delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3392 | chr2 | 151478462 | ||||||
chr2:151478474 | G | A | 23 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(20): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3403G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3403 | chr2 | 151478474 | ||||||
chr2:151478475 | CA | C | 3 | a0001c0002t0050 a0002c0001t0064 a0006c0011t0014 |
6 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3419delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3419 | INFO_REALIGN_3_PRIME | chr2 | 151478475 | |||||
chr2:151478516 | T | C | 1 | a0002c0001t0010 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3445T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3445 | chr2 | 151478516 | ||||||
chr2:151478533 | A | C | 1 | a0001c0004t0041 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3462A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3462 | chr2 | 151478533 | ||||||
chr2:151478547 | ATAGT | A | 2 | a0001c0003t0011 a0001c0003t0027 |
7 | NA18940.hp2 NA18957.hp2 NA18960.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3479_*3482delGTTA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3479 | INFO_REALIGN_3_PRIME | chr2 | 151478547 | |||||
chr2:151478620 | T | G | 1 | a0001c0002t0046 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3549T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3549 | chr2 | 151478620 | ||||||
chr2:151478648 | A | G | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3577A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3577 | chr2 | 151478648 | ||||||
chr2:151478676 | T | TA | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3608dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3609 | INFO_REALIGN_3_PRIME | chr2 | 151478676 | |||||
chr2:151478835 | G | A | 1 | a0001c0003t0034 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3764G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3764 | chr2 | 151478835 | ||||||
chr2:151478866 | T | C | 23 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(20): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3795T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3795 | chr2 | 151478866 | ||||||
chr2:151478920 | TG | T | 62 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(59): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*3851delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3851 | INFO_REALIGN_3_PRIME | chr2 | 151478920 | |||||
chr2:151479196 | A | G | 2 | a0001c0007t0022 a0001c0007t0023 |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4125 | chr2 | 151479196 | ||||||
chr2:151479306 | G | A | 1 | a0002c0001t0061 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4235G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4235 | chr2 | 151479306 | ||||||
chr2:151479512 | A | G | 2 | a0005c0010t0018 a0005c0018t0031 |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4441A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4441 | chr2 | 151479512 | ||||||
chr2:151479523 | C | T | 7 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(4): Show |
38 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4452C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4452 | chr2 | 151479523 | ||||||
chr2:151479575 | A | G | 1 | a0001c0002t0048 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4504A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4504 | chr2 | 151479575 | ||||||
chr2:151479599 | T | C | 1 | a0013c0026t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4528T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4528 | chr2 | 151479599 | ||||||
chr2:151479665 | G | A | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4594G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4594 | chr2 | 151479665 | ||||||
chr2:151479734 | G | A | 1 | a0002c0001t0065 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4663G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4663 | chr2 | 151479734 | ||||||
chr2:151479914 | A | G | 64 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(61): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*4843A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4843 | chr2 | 151479914 | ||||||
chr2:151479974 | A | G | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4903A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4903 | chr2 | 151479974 | ||||||
chr2:151479989 | T | C | 1 | a0001c0003t0035 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4918T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4918 | chr2 | 151479989 | ||||||
chr2:151480003 | A | G | 2 | a0001c0003t0024 a0001c0003t0059 |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4932A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4932 | chr2 | 151480003 | ||||||
chr2:151480214 | T | G | 1 | a0002c0001t0019 | 3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5143T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5143 | chr2 | 151480214 | ||||||
chr2:151480284 | C | A | 2 | a0001c0002t0021 a0028c0037t0021 |
3 | NA18990.hp2 NA19084.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5213C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5213 | chr2 | 151480284 | ||||||
chr2:151480336 | A | C | 2 | a0001c0003t0057 a0001c0003t0058 |
2 | HG03486.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5265A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5265 | chr2 | 151480336 | ||||||
chr2:151480415 | T | G | 1 | a0004c0006t0009 | 7 | NA18962.hp2 NA18983.hp1 NA18990.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5344T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5344 | chr2 | 151480415 | ||||||
chr2:151480491 | A | G | 1 | a0001c0007t0023 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5420A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5420 | chr2 | 151480491 | ||||||
chr2:151480515 | C | T | 1 | a0002c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5444C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5444 | chr2 | 151480515 | ||||||
chr2:151480764 | ATTTTT | A | 2 | a0002c0001t0008 a0015c0036t0008 |
8 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5695_*5699delTTTT others(1): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5695 | INFO_REALIGN_3_PRIME | chr2 | 151480764 | |||||
chr2:151480766 | T | G | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5695T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5695 | chr2 | 151480766 | ||||||
chr2:151480797 | A | C | 1 | a0002c0001t0020 | 3 | HG02602.hp1 HG04115.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5726A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5726 | chr2 | 151480797 | ||||||
chr2:151480861 | C | G | 1 | a0001c0004t0044 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5790C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5790 | chr2 | 151480861 | ||||||
chr2:151480885 | T | G | 1 | a0001c0003t0055 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5814T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5814 | chr2 | 151480885 | ||||||
chr2:151480950 | T | C | 3 | a0001c0004t0005 a0001c0004t0043 a0001c0004t0044 |
20 | HG00597.hp1 HG00673.hp1 HG02056.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5879T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5879 | chr2 | 151480950 | ||||||
chr2:151480969 | A | AAGG | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5900_*5901insGAG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5901 | INFO_REALIGN_3_PRIME | chr2 | 151480969 | |||||
chr2:151480972 | A | AAGG | 55 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(52): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*5903_*5905dupGGA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5906 | INFO_REALIGN_3_PRIME | chr2 | 151480972 | |||||
chr2:151480972 | A | G | 8 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(5): Show |
43 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5901A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5901 | chr2 | 151480972 | ||||||
chr2:151481041 | G | A | 2 | a0001c0002t0025 a0001c0022t0025 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5970G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5970 | chr2 | 151481041 | ||||||
chr2:151481122 | C | T | 2 | a0003c0005t0016 a0022c0027t0016 |
4 | HG02258.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6051C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6051 | chr2 | 151481122 | ||||||
chr2:151481272 | G | A | 5 | a0003c0005t0007 a0003c0005t0016 a0003c0019t0068 others(2): Show |
21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6201G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6201 | chr2 | 151481272 | ||||||
chr2:151481274 | G | A | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6203G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6203 | chr2 | 151481274 | ||||||
chr2:151481282 | G | A | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6211G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6211 | chr2 | 151481282 | ||||||
chr2:151481308 | G | A | 17 | a0001c0003t0002 a0001c0003t0011 a0001c0003t0027 others(14): Show |
81 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*6237G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6237 | chr2 | 151481308 | ||||||
chr2:151481556 | G | A | 1 | a0001c0002t0047 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6485G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6485 | chr2 | 151481556 | ||||||
chr2:151481723 | A | G | 1 | a0002c0001t0039 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6652A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6652 | chr2 | 151481723 | ||||||
chr2:151481889 | C | G | 1 | a0006c0011t0014 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6818C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6818 | chr2 | 151481889 | ||||||
chr2:151481893 | A | G | 1 | a0013c0026t0040 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6822A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6822 | chr2 | 151481893 | ||||||
chr2:151481903 | C | T | 6 | a0001c0004t0005 a0001c0004t0006 a0001c0004t0041 others(3): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6832C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6832 | chr2 | 151481903 | ||||||
chr2:151481926 | C | A | 1 | a0001c0003t0036 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6855C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6855 | chr2 | 151481926 | ||||||
chr2:151482024 | AG | A | 62 | a0001c0002t0001 a0001c0002t0013 a0001c0002t0021 others(59): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*6960delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6960 | INFO_REALIGN_3_PRIME | chr2 | 151482024 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151410217 | T | A | 175 | a0001c0002t0013g0091 a0001c0002t0013g0095 a0001c0002t0013g0173 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-11+184T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410217 | |||||||
chr2:151410226 | G | A | 1 | a0001c0002t0001g0178 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-10-188G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410226 | |||||||
chr2:151410228 | G | T | 2 | a0006c0011t0014g0176 a0006c0011t0014g0177 |
2 | HG00423.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-10-186G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410228 | |||||||
chr2:151410547 | G | A | 47 | a0001c0003t0002g0002 a0002c0001t0004g0010 a0002c0001t0004g0011 others(44): Show |
47 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.104+20G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410547 | |||||||
chr2:151410558 | T | G | 174 | a0001c0002t0013g0091 a0001c0002t0013g0095 a0001c0002t0013g0173 others(171): Show |
174 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.104+31T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410558 | |||||||
chr2:151410764 | T | C | 3 | a0003c0005t0016g0180 a0003c0005t0016g0181 a0003c0005t0016g0182 |
3 | HG02258.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.104+237T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410764 | |||||||
chr2:151410824 | A | G | 1 | a0002c0001t0004g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+297A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410824 | |||||||
chr2:151410845 | G | T | 88 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(85): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.104+318G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410845 | |||||||
chr2:151410865 | A | AGTT | 260 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(257): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.104+339_104+341dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr2 | 151410865 | ||||||
chr2:151410969 | T | G | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.105-291T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410969 | |||||||
chr2:151410998 | G | T | 1 | a0002c0001t0004g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.105-262G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410998 | |||||||
chr2:151411065 | C | T | 3 | a0009c0014t0001g0377 a0009c0014t0001g0378 a0009c0014t0001g0379 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.105-195C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411065 | |||||||
chr2:151411142 | G | T | 1 | a0001c0004t0005g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.105-118G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411142 | |||||||
chr2:151411158 | G | A | 356 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(353): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.105-102G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411158 | |||||||
chr2:151411202 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-58A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411202 | |||||||
chr2:151411207 | AT | A | 80 | a0001c0002t0013g0095 a0001c0003t0002g0002 a0001c0003t0002g0049 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.105-42delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr2 | 151411207 | ||||||
chr2:151411226 | A | G | 1 | a0001c0002t0001g0376 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.105-34A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411226 | |||||||
chr2:151411361 | G | GTTTTTCA others(17): Show |
1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.183+29_183+52dupCA others(22): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151411361 | ||||||
chr2:151411383 | G | GT | 82 | a0001c0002t0001g0375 a0001c0003t0002g0002 a0001c0003t0002g0049 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.183+56dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151411383 | ||||||
chr2:151411460 | A | G | 1 | a0001c0002t0001g0374 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.183+122A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411460 | |||||||
chr2:151411472 | G | A | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.183+134G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411472 | |||||||
chr2:151411632 | C | G | 4 | a0002c0001t0003g0254 a0002c0001t0003g0255 a0002c0001t0003g0256 others(1): Show |
4 | HG01070.hp2 HG01496.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+294C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411632 | |||||||
chr2:151411814 | C | G | 10 | a0001c0003t0002g0166 a0001c0003t0002g0168 a0004c0006t0009g0161 others(7): Show |
10 | NA18962.hp2 NA18973.hp1 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+476C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411814 | |||||||
chr2:151411827 | C | A | 2 | a0005c0010t0018g0183 a0005c0010t0018g0184 |
2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.183+489C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411827 | |||||||
chr2:151411938 | G | C | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+600G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411938 | |||||||
chr2:151411981 | C | G | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+643C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411981 | |||||||
chr2:151411996 | T | G | 1 | a0001c0002t0001g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+658T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411996 | |||||||
chr2:151412043 | T | C | 40 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(37): Show |
40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.183+705T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412043 | |||||||
chr2:151412050 | A | G | 45 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(42): Show |
45 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.183+712A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412050 | |||||||
chr2:151412063 | T | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+725T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412063 | |||||||
chr2:151412200 | C | A | 2 | a0001c0003t0057g0262 a0001c0003t0058g0261 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.183+862C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412200 | |||||||
chr2:151412224 | T | C | 1 | a0001c0002t0001g0298 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.183+886T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412224 | |||||||
chr2:151412260 | G | GTTTC | 356 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(353): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.183+925_183+926ins others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412260 | ||||||
chr2:151412291 | C | T | 261 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.183+953C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412291 | |||||||
chr2:151412309 | GT | G | 91 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(88): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.183+974delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412309 | ||||||
chr2:151412321 | TATG | T | 79 | a0001c0003t0002g0049 a0001c0003t0002g0050 a0001c0003t0002g0097 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.183+985_183+987del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412321 | ||||||
chr2:151412339 | C | T | 1 | a0006c0011t0014g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.183+1001C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412339 | |||||||
chr2:151412343 | T | C | 40 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(37): Show |
40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.183+1005T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412343 | |||||||
chr2:151412389 | T | C | 4 | a0002c0001t0003g0187 a0002c0001t0003g0188 a0002c0001t0003g0189 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1051T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412389 | |||||||
chr2:151412498 | G | A | 10 | a0001c0003t0002g0166 a0001c0003t0002g0168 a0004c0006t0009g0161 others(7): Show |
10 | NA18962.hp2 NA18973.hp1 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+1160G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412498 | |||||||
chr2:151412599 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1261C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412599 | |||||||
chr2:151412729 | C | T | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+1391C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412729 | |||||||
chr2:151412744 | G | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1406G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412744 | |||||||
chr2:151412823 | T | G | 1 | a0001c0003t0002g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.183+1485T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412823 | |||||||
chr2:151413041 | A | G | 2 | a0002c0001t0003g0276 a0002c0001t0003g0277 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183+1703A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413041 | |||||||
chr2:151413049 | CT | C | 44 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(41): Show |
44 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.183+1724delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151413049 | ||||||
chr2:151413184 | G | A | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1639G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413184 | |||||||
chr2:151413276 | G | A | 1 | a0002c0001t0069g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184-1547G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413276 | |||||||
chr2:151413318 | A | G | 4 | a0001c0003t0002g0002 a0002c0001t0012g0044 a0002c0001t0012g0045 others(1): Show |
4 | HG00323.hp1 HG02683.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1505A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413318 | |||||||
chr2:151413406 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1417T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413406 | |||||||
chr2:151413488 | A | G | 2 | a0010c0017t0002g0159 a0010c0017t0002g0160 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.184-1335A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413488 | |||||||
chr2:151413534 | A | T | 1 | a0003c0005t0007g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184-1289A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413534 | |||||||
chr2:151413560 | A | G | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1263A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413560 | |||||||
chr2:151413601 | A | G | 1 | a0001c0002t0001g0372 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.184-1222A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413601 | |||||||
chr2:151413629 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1194T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413629 | |||||||
chr2:151413638 | T | C | 1 | a0001c0007t0023g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-1185T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413638 | |||||||
chr2:151413641 | A | C | 1 | a0001c0003t0002g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.184-1182A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413641 | |||||||
chr2:151413682 | C | G | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.184-1141C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413682 | |||||||
chr2:151413720 | C | G | 1 | a0001c0009t0015g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-1103C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413720 | |||||||
chr2:151413743 | C | T | 2 | a0001c0007t0022g0274 a0001c0007t0022g0275 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.184-1080C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413743 | |||||||
chr2:151413749 | G | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.184-1074G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413749 | |||||||
chr2:151413785 | A | G | 1 | a0001c0009t0015g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-1038A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413785 | |||||||
chr2:151413833 | A | G | 5 | a0001c0004t0005g0086 a0001c0004t0005g0087 a0001c0004t0005g0089 others(2): Show |
5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-990A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413833 | |||||||
chr2:151414084 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-739G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414084 | |||||||
chr2:151414286 | CAAA | C | 112 | a0001c0003t0002g0002 a0002c0001t0003g0179 a0002c0001t0003g0187 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.184-525_184-523del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151414286 | ||||||
chr2:151414355 | T | C | 40 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(37): Show |
40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.184-468T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414355 | |||||||
chr2:151414450 | C | T | 1 | a0001c0009t0015g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184-373C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414450 | |||||||
chr2:151414507 | A | G | 3 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 |
3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.184-316A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414507 | |||||||
chr2:151414573 | T | C | 3 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 |
3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.184-250T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414573 | |||||||
chr2:151414613 | G | A | 1 | a0002c0001t0003g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184-210G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414613 | |||||||
chr2:151414674 | GTTTATT | G | 81 | a0001c0003t0002g0049 a0001c0003t0002g0050 a0001c0003t0002g0097 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.184-133_184-128del others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151414674 | ||||||
chr2:151414954 | G | A | 3 | a0002c0001t0019g0006 a0002c0001t0019g0007 a0002c0001t0019g0008 |
3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.280+35G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151414954 | |||||||
chr2:151415086 | G | A | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+167G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415086 | |||||||
chr2:151415196 | A | G | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.280+277A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415196 | |||||||
chr2:151415290 | T | C | 1 | a0001c0002t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.280+371T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415290 | |||||||
chr2:151415295 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+376C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415295 | |||||||
chr2:151415302 | G | A | 1 | a0001c0004t0005g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.280+383G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415302 | |||||||
chr2:151415345 | C | CA | 113 | a0001c0002t0001g0375 a0001c0003t0002g0002 a0001c0007t0023g0270 others(110): Show |
113 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.280+438dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415345 | ||||||
chr2:151415360 | A | G | 2 | a0002c0001t0026g0042 a0002c0001t0026g0043 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.280+441A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415360 | |||||||
chr2:151415393 | A | G | 112 | a0001c0003t0002g0002 a0002c0001t0003g0179 a0002c0001t0003g0187 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.280+474A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415393 | |||||||
chr2:151415399 | G | A | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280+480G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415399 | |||||||
chr2:151415535 | C | T | 1 | a0002c0001t0003g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+616C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415535 | |||||||
chr2:151415563 | C | CA | 10 | a0001c0002t0025g0195 a0001c0003t0002g0157 a0001c0003t0024g0267 others(7): Show |
10 | HG01069.hp2 HG01109.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+666dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAA | 150 | a0001c0002t0001g0001 a0001c0002t0001g0297 a0001c0002t0001g0298 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.280+665_280+666dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAAA | 29 | a0001c0002t0001g0178 a0001c0002t0001g0301 a0001c0002t0001g0303 others(26): Show |
29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.280+664_280+666dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAAAA | 10 | a0001c0003t0002g0099 a0001c0003t0002g0101 a0001c0003t0002g0102 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+663_280+666dup others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAAAAA | 35 | a0001c0003t0002g0097 a0001c0003t0037g0096 a0001c0004t0005g0052 others(32): Show |
35 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.280+662_280+666dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAAAAAA | 86 | a0001c0003t0002g0002 a0001c0004t0005g0062 a0001c0004t0005g0063 others(83): Show |
86 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.280+661_280+666dup others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415563 | C | CAAAAAAA | 24 | a0001c0004t0041g0053 a0002c0001t0003g0196 a0002c0001t0003g0200 others(21): Show |
24 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.280+660_280+666dup others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | ||||||
chr2:151415586 | G | A | 1 | a0002c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.280+667G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415586 | |||||||
chr2:151415590 | A | AT | 356 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(353): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.280+673dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415590 | ||||||
chr2:151415660 | G | C | 1 | a0001c0002t0001g0310 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.280+741G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415660 | |||||||
chr2:151415792 | G | A | 2 | a0001c0002t0001g0311 a0001c0002t0001g0312 |
2 | NA18951.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.281-769G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415792 | |||||||
chr2:151415807 | A | G | 263 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(260): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.281-754A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415807 | |||||||
chr2:151415883 | T | A | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-678T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415883 | |||||||
chr2:151416038 | T | A | 1 | a0001c0003t0002g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.281-523T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416038 | |||||||
chr2:151416139 | A | G | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.281-422A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416139 | |||||||
chr2:151416166 | T | G | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-395T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416166 | |||||||
chr2:151416304 | T | G | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-257T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416304 | |||||||
chr2:151416518 | G | A | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-43G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416518 | |||||||
chr2:151416969 | T | G | 1 | a0001c0003t0033g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.503+68T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151416969 | |||||||
chr2:151416989 | G | A | 261 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(258): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.503+88G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151416989 | |||||||
chr2:151417044 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+143T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417044 | |||||||
chr2:151417135 | T | C | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.503+234T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417135 | |||||||
chr2:151417244 | G | A | 353 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(350): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.503+343G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417244 | |||||||
chr2:151417303 | C | T | 5 | a0002c0001t0065g0239 a0006c0011t0014g0092 a0006c0011t0014g0093 others(2): Show |
5 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.503+402C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417303 | |||||||
chr2:151417310 | A | T | 3 | a0001c0002t0025g0194 a0001c0002t0025g0195 a0001c0022t0025g0193 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.503+409A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417310 | |||||||
chr2:151417311 | C | G | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.503+410C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417311 | |||||||
chr2:151417392 | C | A | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503+491C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417392 | |||||||
chr2:151417719 | G | A | 2 | a0002c0001t0012g0066 a0013c0026t0040g0051 |
2 | HG00639.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.503+818G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417719 | |||||||
chr2:151417892 | A | G | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.503+991A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417892 | |||||||
chr2:151418019 | GTATCTCA others(4): Show |
G | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.503+1121_503+1131d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418019 | ||||||
chr2:151418113 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+1212A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418113 | |||||||
chr2:151418330 | G | A | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.503+1429G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418330 | |||||||
chr2:151418447 | C | T | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503+1546C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418447 | |||||||
chr2:151418637 | G | A | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504-1553G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418637 | |||||||
chr2:151418760 | G | A | 3 | a0002c0001t0003g0204 a0002c0001t0003g0205 a0002c0001t0003g0206 |
3 | HG00544.hp1 NA18951.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.504-1430G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418760 | |||||||
chr2:151418790 | A | G | 262 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(259): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.504-1400A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418790 | |||||||
chr2:151418915 | A | G | 1 | a0003c0005t0007g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.504-1275A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418915 | |||||||
chr2:151418968 | C | CT | 7 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 others(4): Show |
7 | HG02280.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.504-1199dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | ||||||
chr2:151418968 | CT | C | 22 | a0001c0003t0002g0104 a0001c0003t0002g0110 a0001c0003t0002g0111 others(19): Show |
22 | HG00438.hp2 HG00558.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.504-1199delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | ||||||
chr2:151418968 | CTT | C | 297 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.504-1200_504-1199d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | ||||||
chr2:151418968 | CTTT | C | 25 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0315 others(22): Show |
25 | HG00280.hp2 HG00423.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.504-1201_504-1199d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | ||||||
chr2:151419010 | G | A | 1 | a0001c0003t0002g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.504-1180G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419010 | |||||||
chr2:151419087 | C | A | 1 | a0001c0009t0015g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.504-1103C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419087 | |||||||
chr2:151419098 | G | T | 20 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(17): Show |
20 | HG00597.hp1 HG00673.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.504-1092G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419098 | |||||||
chr2:151419388 | A | T | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-802A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419388 | |||||||
chr2:151419542 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.504-648T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419542 | |||||||
chr2:151419619 | C | G | 97 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(94): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.504-571C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419619 | |||||||
chr2:151419703 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.504-487G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419703 | |||||||
chr2:151419935 | A | G | 1 | a0002c0001t0065g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.504-255A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419935 | |||||||
chr2:151419990 | G | A | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-200G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419990 | |||||||
chr2:151420181 | C | G | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504-9C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151420181 | |||||||
chr2:151420494 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.693+115G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420494 | |||||||
chr2:151420635 | A | G | 373 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(370): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.693+256A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420635 | |||||||
chr2:151420691 | C | T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.693+312C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420691 | |||||||
chr2:151420734 | C | CA | 96 | a0001c0002t0001g0301 a0001c0002t0001g0317 a0001c0002t0001g0318 others(93): Show |
96 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.693+376dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | ||||||
chr2:151420734 | C | CAA | 6 | a0002c0001t0003g0187 a0002c0001t0003g0196 a0002c0001t0004g0048 others(3): Show |
6 | HG01884.hp1 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+375_693+376dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | ||||||
chr2:151420734 | CA | C | 130 | a0001c0002t0001g0312 a0001c0002t0001g0369 a0001c0002t0001g0370 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.693+376delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | ||||||
chr2:151420748 | A | G | 1 | a0001c0002t0001g0371 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.693+369A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420748 | |||||||
chr2:151420776 | T | G | 1 | a0002c0001t0067g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.693+397T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420776 | |||||||
chr2:151420779 | T | C | 12 | a0002c0001t0004g0010 a0002c0001t0004g0011 a0002c0001t0004g0012 others(9): Show |
12 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.693+400T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420779 | |||||||
chr2:151421166 | T | G | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.693+787T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421166 | |||||||
chr2:151421402 | C | G | 1 | a0001c0002t0045g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.693+1023C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421402 | |||||||
chr2:151421409 | A | G | 105 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.693+1030A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421409 | |||||||
chr2:151421588 | T | C | 111 | a0002c0001t0003g0179 a0002c0001t0003g0187 a0002c0001t0003g0188 others(108): Show |
111 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.693+1209T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421588 | |||||||
chr2:151421629 | C | T | 2 | a0005c0010t0018g0246 a0005c0010t0018g0247 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.693+1250C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421629 | |||||||
chr2:151421649 | A | G | 8 | a0001c0002t0001g0368 a0005c0010t0018g0183 a0005c0010t0018g0184 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+1270A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421649 | |||||||
chr2:151421694 | G | A | 1 | a0002c0001t0004g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.694-1256G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421694 | |||||||
chr2:151421753 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1197G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421753 | |||||||
chr2:151421837 | AT | A | 8 | a0001c0002t0001g0298 a0001c0003t0002g0174 a0001c0004t0006g0071 others(5): Show |
8 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1098delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151421837 | ||||||
chr2:151421895 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1055C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421895 | |||||||
chr2:151421900 | T | C | 116 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.694-1050T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421900 | |||||||
chr2:151422081 | C | T | 2 | a0002c0001t0004g0013 a0002c0001t0004g0026 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694-869C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422081 | |||||||
chr2:151422148 | C | T | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-802C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422148 | |||||||
chr2:151422644 | C | T | 2 | a0002c0001t0010g0208 a0002c0001t0010g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.694-306C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422644 | |||||||
chr2:151422769 | A | G | 161 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.694-181A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422769 | |||||||
chr2:151423131 | A | T | 3 | a0002c0001t0003g0240 a0002c0001t0003g0241 a0002c0001t0003g0272 |
3 | HG00738.hp2 HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.786+89A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423131 | |||||||
chr2:151423487 | C | G | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.786+445C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423487 | |||||||
chr2:151423521 | T | C | 1 | a0002c0001t0004g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.786+479T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423521 | |||||||
chr2:151423581 | T | G | 2 | a0002c0001t0003g0188 a0002c0001t0003g0189 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.786+539T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423581 | |||||||
chr2:151423732 | A | G | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.786+690A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423732 | |||||||
chr2:151423851 | G | A | 158 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.786+809G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423851 | |||||||
chr2:151424006 | C | T | 1 | a0019c0033t0003g0202 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786+964C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424006 | |||||||
chr2:151424012 | GTC | G | 8 | a0002c0001t0008g0009 a0002c0001t0008g0018 a0002c0001t0008g0032 others(5): Show |
8 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+974_786+975del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424012 | ||||||
chr2:151424125 | C | T | 1 | a0001c0003t0002g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.786+1083C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424125 | |||||||
chr2:151424126 | G | A | 1 | a0018c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.786+1084G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424126 | |||||||
chr2:151424147 | A | T | 40 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(37): Show |
40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.786+1105A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424147 | |||||||
chr2:151424260 | T | C | 2 | a0001c0002t0013g0175 a0016c0023t0001g0319 |
2 | HG01106.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.786+1218T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424260 | |||||||
chr2:151424265 | G | A | 1 | a0002c0001t0010g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.786+1223G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424265 | |||||||
chr2:151424706 | A | G | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.786+1664A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424706 | |||||||
chr2:151424825 | A | AT | 62 | a0001c0003t0002g0109 a0001c0003t0002g0120 a0001c0003t0002g0144 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.786+1814dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | A | ATT | 36 | a0001c0003t0002g0049 a0001c0003t0002g0050 a0001c0003t0002g0121 others(33): Show |
36 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.786+1813_786+1814d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | A | ATTT | 7 | a0002c0001t0003g0241 a0002c0001t0003g0272 a0002c0001t0003g0277 others(4): Show |
7 | HG01109.hp1 HG02056.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1812_786+1814d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | A | ATTTTT | 7 | a0001c0003t0033g0113 a0003c0005t0007g0279 a0003c0005t0007g0288 others(4): Show |
7 | HG02165.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1810_786+1814d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | A | ATTTTTT | 7 | a0003c0005t0007g0278 a0003c0005t0007g0280 a0003c0005t0007g0281 others(4): Show |
7 | HG01175.hp1 HG02145.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+1809_786+1814d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | AT | A | 12 | a0001c0002t0001g0318 a0001c0002t0001g0364 a0001c0002t0001g0365 others(9): Show |
12 | HG01433.hp2 HG01517.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+1814delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATT | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0305 others(37): Show |
41 | HG00323.hp2 HG00438.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.786+1813_786+1814d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTT | A | 52 | a0001c0002t0001g0297 a0001c0002t0001g0298 a0001c0002t0001g0301 others(49): Show |
52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.786+1812_786+1814d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(3): Show |
A | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+1805_786+1814d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(4): Show |
A | 2 | a0002c0001t0003g0240 a0003c0005t0007g0286 |
2 | HG00738.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.786+1804_786+1814d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(6): Show |
A | 14 | a0001c0003t0002g0105 a0001c0003t0002g0106 a0001c0003t0002g0111 others(11): Show |
14 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+1802_786+1814d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(7): Show |
A | 1 | a0001c0003t0002g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.786+1801_786+1814d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(8): Show |
A | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.786+1800_786+1814d others(17): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424825 | ATTTTTTT others(9): Show |
A | 1 | a0001c0003t0002g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.786+1799_786+1814d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | ||||||
chr2:151424840 | TTTTTTTT others(10): Show |
T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786+1799_786+1815d others(19): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424840 | |||||||
chr2:151424841 | T | C | 1 | a0001c0004t0006g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+1799T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424841 | |||||||
chr2:151424843 | TTTTTTTT others(7): Show |
T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+1802_786+1815d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424843 | |||||||
chr2:151424844 | TTTTTTTT others(6): Show |
T | 1 | a0001c0004t0006g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+1803_786+1815d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424844 | |||||||
chr2:151424850 | T | C | 38 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(35): Show |
38 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.786+1808T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424850 | |||||||
chr2:151424853 | TTTTC | T | 39 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1812_786+1815d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424853 | |||||||
chr2:151424877 | G | C | 116 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.786+1835G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424877 | |||||||
chr2:151424895 | C | G | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786+1853C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424895 | |||||||
chr2:151424983 | C | T | 2 | a0002c0001t0026g0042 a0002c0001t0026g0043 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.786+1941C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424983 | |||||||
chr2:151425007 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+1965C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425007 | |||||||
chr2:151425042 | C | T | 1 | a0001c0004t0006g0070 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.786+2000C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425042 | |||||||
chr2:151425047 | C | G | 83 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.786+2005C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425047 | |||||||
chr2:151425126 | T | C | 1 | a0002c0001t0010g0208 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786+2084T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425126 | |||||||
chr2:151425216 | C | CT | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+2175dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425216 | ||||||
chr2:151425421 | A | C | 266 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.786+2379A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425421 | |||||||
chr2:151425531 | A | G | 3 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 |
3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.786+2489A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425531 | |||||||
chr2:151425550 | T | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.786+2508T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425550 | |||||||
chr2:151425647 | T | A | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.786+2605T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425647 | |||||||
chr2:151425660 | C | CT | 173 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(170): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.786+2640dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | ||||||
chr2:151425660 | C | CTT | 68 | a0001c0002t0001g0376 a0001c0003t0002g0106 a0001c0003t0002g0119 others(65): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.786+2639_786+2640d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | ||||||
chr2:151425660 | C | CTTT | 83 | a0001c0002t0001g0001 a0001c0002t0001g0297 a0001c0002t0001g0298 others(80): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.786+2638_786+2640d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | ||||||
chr2:151425660 | C | CTTTT | 24 | a0001c0002t0001g0178 a0001c0002t0001g0304 a0001c0002t0001g0307 others(21): Show |
24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.786+2637_786+2640d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | ||||||
chr2:151425877 | C | G | 1 | a0001c0002t0048g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786+2835C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425877 | |||||||
chr2:151425942 | G | A | 1 | a0001c0003t0037g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.787-2842G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425942 | |||||||
chr2:151425969 | G | A | 1 | a0025c0025t0001g0360 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.787-2815G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425969 | |||||||
chr2:151426080 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2704T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426080 | |||||||
chr2:151426167 | A | ATTTTTTT others(4): Show |
1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.787-2617_787-2616i others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426167 | |||||||
chr2:151426168 | A | AT | 11 | a0002c0001t0003g0203 a0002c0001t0003g0227 a0002c0001t0004g0028 others(8): Show |
11 | HG00639.hp2 HG02056.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2592dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTT | 88 | a0001c0003t0002g0002 a0001c0003t0002g0050 a0001c0003t0002g0097 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.787-2594_787-2592d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTT | 37 | a0001c0002t0025g0194 a0001c0003t0002g0049 a0001c0003t0002g0106 others(34): Show |
37 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.787-2595_787-2592d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT | 17 | a0001c0002t0001g0303 a0001c0002t0001g0313 a0001c0002t0001g0320 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.787-2598_787-2592d others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(1): Show |
34 | a0001c0002t0001g0001 a0001c0002t0001g0300 a0001c0002t0001g0304 others(31): Show |
35 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.787-2599_787-2592d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(2): Show |
24 | a0001c0002t0001g0178 a0001c0002t0001g0297 a0001c0002t0001g0301 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.787-2600_787-2592d others(11): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(3): Show |
10 | a0001c0002t0001g0298 a0001c0002t0001g0337 a0001c0002t0001g0339 others(7): Show |
10 | HG01993.hp2 HG02071.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.787-2601_787-2592d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(4): Show |
5 | a0001c0002t0001g0340 a0001c0002t0001g0343 a0001c0002t0052g0342 others(2): Show |
5 | HG00558.hp1 HG02080.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-2602_787-2592d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(5): Show |
1 | a0001c0002t0025g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.787-2603_787-2592d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(6): Show |
1 | a0001c0022t0025g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.787-2604_787-2592d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0308 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.787-2605_787-2592d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(8): Show |
14 | a0001c0004t0005g0062 a0001c0004t0005g0065 a0001c0004t0005g0078 others(11): Show |
14 | HG02056.hp2 HG03492.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.787-2606_787-2592d others(17): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(9): Show |
7 | a0001c0004t0005g0086 a0001c0004t0006g0056 a0001c0004t0006g0057 others(4): Show |
7 | HG03041.hp2 NA18945.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.787-2607_787-2592d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(10): Show |
4 | a0001c0004t0005g0079 a0001c0004t0006g0054 a0001c0004t0006g0058 others(1): Show |
4 | HG00673.hp1 HG02071.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-2608_787-2592d others(19): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(11): Show |
3 | a0001c0004t0006g0060 a0001c0004t0006g0075 a0001c0007t0022g0275 |
3 | HG02132.hp2 HG02965.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.787-2609_787-2592d others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(14): Show |
1 | a0001c0004t0006g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.787-2612_787-2592d others(23): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(15): Show |
1 | a0001c0004t0006g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.787-2613_787-2592d others(24): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(21): Show |
1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787-2592_787-2591i others(30): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | ATTTTTTT others(27): Show |
1 | a0001c0004t0006g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.787-2592_787-2591i others(36): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | A | T | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.787-2616A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426168 | |||||||
chr2:151426168 | AT | A | 11 | a0002c0001t0003g0254 a0002c0001t0003g0257 a0002c0001t0003g0273 others(8): Show |
11 | HG01070.hp2 HG01109.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2592delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426168 | ATTTT | A | 6 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(3): Show |
6 | HG00609.hp1 HG02040.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2595_787-2592d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | ||||||
chr2:151426219 | G | A | 1 | a0001c0004t0005g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.787-2565G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426219 | |||||||
chr2:151426223 | G | A | 1 | a0001c0003t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.787-2561G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426223 | |||||||
chr2:151426323 | C | T | 105 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.787-2461C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426323 | |||||||
chr2:151426407 | C | A | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2377C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426407 | |||||||
chr2:151426659 | G | GT | 13 | a0001c0003t0002g0143 a0001c0003t0024g0266 a0001c0003t0024g0267 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-2115dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426659 | ||||||
chr2:151426660 | T | G | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-2124T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426660 | |||||||
chr2:151426660 | T | TTTTTTTT others(3): Show |
1 | a0002c0001t0010g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.787-2114_787-2105d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426660 | ||||||
chr2:151426685 | C | T | 105 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.787-2099C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426685 | |||||||
chr2:151426841 | T | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-1943T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426841 | |||||||
chr2:151426946 | C | G | 1 | a0001c0003t0002g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.787-1838C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426946 | |||||||
chr2:151427058 | T | A | 3 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 |
3 | HG02965.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.787-1726T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427058 | |||||||
chr2:151427102 | G | A | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-1682G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427102 | |||||||
chr2:151427103 | C | A | 3 | a0001c0002t0025g0194 a0001c0002t0025g0195 a0001c0022t0025g0193 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.787-1681C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427103 | |||||||
chr2:151427174 | C | A | 1 | a0003c0005t0007g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-1610C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427174 | |||||||
chr2:151427259 | C | T | 17 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(14): Show |
17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.787-1525C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427259 | |||||||
chr2:151427378 | T | G | 1 | a0001c0002t0001g0340 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.787-1406T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427378 | |||||||
chr2:151427431 | G | A | 1 | a0002c0001t0010g0235 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.787-1353G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427431 | |||||||
chr2:151427500 | C | T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.787-1284C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427500 | |||||||
chr2:151427525 | A | AT | 114 | a0001c0002t0001g0366 a0001c0003t0002g0002 a0001c0003t0002g0049 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.787-1248dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151427525 | ||||||
chr2:151427746 | A | G | 1 | a0001c0002t0001g0371 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-1038A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427746 | |||||||
chr2:151427873 | A | G | 1 | a0002c0001t0004g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-911A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427873 | |||||||
chr2:151427972 | G | A | 1 | a0001c0003t0002g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.787-812G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427972 | |||||||
chr2:151428008 | G | A | 1 | a0006c0011t0014g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.787-776G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428008 | |||||||
chr2:151428020 | G | A | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-764G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428020 | |||||||
chr2:151428030 | C | T | 2 | a0001c0002t0025g0194 a0001c0002t0025g0195 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.787-754C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428030 | |||||||
chr2:151428055 | CAAACA | C | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-710_787-706del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151428055 | ||||||
chr2:151428122 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-662G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428122 | |||||||
chr2:151428215 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-569C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428215 | |||||||
chr2:151428307 | T | A | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-477T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428307 | |||||||
chr2:151428446 | G | A | 1 | a0001c0002t0051g0363 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.787-338G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428446 | |||||||
chr2:151428508 | CTG | C | 39 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.787-272_787-271del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151428508 | ||||||
chr2:151428585 | T | C | 1 | a0002c0001t0010g0208 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.787-199T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428585 | |||||||
chr2:151428630 | A | G | 2 | a0001c0003t0027g0114 a0001c0003t0027g0115 |
2 | NA18957.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.787-154A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428630 | |||||||
chr2:151428681 | G | A | 3 | a0001c0003t0002g0109 a0001c0003t0002g0124 a0001c0003t0002g0136 |
3 | HG00738.hp1 HG02148.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.787-103G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428681 | |||||||
chr2:151428776 | C | A | 1 | a0001c0002t0021g0324 | 1 | NA18990.hp2 | splice_region_variant&intron_variant | LOW | c.787-8C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428776 | |||||||
chr2:151429034 | A | C | 1 | a0002c0001t0070g0003 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.925+112A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429034 | |||||||
chr2:151429101 | G | A | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+179G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429101 | |||||||
chr2:151429214 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.925+292G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429214 | |||||||
chr2:151429305 | C | T | 1 | a0002c0001t0038g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.925+383C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429305 | |||||||
chr2:151429306 | G | C | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.925+384G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429306 | |||||||
chr2:151429460 | G | A | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.925+538G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429460 | |||||||
chr2:151429777 | A | C | 1 | a0001c0003t0002g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.925+855A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429777 | |||||||
chr2:151429863 | G | A | 2 | a0002c0001t0003g0276 a0002c0001t0003g0277 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.925+941G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429863 | |||||||
chr2:151430177 | C | T | 1 | a0001c0003t0034g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.925+1255C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430177 | |||||||
chr2:151430249 | C | T | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+1327C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430249 | |||||||
chr2:151430278 | CCCAAAGT others(9): Show |
C | 1 | a0002c0001t0020g0030 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.925+1360_925+1375d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430278 | ||||||
chr2:151430320 | C | CT | 7 | a0001c0004t0006g0057 a0005c0010t0018g0183 a0005c0010t0018g0184 others(4): Show |
7 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+1406dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430320 | ||||||
chr2:151430424 | C | T | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.925+1502C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430424 | |||||||
chr2:151430431 | C | T | 2 | a0005c0010t0018g0183 a0005c0010t0018g0184 |
2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.925+1509C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430431 | |||||||
chr2:151430453 | C | T | 1 | a0001c0002t0013g0095 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.925+1531C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430453 | |||||||
chr2:151430479 | G | A | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.925+1557G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430479 | |||||||
chr2:151430488 | A | G | 1 | a0003c0005t0007g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925+1566A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430488 | |||||||
chr2:151430666 | T | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+1744T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430666 | |||||||
chr2:151430669 | C | T | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.925+1747C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430669 | |||||||
chr2:151430712 | G | A | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.925+1790G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430712 | |||||||
chr2:151430751 | C | T | 1 | a0001c0003t0002g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.925+1829C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430751 | |||||||
chr2:151430771 | GC | G | 263 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.925+1856delC | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430771 | ||||||
chr2:151430866 | C | G | 3 | a0009c0014t0001g0377 a0009c0014t0001g0378 a0009c0014t0001g0379 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.925+1944C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430866 | |||||||
chr2:151431317 | A | G | 117 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.926-1760A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431317 | |||||||
chr2:151431361 | C | T | 1 | a0001c0002t0001g0331 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.926-1716C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431361 | |||||||
chr2:151431362 | G | C | 19 | a0001c0002t0001g0001 a0001c0002t0001g0305 a0001c0002t0001g0307 others(16): Show |
20 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.926-1715G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431362 | |||||||
chr2:151431383 | A | C | 118 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.926-1694A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431383 | |||||||
chr2:151431579 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-1498C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431579 | |||||||
chr2:151431726 | C | T | 6 | a0001c0002t0025g0194 a0001c0002t0025g0195 a0006c0011t0014g0092 others(3): Show |
6 | HG00423.hp2 HG00609.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-1351C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431726 | |||||||
chr2:151431727 | G | A | 1 | a0002c0001t0003g0237 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.926-1350G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431727 | |||||||
chr2:151431779 | C | CTGAA | 51 | a0001c0002t0001g0313 a0001c0002t0001g0372 a0001c0002t0013g0173 others(48): Show |
51 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.926-1265_926-1262d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | ||||||
chr2:151431779 | C | CTGAATGA others(1): Show |
135 | a0001c0002t0001g0178 a0001c0002t0001g0297 a0001c0002t0001g0298 others(132): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.926-1269_926-1262d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | ||||||
chr2:151431779 | C | CTGAATGA others(5): Show |
51 | a0001c0002t0001g0001 a0001c0002t0001g0305 a0001c0002t0001g0307 others(48): Show |
52 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.926-1273_926-1262d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | ||||||
chr2:151431779 | C | CTGAATGA others(9): Show |
5 | a0001c0002t0001g0311 a0001c0002t0001g0355 a0001c0002t0047g0357 others(2): Show |
5 | HG00140.hp1 HG00621.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-1277_926-1262d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | ||||||
chr2:151431779 | CTGAA | C | 47 | a0001c0003t0002g0130 a0001c0009t0015g0250 a0002c0001t0003g0196 others(44): Show |
47 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.926-1265_926-1262d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | ||||||
chr2:151431816 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-1261C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431816 | |||||||
chr2:151431822 | G | A | 1 | a0001c0004t0006g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.926-1255G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431822 | |||||||
chr2:151432047 | C | G | 1 | a0001c0004t0005g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.926-1030C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432047 | |||||||
chr2:151432064 | A | C | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-1013A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432064 | |||||||
chr2:151432100 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-977C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432100 | |||||||
chr2:151432145 | A | G | 1 | a0001c0002t0001g0343 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.926-932A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432145 | |||||||
chr2:151432154 | G | T | 1 | a0001c0002t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.926-923G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432154 | |||||||
chr2:151432156 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-921C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432156 | |||||||
chr2:151432220 | G | A | 4 | a0002c0001t0004g0037 a0002c0001t0004g0039 a0002c0001t0004g0040 others(1): Show |
4 | NA18957.hp1 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-857G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432220 | |||||||
chr2:151432265 | C | T | 1 | a0001c0003t0002g0143 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.926-812C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432265 | |||||||
chr2:151432623 | G | T | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.926-454G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432623 | |||||||
chr2:151432703 | G | T | 1 | a0001c0002t0021g0324 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-374G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432703 | |||||||
chr2:151432873 | T | C | 1 | a0001c0002t0001g0326 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.926-204T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432873 | |||||||
chr2:151433011 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-66T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433011 | |||||||
chr2:151433043 | C | T | 3 | a0007c0012t0007g0290 a0007c0012t0007g0291 a0007c0012t0007g0294 |
3 | HG01175.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.926-34C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433043 | |||||||
chr2:151433049 | T | G | 3 | a0002c0001t0012g0066 a0002c0001t0012g0068 a0002c0001t0012g0069 |
3 | NA18968.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.926-28T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433049 | |||||||
chr2:151433253 | G | A | 82 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1077+25G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433253 | |||||||
chr2:151433256 | C | T | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1077+28C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433256 | |||||||
chr2:151433313 | T | C | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1077+85T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433313 | |||||||
chr2:151433318 | G | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+90G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433318 | |||||||
chr2:151433393 | A | G | 2 | a0001c0003t0002g0109 a0001c0003t0002g0136 |
2 | HG00738.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1077+165A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433393 | |||||||
chr2:151433440 | T | A | 3 | a0001c0002t0001g0329 a0001c0002t0001g0330 a0001c0002t0001g0362 |
3 | NA18980.hp1 NA19056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1077+212T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433440 | |||||||
chr2:151433603 | C | T | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1077+375C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433603 | |||||||
chr2:151433604 | G | A | 105 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1077+376G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433604 | |||||||
chr2:151433653 | C | T | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+425C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433653 | |||||||
chr2:151433675 | G | A | 1 | a0001c0007t0022g0274 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1077+447G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433675 | |||||||
chr2:151433681 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1077+453C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433681 | |||||||
chr2:151433747 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1077+519G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433747 | |||||||
chr2:151433859 | G | A | 1 | a0001c0003t0024g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1077+631G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433859 | |||||||
chr2:151433867 | C | A | 1 | a0002c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1077+639C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433867 | |||||||
chr2:151433871 | C | T | 1 | a0001c0002t0001g0325 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1077+643C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433871 | |||||||
chr2:151433874 | C | T | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077+646C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433874 | |||||||
chr2:151433909 | T | C | 272 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1077+681T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433909 | |||||||
chr2:151433930 | G | A | 1 | a0001c0004t0005g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1077+702G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433930 | |||||||
chr2:151433969 | T | G | 36 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(33): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1077+741T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433969 | |||||||
chr2:151434100 | G | A | 4 | a0001c0002t0001g0297 a0001c0002t0001g0331 a0001c0002t0001g0346 others(1): Show |
4 | HG00642.hp1 HG01099.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+872G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434100 | |||||||
chr2:151434167 | C | CA | 92 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1077+954dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434167 | ||||||
chr2:151434167 | C | CAA | 7 | a0001c0002t0001g0337 a0001c0009t0015g0250 a0001c0009t0015g0251 others(4): Show |
7 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+953_1077+954d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434167 | ||||||
chr2:151434167 | C | G | 2 | a0001c0004t0006g0059 a0001c0004t0006g0071 |
2 | HG01358.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1077+939C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434167 | |||||||
chr2:151434179 | AAAAG | A | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+953_1077+956d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434179 | ||||||
chr2:151434181 | A | AG | 3 | a0001c0002t0001g0343 a0001c0002t0001g0347 a0001c0002t0013g0095 |
3 | NA18940.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1077+953_1077+954i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434181 | |||||||
chr2:151434331 | C | T | 1 | a0002c0001t0004g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1077+1103C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434331 | |||||||
chr2:151434415 | T | C | 1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1078-1048T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434415 | |||||||
chr2:151434430 | T | C | 1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1078-1033T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434430 | |||||||
chr2:151434437 | A | AT | 41 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(38): Show |
41 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1078-1005dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | A | ATT | 8 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(5): Show |
8 | HG01175.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1078-1006_1078-100 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | A | ATTT | 9 | a0001c0003t0002g0126 a0001c0003t0002g0131 a0001c0003t0011g0116 others(6): Show |
9 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-1007_1078-100 others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | A | ATTTT | 63 | a0001c0003t0002g0050 a0001c0003t0002g0097 a0001c0003t0002g0099 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1078-1008_1078-100 others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | A | ATTTTT | 13 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0108 others(10): Show |
13 | HG00597.hp2 HG00621.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-1009_1078-100 others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | AT | A | 101 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1078-1005delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434437 | ATT | A | 37 | a0001c0002t0001g0369 a0001c0004t0005g0052 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1078-1006_1078-100 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | ||||||
chr2:151434586 | G | A | 2 | a0001c0002t0001g0325 a0001c0002t0001g0365 |
2 | NA18977.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1078-877G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434586 | |||||||
chr2:151434786 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-677C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434786 | |||||||
chr2:151434955 | A | G | 2 | a0001c0003t0057g0262 a0001c0003t0058g0261 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1078-508A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434955 | |||||||
chr2:151435018 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-445C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435018 | |||||||
chr2:151435085 | T | C | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-378T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435085 | |||||||
chr2:151435098 | A | G | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1078-365A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435098 | |||||||
chr2:151435270 | C | A | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1078-193C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435270 | |||||||
chr2:151435310 | C | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-153C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435310 | |||||||
chr2:151435601 | T | G | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1195+21T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435601 | |||||||
chr2:151435609 | T | C | 1 | a0002c0001t0012g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1195+29T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435609 | |||||||
chr2:151435655 | GA | G | 117 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.1195+84delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435655 | ||||||
chr2:151435708 | C | T | 1 | a0001c0003t0002g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1195+128C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435708 | |||||||
chr2:151435722 | T | C | 2 | a0002c0001t0004g0014 a0002c0001t0004g0021 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1195+142T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435722 | |||||||
chr2:151435747 | A | G | 4 | a0002c0001t0004g0037 a0002c0001t0004g0039 a0002c0001t0004g0040 others(1): Show |
4 | NA18957.hp1 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195+167A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435747 | |||||||
chr2:151435760 | G | GT | 33 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(30): Show |
33 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1195+186dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435760 | ||||||
chr2:151435767 | G | GT | 7 | a0001c0002t0001g0312 a0001c0002t0021g0350 a0001c0003t0002g0119 others(4): Show |
7 | HG00621.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+199dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435767 | ||||||
chr2:151435767 | G | T | 41 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(38): Show |
41 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1195+187G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435767 | |||||||
chr2:151435768 | T | G | 8 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(5): Show |
8 | HG01891.hp2 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+188T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435768 | |||||||
chr2:151435804 | C | T | 1 | a0002c0001t0020g0030 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1195+224C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435804 | |||||||
chr2:151435834 | T | G | 2 | a0001c0002t0013g0175 a0016c0023t0001g0319 |
2 | HG01106.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1195+254T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435834 | |||||||
chr2:151435893 | G | A | 264 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1195+313G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435893 | |||||||
chr2:151436080 | C | T | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1195+500C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436080 | |||||||
chr2:151436125 | T | G | 1 | a0002c0001t0003g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1195+545T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436125 | |||||||
chr2:151436132 | G | A | 2 | a0005c0010t0018g0183 a0005c0010t0018g0184 |
2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1195+552G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436132 | |||||||
chr2:151436213 | G | A | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1196-614G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436213 | |||||||
chr2:151436225 | C | T | 4 | a0001c0004t0006g0055 a0001c0004t0006g0056 a0001c0004t0006g0067 others(1): Show |
4 | NA18945.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196-602C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436225 | |||||||
chr2:151436484 | T | G | 1 | a0002c0001t0003g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1196-343T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436484 | |||||||
chr2:151436540 | C | CA | 32 | a0001c0002t0001g0306 a0001c0002t0001g0318 a0001c0002t0001g0332 others(29): Show |
32 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1196-267dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436540 | ||||||
chr2:151436540 | CA | C | 10 | a0001c0002t0001g0358 a0001c0002t0013g0175 a0001c0002t0021g0350 others(7): Show |
10 | HG01515.hp2 HG01993.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-267delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436540 | ||||||
chr2:151436578 | T | C | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1196-249T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436578 | |||||||
chr2:151436683 | A | G | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-144A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436683 | |||||||
chr2:151436685 | ATTAATAT others(1): Show |
A | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1196-140_1196-133d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436685 | ||||||
chr2:151436741 | G | C | 1 | a0001c0002t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1196-86G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436741 | |||||||
chr2:151436819 | T | C | 1 | a0001c0002t0025g0195 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.1196-8T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436819 | |||||||
chr2:151437039 | A | C | 17 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(14): Show |
17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1372+36A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/35 | chr2 | 151437039 | |||||||
chr2:151437106 | C | T | 264 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1372+103C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/35 | chr2 | 151437106 | |||||||
chr2:151437592 | G | A | 1 | a0002c0001t0067g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1483+241G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151437592 | |||||||
chr2:151437927 | G | T | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483+576G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151437927 | |||||||
chr2:151438038 | T | G | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1484-646T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438038 | |||||||
chr2:151438237 | GGA | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-443_1484-442d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr2 | 151438237 | ||||||
chr2:151438420 | A | G | 1 | a0001c0003t0034g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1484-264A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438420 | |||||||
chr2:151438474 | G | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-210G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438474 | |||||||
chr2:151438518 | G | A | 1 | a0018c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1484-166G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438518 | |||||||
chr2:151438561 | AAAATT | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-115_1484-111d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr2 | 151438561 | ||||||
chr2:151438627 | A | G | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1484-57A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438627 | |||||||
chr2:151438783 | A | C | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+37A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438783 | |||||||
chr2:151438791 | G | A | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+45G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438791 | |||||||
chr2:151438817 | C | A | 1 | a0003c0005t0007g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1546+71C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438817 | |||||||
chr2:151438817 | C | G | 5 | a0001c0002t0001g0335 a0001c0002t0001g0339 a0001c0002t0001g0343 others(2): Show |
5 | HG00280.hp1 NA18940.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+71C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438817 | |||||||
chr2:151438892 | G | A | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1546+146G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438892 | |||||||
chr2:151438937 | C | T | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+191C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438937 | |||||||
chr2:151438958 | A | G | 2 | a0001c0003t0057g0262 a0001c0003t0058g0261 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+212A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438958 | |||||||
chr2:151439001 | A | G | 1 | a0002c0001t0003g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1546+255A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439001 | |||||||
chr2:151439054 | C | T | 365 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(362): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1546+308C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439054 | |||||||
chr2:151439108 | G | T | 1 | a0001c0003t0055g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1546+362G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439108 | |||||||
chr2:151439154 | C | T | 1 | a0002c0001t0004g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1546+408C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439154 | |||||||
chr2:151439348 | T | C | 5 | a0001c0003t0002g0121 a0001c0003t0002g0122 a0001c0003t0002g0174 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+602T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439348 | |||||||
chr2:151439392 | C | T | 1 | a0001c0002t0001g0335 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1547-635C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439392 | |||||||
chr2:151439476 | C | T | 3 | a0002c0001t0004g0016 a0002c0001t0004g0020 a0002c0001t0038g0027 |
3 | HG03471.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1547-551C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439476 | |||||||
chr2:151439481 | A | G | 2 | a0002c0001t0010g0208 a0002c0001t0010g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1547-546A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439481 | |||||||
chr2:151439561 | C | G | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-466C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439561 | |||||||
chr2:151439629 | A | G | 2 | a0001c0003t0002g0120 a0001c0003t0002g0151 |
2 | HG02523.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1547-398A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439629 | |||||||
chr2:151439667 | C | CA | 79 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(76): Show |
79 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1547-343dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439667 | ||||||
chr2:151439696 | A | G | 1 | a0001c0002t0001g0312 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1547-331A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439696 | |||||||
chr2:151439972 | C | CA | 84 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0298 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1547-32dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAA | 17 | a0001c0002t0001g0297 a0001c0002t0001g0308 a0001c0002t0001g0316 others(14): Show |
17 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-33_1547-32dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAA | 6 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1547-34_1547-32dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAA | 15 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0023g0270 others(12): Show |
15 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1547-35_1547-32dup others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAAA | 11 | a0001c0003t0057g0262 a0001c0007t0022g0275 a0001c0007t0023g0263 others(8): Show |
11 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-36_1547-32dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAAAAA | 56 | a0001c0003t0002g0002 a0001c0003t0002g0097 a0001c0003t0002g0099 others(53): Show |
56 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1547-38_1547-32dup others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAAAAA others(1): Show |
15 | a0001c0003t0002g0050 a0001c0003t0002g0101 a0001c0003t0002g0102 others(12): Show |
15 | HG00558.hp2 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1547-39_1547-32dup others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAAAAA others(2): Show |
8 | a0001c0003t0002g0049 a0001c0003t0002g0122 a0001c0003t0002g0132 others(5): Show |
8 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547-40_1547-32dup others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | C | CAAAAAAA others(3): Show |
4 | a0001c0003t0002g0168 a0001c0003t0028g0140 a0001c0003t0028g0141 others(1): Show |
4 | HG01123.hp2 HG02602.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-41_1547-32dup others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151439972 | CA | C | 11 | a0001c0004t0005g0086 a0001c0022t0025g0193 a0002c0001t0003g0221 others(8): Show |
11 | HG01081.hp2 HG01099.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-32delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | ||||||
chr2:151440221 | CTT | C | 4 | a0002c0001t0026g0015 a0002c0001t0026g0042 a0002c0001t0026g0043 others(1): Show |
4 | HG01192.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+99_1647+100de others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr2 | 151440221 | ||||||
chr2:151440326 | A | G | 2 | a0003c0005t0007g0284 a0003c0005t0007g0285 |
2 | HG00639.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1647+199A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440326 | |||||||
chr2:151440378 | A | G | 36 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(33): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1647+251A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440378 | |||||||
chr2:151440385 | G | A | 2 | a0001c0003t0002g0111 a0001c0003t0002g0153 |
2 | HG03831.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1647+258G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440385 | |||||||
chr2:151440397 | G | A | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1647+270G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440397 | |||||||
chr2:151440482 | A | C | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1647+355A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440482 | |||||||
chr2:151440540 | C | G | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+413C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440540 | |||||||
chr2:151440570 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1647+443G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440570 | |||||||
chr2:151440658 | T | C | 273 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1647+531T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440658 | |||||||
chr2:151440850 | A | T | 3 | a0001c0002t0001g0366 a0001c0002t0001g0368 a0025c0025t0001g0360 |
3 | NA18989.hp2 NA19007.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1647+723A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440850 | |||||||
chr2:151440853 | C | T | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1647+726C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440853 | |||||||
chr2:151440918 | G | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+791G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440918 | |||||||
chr2:151441260 | C | T | 5 | a0002c0001t0003g0227 a0002c0001t0003g0254 a0002c0001t0003g0255 others(2): Show |
5 | HG01070.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-645C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441260 | |||||||
chr2:151441274 | C | T | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648-631C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441274 | |||||||
chr2:151441433 | A | G | 8 | a0002c0001t0003g0191 a0002c0001t0003g0200 a0002c0001t0003g0207 others(5): Show |
8 | HG02056.hp1 HG02083.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648-472A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441433 | |||||||
chr2:151441506 | G | T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1648-399G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441506 | |||||||
chr2:151441526 | T | C | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1648-379T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441526 | |||||||
chr2:151441737 | T | C | 1 | a0002c0001t0012g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1648-168T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441737 | |||||||
chr2:151441801 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1648-104G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441801 | |||||||
chr2:151441841 | C | T | 1 | a0002c0001t0066g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1648-64C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441841 | |||||||
chr2:151442048 | T | TTTTTA | 97 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(94): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1734+91_1734+95dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | T | TTTTTATT others(3): Show |
109 | a0001c0002t0001g0329 a0001c0002t0001g0330 a0001c0002t0001g0358 others(106): Show |
109 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1734+86_1734+95dup others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | T | TTTTTATT others(8): Show |
93 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1734+81_1734+95dup others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | T | TTTTTATT others(13): Show |
56 | a0001c0003t0002g0105 a0001c0003t0002g0117 a0001c0003t0011g0116 others(53): Show |
56 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1734+76_1734+95dup others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | T | TTTTTATT others(18): Show |
4 | a0001c0004t0006g0070 a0001c0004t0006g0073 a0001c0004t0006g0076 others(1): Show |
4 | HG00544.hp2 NA18998.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+71_1734+95dup others(25): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | T | TTTTTGTT others(13): Show |
1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1734+61_1734+62ins others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442048 | TTTTTA | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0177 others(1): Show |
4 | HG00609.hp1 HG02040.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+91_1734+95del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | ||||||
chr2:151442237 | G | A | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1734+246G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442237 | |||||||
chr2:151442362 | T | C | 1 | a0002c0001t0003g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1734+371T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442362 | |||||||
chr2:151442387 | T | TA | 4 | a0002c0001t0010g0209 a0002c0001t0010g0212 a0002c0001t0010g0232 others(1): Show |
4 | HG01081.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+396_1734+397i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442387 | |||||||
chr2:151442388 | T | A | 10 | a0001c0002t0001g0367 a0001c0003t0057g0262 a0002c0001t0010g0208 others(7): Show |
10 | HG00639.hp2 HG01081.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734+397T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442388 | |||||||
chr2:151442388 | TA | T | 32 | a0001c0002t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 others(29): Show |
32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1734+414delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442388 | ||||||
chr2:151442389 | A | T | 10 | a0002c0001t0008g0018 a0002c0001t0012g0044 a0002c0001t0026g0015 others(7): Show |
10 | HG00423.hp2 HG00609.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1734+398A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442389 | |||||||
chr2:151442390 | A | T | 1 | a0006c0011t0014g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1734+399A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442390 | |||||||
chr2:151442409 | A | T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1734+418A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442409 | |||||||
chr2:151442487 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+496A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442487 | |||||||
chr2:151442767 | A | AT | 106 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(103): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1735-468dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442767 | A | ATT | 17 | a0001c0002t0001g0307 a0001c0002t0001g0308 a0001c0002t0001g0326 others(14): Show |
17 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1735-469_1735-468d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442767 | ATTT | A | 9 | a0001c0003t0002g0108 a0001c0003t0002g0110 a0001c0003t0002g0119 others(6): Show |
9 | HG00741.hp2 HG02135.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1735-470_1735-468d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442767 | ATTTT | A | 76 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1735-471_1735-468d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442767 | ATTTTT | A | 32 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(29): Show |
32 | HG00639.hp1 HG01175.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1735-472_1735-468d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442767 | ATTTTTT | A | 7 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-473_1735-468d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | ||||||
chr2:151442813 | G | A | 19 | a0001c0002t0001g0001 a0001c0002t0001g0305 a0001c0002t0001g0307 others(16): Show |
20 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1735-446G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442813 | |||||||
chr2:151442841 | G | A | 81 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1735-418G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442841 | |||||||
chr2:151442933 | G | A | 1 | a0001c0004t0005g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1735-326G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442933 | |||||||
chr2:151443068 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1735-191G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443068 | |||||||
chr2:151443106 | AAAT | A | 36 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(33): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1735-149_1735-147d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151443106 | ||||||
chr2:151443113 | T | C | 1 | a0001c0009t0015g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1735-146T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443113 | |||||||
chr2:151443250 | C | T | 1 | a0002c0001t0066g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1735-9C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443250 | |||||||
chr2:151443470 | CATTAA | C | 17 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(14): Show |
17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1806-53_1806-49del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr2 | 151443470 | ||||||
chr2:151443747 | CCT | C | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986+39_1986+40del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443747 | |||||||
chr2:151443783 | A | G | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1986+74A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443783 | |||||||
chr2:151443870 | C | T | 1 | a0001c0003t0002g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1986+161C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443870 | |||||||
chr2:151444094 | T | G | 1 | a0001c0004t0005g0081 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1986+385T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444094 | |||||||
chr2:151444310 | G | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986+601G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444310 | |||||||
chr2:151444435 | A | G | 274 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(271): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1986+726A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444435 | |||||||
chr2:151444439 | G | T | 1 | a0002c0001t0039g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1986+730G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444439 | |||||||
chr2:151444659 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-679G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444659 | |||||||
chr2:151444690 | T | C | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1987-648T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444690 | |||||||
chr2:151444792 | A | T | 266 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1987-546A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444792 | |||||||
chr2:151445081 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-257A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151445081 | |||||||
chr2:151445121 | T | A | 1 | a0003c0005t0007g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1987-217T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151445121 | |||||||
chr2:151445607 | G | T | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2094+162G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445607 | |||||||
chr2:151445618 | G | T | 9 | a0001c0003t0002g0105 a0001c0003t0002g0106 a0001c0003t0002g0117 others(6): Show |
9 | HG00621.hp1 NA18947.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+173G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445618 | |||||||
chr2:151445619 | C | T | 9 | a0001c0003t0002g0105 a0001c0003t0002g0106 a0001c0003t0002g0117 others(6): Show |
9 | HG00621.hp1 NA18947.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+174C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445619 | |||||||
chr2:151445685 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+240T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445685 | |||||||
chr2:151445807 | G | A | 4 | a0003c0005t0016g0180 a0003c0005t0016g0181 a0003c0005t0016g0182 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+362G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445807 | |||||||
chr2:151445828 | T | C | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+383T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445828 | |||||||
chr2:151445860 | ACTT | A | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+419_2094+421d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | INFO_REALIGN_3_PRIME | chr2 | 151445860 | ||||||
chr2:151445941 | A | G | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-485A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445941 | |||||||
chr2:151446081 | A | T | 1 | a0006c0011t0014g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2095-345A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446081 | |||||||
chr2:151446111 | A | G | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2095-315A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446111 | |||||||
chr2:151446163 | C | T | 1 | a0001c0022t0025g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2095-263C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446163 | |||||||
chr2:151446205 | G | T | 1 | a0001c0004t0006g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2095-221G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446205 | |||||||
chr2:151446218 | C | T | 1 | a0001c0003t0002g0145 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2095-208C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446218 | |||||||
chr2:151446254 | C | T | 6 | a0001c0002t0001g0301 a0001c0002t0001g0306 a0001c0002t0001g0308 others(3): Show |
6 | HG00438.hp1 NA18952.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2095-172C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446254 | |||||||
chr2:151446296 | G | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-130G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446296 | |||||||
chr2:151446412 | G | C | 1 | a0001c0003t0002g0002 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2095-14G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446412 | |||||||
chr2:151446657 | G | A | 264 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2244+82G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446657 | |||||||
chr2:151446662 | C | G | 1 | a0002c0001t0004g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2244+87C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446662 | |||||||
chr2:151446761 | G | T | 4 | a0001c0004t0005g0062 a0001c0004t0005g0078 a0001c0004t0005g0079 others(1): Show |
4 | HG00673.hp1 HG02056.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+186G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446761 | |||||||
chr2:151446792 | T | C | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2244+217T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446792 | |||||||
chr2:151446945 | C | CT | 133 | a0001c0002t0025g0194 a0001c0002t0025g0195 a0001c0003t0002g0002 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.2244+386dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151446945 | ||||||
chr2:151446945 | CTTT | C | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2244+384_2244+386d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151446945 | ||||||
chr2:151446947 | T | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+372T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446947 | |||||||
chr2:151446949 | T | C | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2244+374T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446949 | |||||||
chr2:151446966 | C | T | 119 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.2244+391C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446966 | |||||||
chr2:151446982 | C | T | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2244+407C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446982 | |||||||
chr2:151447015 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+440C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447015 | |||||||
chr2:151447034 | C | T | 1 | a0001c0004t0006g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2244+459C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447034 | |||||||
chr2:151447037 | G | A | 103 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2244+462G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447037 | |||||||
chr2:151447293 | T | C | 6 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(3): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+718T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447293 | |||||||
chr2:151447295 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2244+720C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447295 | |||||||
chr2:151447333 | C | T | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2244+758C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447333 | |||||||
chr2:151447410 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+835A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447410 | |||||||
chr2:151447530 | T | C | 1 | a0001c0007t0023g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2244+955T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447530 | |||||||
chr2:151447598 | T | C | 1 | a0001c0003t0058g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2244+1023T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447598 | |||||||
chr2:151447638 | TG | T | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1066delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151447638 | ||||||
chr2:151447717 | G | C | 1 | a0001c0003t0027g0114 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2244+1142G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447717 | |||||||
chr2:151447736 | G | T | 4 | a0001c0003t0002g0120 a0001c0003t0002g0147 a0001c0003t0002g0151 others(1): Show |
4 | HG00609.hp2 HG02523.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1161G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447736 | |||||||
chr2:151447889 | A | G | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2244+1314A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447889 | |||||||
chr2:151448087 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1512A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448087 | |||||||
chr2:151448180 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1605A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448180 | |||||||
chr2:151448244 | G | A | 114 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.2244+1669G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448244 | |||||||
chr2:151448333 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2244+1758C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448333 | |||||||
chr2:151448336 | G | C | 1 | a0003c0005t0007g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2244+1761G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448336 | |||||||
chr2:151448568 | A | G | 1 | a0001c0004t0006g0075 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2244+1993A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448568 | |||||||
chr2:151448649 | T | C | 1 | a0001c0002t0045g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2244+2074T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448649 | |||||||
chr2:151448677 | G | GT | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+2103dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151448677 | ||||||
chr2:151448836 | T | A | 1 | a0001c0004t0005g0078 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2244+2261T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448836 | |||||||
chr2:151448922 | A | T | 1 | a0002c0001t0003g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2244+2347A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448922 | |||||||
chr2:151449292 | C | T | 1 | a0006c0011t0014g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2245-2314C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449292 | |||||||
chr2:151449396 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-2210A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449396 | |||||||
chr2:151449423 | CT | C | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-2176delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449423 | ||||||
chr2:151449439 | CTT | C | 3 | a0009c0014t0001g0377 a0009c0014t0001g0378 a0009c0014t0001g0379 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2245-2163_2245-216 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449439 | ||||||
chr2:151449461 | T | C | 2 | a0002c0001t0026g0042 a0002c0001t0026g0043 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2245-2145T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449461 | |||||||
chr2:151449521 | T | C | 262 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2245-2085T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449521 | |||||||
chr2:151449748 | A | AC | 162 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2245-1858_2245-185 others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449748 | |||||||
chr2:151449842 | GC | G | 31 | a0001c0004t0005g0052 a0001c0004t0005g0063 a0001c0004t0005g0064 others(28): Show |
31 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.2245-1762delC | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449842 | ||||||
chr2:151449843 | C | A | 3 | a0002c0001t0019g0006 a0002c0001t0019g0007 a0002c0001t0019g0008 |
3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2245-1763C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449843 | |||||||
chr2:151449844 | C | CT | 218 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2245-1747dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449844 | ||||||
chr2:151449844 | C | G | 6 | a0001c0004t0005g0062 a0001c0004t0005g0086 a0001c0004t0006g0054 others(3): Show |
6 | HG01358.hp2 HG02071.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.2245-1762C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449844 | |||||||
chr2:151449845 | T | G | 31 | a0001c0004t0005g0052 a0001c0004t0005g0063 a0001c0004t0005g0064 others(28): Show |
31 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.2245-1761T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449845 | |||||||
chr2:151449912 | G | A | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2245-1694G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449912 | |||||||
chr2:151449934 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2245-1672C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449934 | |||||||
chr2:151450157 | T | C | 22 | a0001c0003t0058g0261 a0003c0005t0007g0278 a0003c0005t0007g0279 others(19): Show |
22 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2245-1449T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450157 | |||||||
chr2:151450383 | T | G | 120 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2245-1223T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450383 | |||||||
chr2:151450451 | T | G | 1 | a0002c0001t0008g0038 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2245-1155T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450451 | |||||||
chr2:151450545 | T | C | 3 | a0001c0002t0001g0306 a0001c0002t0001g0372 a0001c0002t0051g0363 |
3 | HG00438.hp1 NA18952.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2245-1061T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450545 | |||||||
chr2:151450577 | C | A | 97 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(94): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2245-1029C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450577 | |||||||
chr2:151450594 | C | CT | 6 | a0001c0002t0001g0178 a0001c0002t0001g0333 a0001c0002t0001g0340 others(3): Show |
6 | HG01978.hp1 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1001dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151450594 | ||||||
chr2:151450609 | G | A | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2245-997G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450609 | |||||||
chr2:151450616 | C | G | 1 | a0001c0003t0059g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2245-990C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450616 | |||||||
chr2:151450662 | C | T | 1 | a0026c0031t0002g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2245-944C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450662 | |||||||
chr2:151450707 | C | T | 4 | a0001c0003t0002g0130 a0001c0003t0002g0132 a0001c0003t0002g0134 others(1): Show |
4 | HG01081.hp1 HG01255.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-899C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450707 | |||||||
chr2:151450709 | G | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2245-897G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450709 | |||||||
chr2:151450921 | G | A | 17 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(14): Show |
17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2245-685G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450921 | |||||||
chr2:151450979 | G | A | 2 | a0002c0001t0003g0187 a0002c0001t0003g0190 |
2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2245-627G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450979 | |||||||
chr2:151450981 | A | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-625A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450981 | |||||||
chr2:151451192 | C | T | 104 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(101): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2245-414C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451192 | |||||||
chr2:151451277 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2245-329C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451277 | |||||||
chr2:151451359 | A | T | 4 | a0001c0003t0024g0266 a0001c0003t0024g0267 a0001c0003t0024g0268 others(1): Show |
4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-247A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451359 | |||||||
chr2:151451364 | G | A | 1 | a0001c0002t0001g0362 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2245-242G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451364 | |||||||
chr2:151452097 | T | G | 120 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2344+392T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452097 | |||||||
chr2:151452196 | A | C | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2344+491A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452196 | |||||||
chr2:151452361 | T | C | 265 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2344+656T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452361 | |||||||
chr2:151452862 | A | G | 1 | a0001c0003t0002g0102 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2344+1157A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452862 | |||||||
chr2:151452871 | C | T | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344+1166C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452871 | |||||||
chr2:151453002 | G | A | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2344+1297G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453002 | |||||||
chr2:151453397 | C | T | 1 | a0002c0001t0067g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2345-1498C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453397 | |||||||
chr2:151453449 | C | T | 17 | a0001c0002t0001g0001 a0001c0002t0001g0305 a0001c0002t0001g0307 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2345-1446C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453449 | |||||||
chr2:151453579 | C | CA | 67 | a0001c0003t0002g0050 a0001c0003t0002g0111 a0001c0003t0002g0118 others(64): Show |
67 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2345-1293dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | ||||||
chr2:151453579 | C | CAA | 14 | a0001c0003t0002g0134 a0001c0003t0002g0139 a0001c0004t0005g0062 others(11): Show |
14 | HG01081.hp1 HG02145.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.2345-1294_2345-129 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | ||||||
chr2:151453579 | CA | C | 32 | a0001c0002t0001g0305 a0001c0002t0001g0311 a0001c0002t0001g0321 others(29): Show |
32 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2345-1293delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | ||||||
chr2:151453579 | CAA | C | 76 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(73): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2345-1294_2345-129 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | ||||||
chr2:151453609 | T | A | 21 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(18): Show |
21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2345-1286T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453609 | |||||||
chr2:151453613 | C | T | 1 | a0001c0003t0002g0143 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2345-1282C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453613 | |||||||
chr2:151453741 | G | A | 1 | a0002c0001t0039g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2345-1154G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453741 | |||||||
chr2:151454351 | A | T | 1 | a0002c0001t0003g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2345-544A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454351 | |||||||
chr2:151454381 | G | A | 1 | a0002c0001t0066g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2345-514G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454381 | |||||||
chr2:151454414 | T | G | 119 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.2345-481T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454414 | |||||||
chr2:151454472 | C | G | 2 | a0002c0001t0004g0014 a0002c0001t0004g0021 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2345-423C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454472 | |||||||
chr2:151454736 | T | C | 1 | a0002c0001t0003g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2345-159T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454736 | |||||||
chr2:151455173 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609+14A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455173 | |||||||
chr2:151455175 | T | A | 2 | a0001c0003t0057g0262 a0001c0003t0058g0261 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2609+16T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455175 | |||||||
chr2:151455563 | C | A | 42 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(39): Show |
42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2609+404C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455563 | |||||||
chr2:151455566 | T | C | 1 | a0002c0001t0039g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2609+407T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455566 | |||||||
chr2:151455661 | CAT | C | 118 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.2609+505_2609+506d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr2 | 151455661 | ||||||
chr2:151455783 | C | T | 1 | a0001c0003t0028g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2609+624C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455783 | |||||||
chr2:151455819 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609+660C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455819 | |||||||
chr2:151456062 | C | T | 1 | a0002c0001t0003g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2610-516C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456062 | |||||||
chr2:151456237 | G | A | 1 | a0002c0001t0017g0199 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2610-341G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456237 | |||||||
chr2:151456428 | G | GT | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2610-144dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr2 | 151456428 | ||||||
chr2:151456548 | A | C | 1 | a0002c0001t0004g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2610-30A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456548 | |||||||
chr2:151456802 | G | A | 36 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(33): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2652+182G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456802 | |||||||
chr2:151456925 | G | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2652+305G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456925 | |||||||
chr2:151456953 | C | T | 16 | a0002c0001t0004g0036 a0002c0001t0004g0037 a0002c0001t0004g0039 others(13): Show |
16 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.2652+333C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456953 | |||||||
chr2:151456971 | T | G | 1 | a0007c0012t0007g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2652+351T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456971 | |||||||
chr2:151456975 | T | C | 265 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2652+355T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456975 | |||||||
chr2:151457025 | C | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2652+405C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457025 | |||||||
chr2:151457049 | A | T | 1 | a0001c0004t0041g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2652+429A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457049 | |||||||
chr2:151457084 | A | G | 1 | a0002c0001t0003g0222 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2652+464A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457084 | |||||||
chr2:151457087 | G | GT | 31 | a0001c0002t0001g0337 a0001c0004t0006g0057 a0001c0007t0022g0264 others(28): Show |
31 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.2652+480dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr2 | 151457087 | ||||||
chr2:151457087 | G | T | 1 | a0001c0003t0024g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2652+467G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457087 | |||||||
chr2:151457136 | A | G | 3 | a0002c0001t0012g0066 a0002c0001t0012g0068 a0002c0001t0012g0069 |
3 | NA18968.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2652+516A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457136 | |||||||
chr2:151457205 | C | G | 1 | a0001c0003t0056g0309 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2653-556C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457205 | |||||||
chr2:151457223 | G | A | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2653-538G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457223 | |||||||
chr2:151457234 | C | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2653-527C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457234 | |||||||
chr2:151457312 | G | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2653-449G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457312 | |||||||
chr2:151457499 | G | A | 1 | a0007c0012t0007g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2653-262G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457499 | |||||||
chr2:151457583 | TTAA | T | 21 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(18): Show |
21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2653-174_2653-172d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr2 | 151457583 | ||||||
chr2:151457585 | A | G | 2 | a0004c0006t0009g0165 a0004c0006t0009g0170 |
2 | NA18983.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2653-176A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457585 | |||||||
chr2:151457658 | G | T | 5 | a0001c0004t0005g0086 a0001c0004t0005g0087 a0001c0004t0005g0089 others(2): Show |
5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2653-103G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457658 | |||||||
chr2:151458033 | C | CA | 265 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2855+73dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458033 | ||||||
chr2:151458160 | C | T | 1 | a0018c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2855+197C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458160 | |||||||
chr2:151458225 | G | GT | 3 | a0003c0005t0007g0288 a0007c0012t0007g0289 a0022c0027t0016g0282 |
3 | HG02257.hp2 HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2855+262_2855+263i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458225 | |||||||
chr2:151458226 | A | AT | 158 | a0001c0002t0001g0001 a0001c0002t0001g0298 a0001c0002t0001g0303 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.2855+287dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | ||||||
chr2:151458226 | A | ATT | 29 | a0001c0002t0001g0178 a0001c0002t0001g0297 a0001c0002t0001g0300 others(26): Show |
29 | HG00423.hp1 HG00558.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.2855+286_2855+287d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | ||||||
chr2:151458226 | A | ATTT | 6 | a0001c0002t0001g0349 a0001c0002t0045g0302 a0001c0002t0048g0185 others(3): Show |
6 | HG00621.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2855+285_2855+287d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | ||||||
chr2:151458226 | A | T | 19 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(16): Show |
19 | HG01175.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2855+263A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458226 | |||||||
chr2:151458226 | AT | A | 8 | a0001c0002t0025g0194 a0001c0038t0030g0265 a0002c0001t0003g0179 others(5): Show |
8 | HG01515.hp2 HG01891.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.2855+287delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | ||||||
chr2:151458226 | ATTTTTTT others(5): Show |
A | 1 | a0002c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2855+276_2855+287d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | ||||||
chr2:151458284 | G | A | 1 | a0001c0002t0045g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2855+321G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458284 | |||||||
chr2:151458325 | C | T | 2 | a0005c0018t0031g0248 a0005c0018t0031g0249 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2855+362C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458325 | |||||||
chr2:151458397 | T | A | 83 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2856-414T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458397 | |||||||
chr2:151458540 | T | A | 1 | a0001c0002t0045g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2856-271T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458540 | |||||||
chr2:151458595 | C | T | 1 | a0001c0002t0001g0359 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2856-216C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458595 | |||||||
chr2:151458753 | A | G | 10 | a0002c0001t0003g0196 a0002c0001t0003g0203 a0002c0001t0003g0216 others(7): Show |
10 | HG00438.hp2 HG02080.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.2856-58A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458753 | |||||||
chr2:151458762 | C | T | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2856-49C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458762 | |||||||
chr2:151458923 | G | A | 1 | a0028c0037t0021g0334 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2955+13G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151458923 | |||||||
chr2:151458980 | G | A | 6 | a0001c0003t0002g0002 a0001c0003t0002g0110 a0001c0003t0002g0137 others(3): Show |
6 | HG01993.hp1 HG02004.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2955+70G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151458980 | |||||||
chr2:151459035 | G | T | 264 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2955+125G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459035 | |||||||
chr2:151459211 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+301A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459211 | |||||||
chr2:151459302 | G | C | 266 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2955+392G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459302 | |||||||
chr2:151459302 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+392G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459302 | |||||||
chr2:151459418 | T | C | 1 | a0002c0001t0065g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2955+508T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459418 | |||||||
chr2:151459440 | A | G | 3 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 |
3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2955+530A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459440 | |||||||
chr2:151459554 | G | T | 42 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(39): Show |
42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2956-446G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459554 | |||||||
chr2:151459588 | A | G | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2956-412A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459588 | |||||||
chr2:151459590 | A | G | 1 | a0001c0002t0001g0366 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2956-410A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459590 | |||||||
chr2:151459604 | G | A | 1 | a0002c0001t0003g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2956-396G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459604 | |||||||
chr2:151459613 | C | T | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2956-387C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459613 | |||||||
chr2:151459624 | A | G | 1 | a0001c0002t0001g0351 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2956-376A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459624 | |||||||
chr2:151459642 | G | C | 1 | a0002c0001t0003g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2956-358G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459642 | |||||||
chr2:151459830 | G | A | 42 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(39): Show |
42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2956-170G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459830 | |||||||
chr2:151460154 | A | T | 1 | a0001c0003t0035g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3075+35A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460154 | |||||||
chr2:151460159 | G | T | 1 | a0021c0029t0030g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3075+40G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460159 | |||||||
chr2:151460226 | G | A | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3075+107G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460226 | |||||||
chr2:151460526 | TCTTATCA others(2): Show |
T | 265 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.3075+408_3075+416d others(11): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460526 | |||||||
chr2:151460527 | C | T | 1 | a0002c0001t0010g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3075+408C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460527 | |||||||
chr2:151460536 | T | A | 265 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.3075+417T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460536 | |||||||
chr2:151460637 | GTGAAA | G | 3 | a0001c0007t0023g0263 a0001c0007t0023g0270 a0001c0007t0023g0271 |
3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3076-495_3076-491d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr2 | 151460637 | ||||||
chr2:151460789 | C | T | 1 | a0001c0004t0006g0073 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3076-349C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460789 | |||||||
chr2:151460881 | G | A | 38 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(35): Show |
38 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.3076-257G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460881 | |||||||
chr2:151460924 | C | G | 1 | a0008c0008t0001g0338 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3076-214C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460924 | |||||||
chr2:151461007 | G | A | 1 | a0002c0001t0003g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3076-131G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461007 | |||||||
chr2:151461017 | T | C | 121 | a0001c0002t0001g0297 a0001c0003t0002g0002 a0001c0003t0002g0049 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.3076-121T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461017 | |||||||
chr2:151461074 | T | C | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3076-64T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461074 | |||||||
chr2:151461391 | A | AT | 48 | a0001c0002t0001g0307 a0001c0002t0001g0330 a0001c0002t0001g0333 others(45): Show |
48 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.3227+120dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr2 | 151461391 | ||||||
chr2:151461461 | G | A | 1 | a0027c0030t0006g0072 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3227+172G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461461 | |||||||
chr2:151461483 | C | A | 1 | a0001c0003t0002g0174 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3227+194C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461483 | |||||||
chr2:151461517 | G | A | 86 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.3227+228G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461517 | |||||||
chr2:151461814 | C | T | 1 | a0001c0009t0015g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3228-428C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461814 | |||||||
chr2:151461917 | A | G | 1 | a0001c0003t0027g0115 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3228-325A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461917 | |||||||
chr2:151461986 | G | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.3228-256G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461986 | |||||||
chr2:151461999 | A | T | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3228-243A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461999 | |||||||
chr2:151462084 | G | A | 36 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(33): Show |
36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.3228-158G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151462084 | |||||||
chr2:151462169 | G | T | 2 | a0001c0002t0001g0344 a0014c0021t0001g0345 |
2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.3228-73G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151462169 | |||||||
chr2:151462199 | TATC | T | 103 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.3228-39_3228-37del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr2 | 151462199 | ||||||
chr2:151462334 | A | G | 7 | a0001c0003t0011g0116 a0001c0003t0011g0135 a0001c0003t0011g0150 others(4): Show |
7 | NA18940.hp2 NA18957.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.3308+12A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/35 | chr2 | 151462334 | |||||||
chr2:151462399 | A | G | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3309-13A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/35 | chr2 | 151462399 | |||||||
chr2:151462471 | G | A | 6 | a0001c0002t0001g0326 a0001c0002t0001g0370 a0001c0002t0021g0324 others(3): Show |
6 | NA18987.hp2 NA18990.hp2 NA19003.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3363+5G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | chr2 | 151462471 | |||||||
chr2:151462648 | A | AGT | 190 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(187): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.3363+201_3363+202d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151462648 | A | AGTGT | 8 | a0001c0002t0001g0364 a0001c0003t0002g0129 a0001c0004t0006g0076 others(5): Show |
8 | HG00099.hp2 HG00544.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.3363+199_3363+202d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151462648 | A | AGTGTGT | 7 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0018t0031g0248 others(4): Show |
7 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363+197_3363+202d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151462648 | A | AGTGTGTG others(3): Show |
2 | a0005c0010t0018g0246 a0005c0010t0018g0247 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3363+193_3363+202d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151462648 | AGTGT | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363+199_3363+202d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151462648 | AGTGTGT | A | 3 | a0002c0001t0003g0204 a0002c0001t0003g0205 a0002c0001t0003g0206 |
3 | HG00544.hp1 NA18951.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3363+197_3363+202d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | ||||||
chr2:151466516 | G | A | 1 | a0001c0004t0005g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6600+396G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466516 | |||||||
chr2:151466572 | C | A | 103 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6600+452C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466572 | |||||||
chr2:151466724 | TAAAA | T | 5 | a0001c0007t0023g0263 a0001c0009t0015g0250 a0001c0009t0015g0251 others(2): Show |
5 | HG02809.hp1 HG03491.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.6600+608_6600+611d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr2 | 151466724 | ||||||
chr2:151466785 | T | C | 14 | a0001c0002t0001g0001 a0001c0002t0001g0307 a0001c0002t0001g0314 others(11): Show |
15 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.6600+665T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466785 | |||||||
chr2:151466833 | G | T | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6600+713G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466833 | |||||||
chr2:151466992 | C | A | 4 | a0001c0004t0005g0062 a0001c0004t0005g0078 a0001c0004t0005g0079 others(1): Show |
4 | HG00673.hp1 HG02056.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.6600+872C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466992 | |||||||
chr2:151467018 | C | G | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6600+898C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467018 | |||||||
chr2:151467039 | A | G | 83 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.6600+919A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467039 | |||||||
chr2:151467099 | C | T | 1 | a0001c0002t0001g0333 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6601-901C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467099 | |||||||
chr2:151467113 | C | A | 4 | a0001c0009t0015g0250 a0001c0009t0015g0251 a0001c0009t0015g0252 others(1): Show |
4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.6601-887C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467113 | |||||||
chr2:151467132 | G | C | 6 | a0005c0010t0018g0183 a0005c0010t0018g0184 a0005c0010t0018g0246 others(3): Show |
6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.6601-868G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467132 | |||||||
chr2:151467171 | G | C | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.6601-829G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467171 | |||||||
chr2:151467206 | C | T | 90 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.6601-794C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467206 | |||||||
chr2:151467214 | C | T | 1 | a0001c0038t0030g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6601-786C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467214 | |||||||
chr2:151467306 | C | A | 22 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(19): Show |
22 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.6601-694C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467306 | |||||||
chr2:151467385 | A | G | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6601-615A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467385 | |||||||
chr2:151467624 | C | T | 1 | a0002c0001t0003g0207 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6601-376C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467624 | |||||||
chr2:151467674 | G | A | 21 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 others(18): Show |
21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.6601-326G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467674 | |||||||
chr2:151467695 | C | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.6601-305C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467695 | |||||||
chr2:151468221 | G | C | 1 | a0001c0003t0024g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6747+75G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 31/35 | chr2 | 151468221 | |||||||
chr2:151468275 | G | C | 263 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.6747+129G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 31/35 | chr2 | 151468275 | |||||||
chr2:151468574 | T | C | 1 | a0002c0001t0004g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.6825+23T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 32/35 | chr2 | 151468574 | |||||||
chr2:151468774 | C | T | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.6941+18C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151468774 | |||||||
chr2:151468833 | C | T | 1 | a0001c0004t0006g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6941+77C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151468833 | |||||||
chr2:151469057 | G | A | 2 | a0001c0002t0025g0194 a0001c0002t0025g0195 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6941+301G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469057 | |||||||
chr2:151469125 | C | CA | 6 | a0002c0001t0012g0044 a0002c0001t0012g0045 a0002c0001t0012g0066 others(3): Show |
6 | HG00323.hp1 HG02683.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.6941+370dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr2 | 151469125 | ||||||
chr2:151469168 | A | G | 3 | a0003c0005t0016g0180 a0003c0005t0016g0181 a0003c0005t0016g0182 |
3 | HG02258.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.6941+412A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469168 | |||||||
chr2:151469229 | C | T | 1 | a0001c0003t0011g0155 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.6941+473C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469229 | |||||||
chr2:151469442 | G | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.6942-269G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469442 | |||||||
chr2:151469519 | C | T | 1 | a0001c0003t0002g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6942-192C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469519 | |||||||
chr2:151469576 | C | T | 1 | a0002c0001t0020g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6942-135C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469576 | |||||||
chr2:151470182 | C | A | 2 | a0003c0005t0007g0284 a0003c0005t0007g0285 |
2 | HG00639.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.7095+318C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470182 | |||||||
chr2:151470213 | C | CT | 87 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.7095+354dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151470213 | ||||||
chr2:151470214 | T | C | 1 | a0001c0004t0006g0075 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7095+350T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470214 | |||||||
chr2:151470408 | G | A | 3 | a0003c0005t0007g0281 a0003c0005t0007g0286 a0003c0019t0068g0287 |
3 | HG02965.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7095+544G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470408 | |||||||
chr2:151470456 | T | C | 2 | a0001c0002t0001g0370 a0001c0002t0050g0327 |
2 | NA18987.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.7095+592T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470456 | |||||||
chr2:151470638 | T | C | 1 | a0001c0002t0001g0314 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.7095+774T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470638 | |||||||
chr2:151470961 | G | T | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.7095+1097G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470961 | |||||||
chr2:151470979 | T | G | 1 | a0002c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7095+1115T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470979 | |||||||
chr2:151471025 | CT | C | 7 | a0002c0001t0019g0006 a0002c0001t0019g0007 a0002c0001t0019g0008 others(4): Show |
7 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.7095+1170delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151471025 | ||||||
chr2:151471236 | G | A | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7095+1372G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471236 | |||||||
chr2:151471387 | G | A | 2 | a0011c0015t0029g0004 a0011c0015t0029g0005 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.7095+1523G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471387 | |||||||
chr2:151471551 | G | A | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7095+1687G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471551 | |||||||
chr2:151471660 | G | T | 1 | a0002c0001t0008g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7095+1796G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471660 | |||||||
chr2:151471668 | C | T | 334 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(331): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.7095+1804C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471668 | |||||||
chr2:151471832 | C | A | 4 | a0006c0011t0014g0092 a0006c0011t0014g0093 a0006c0011t0014g0176 others(1): Show |
4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.7095+1968C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471832 | |||||||
chr2:151471853 | G | T | 1 | a0001c0002t0048g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7095+1989G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471853 | |||||||
chr2:151471945 | A | G | 1 | a0013c0026t0040g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7096-2019A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471945 | |||||||
chr2:151471979 | A | C | 1 | a0002c0001t0004g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7096-1985A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471979 | |||||||
chr2:151472065 | C | T | 1 | a0002c0001t0004g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7096-1899C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472065 | |||||||
chr2:151472067 | C | A | 1 | a0002c0001t0004g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7096-1897C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472067 | |||||||
chr2:151472067 | C | T | 1 | a0017c0034t0063g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7096-1897C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472067 | |||||||
chr2:151472085 | C | T | 1 | a0001c0002t0048g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7096-1879C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472085 | |||||||
chr2:151472086 | G | A | 2 | a0002c0001t0004g0014 a0002c0001t0004g0021 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7096-1878G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472086 | |||||||
chr2:151472235 | T | A | 3 | a0002c0001t0012g0044 a0002c0001t0012g0045 a0002c0001t0060g0373 |
3 | HG00323.hp1 HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.7096-1729T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472235 | |||||||
chr2:151472279 | A | G | 2 | a0001c0003t0011g0150 a0001c0003t0011g0155 |
2 | NA18940.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.7096-1685A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472279 | |||||||
chr2:151472431 | G | C | 1 | a0001c0004t0006g0057 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7096-1533G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472431 | |||||||
chr2:151472469 | T | C | 3 | a0001c0002t0025g0194 a0001c0002t0025g0195 a0001c0022t0025g0193 |
3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7096-1495T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472469 | |||||||
chr2:151472507 | T | G | 3 | a0003c0005t0007g0278 a0003c0005t0007g0279 a0003c0005t0007g0280 |
3 | HG02145.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.7096-1457T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472507 | |||||||
chr2:151472698 | G | A | 112 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.7096-1266G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472698 | |||||||
chr2:151472771 | G | C | 3 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 |
3 | HG02965.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.7096-1193G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472771 | |||||||
chr2:151472801 | A | G | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7096-1163A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472801 | |||||||
chr2:151472827 | A | T | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.7096-1137A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472827 | |||||||
chr2:151472936 | A | C | 3 | a0001c0002t0001g0310 a0001c0002t0001g0356 a0001c0002t0013g0091 |
3 | HG03834.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.7096-1028A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472936 | |||||||
chr2:151472990 | T | C | 1 | a0001c0003t0035g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.7096-974T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472990 | |||||||
chr2:151473003 | G | C | 5 | a0001c0004t0005g0086 a0001c0004t0005g0087 a0001c0004t0005g0089 others(2): Show |
5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.7096-961G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473003 | |||||||
chr2:151473006 | T | A | 2 | a0001c0002t0001g0322 a0001c0002t0001g0328 |
2 | HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7096-958T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473006 | |||||||
chr2:151473292 | C | CT | 9 | a0002c0001t0003g0187 a0002c0001t0003g0190 a0002c0001t0004g0012 others(6): Show |
9 | HG00639.hp2 HG02280.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.7096-650dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | ||||||
chr2:151473292 | CT | C | 119 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.7096-650delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | ||||||
chr2:151473292 | CTT | C | 39 | a0001c0002t0001g0375 a0001c0002t0021g0350 a0001c0002t0051g0363 others(36): Show |
39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.7096-651_7096-650d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | ||||||
chr2:151473292 | CTTT | C | 8 | a0001c0004t0005g0087 a0001c0004t0005g0089 a0001c0004t0005g0090 others(5): Show |
8 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.7096-652_7096-650d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | ||||||
chr2:151473340 | C | A | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7096-624C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473340 | |||||||
chr2:151473574 | C | T | 1 | a0001c0004t0005g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.7096-390C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473574 | |||||||
chr2:151473634 | A | G | 103 | a0001c0002t0001g0001 a0001c0002t0001g0178 a0001c0002t0001g0297 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.7096-330A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473634 | |||||||
chr2:151473644 | T | C | 1 | a0012c0024t0049g0336 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7096-320T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473644 | |||||||
chr2:151473759 | C | G | 3 | a0002c0001t0010g0208 a0002c0001t0010g0209 a0002c0001t0010g0234 |
3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.7096-205C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473759 | |||||||
chr2:151474133 | T | C | 6 | a0001c0007t0022g0264 a0001c0007t0022g0274 a0001c0007t0022g0275 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7204+61T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474133 | |||||||
chr2:151474346 | T | G | 1 | a0001c0022t0025g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7204+274T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474346 | |||||||
chr2:151474452 | G | A | 37 | a0001c0004t0005g0052 a0001c0004t0005g0062 a0001c0004t0005g0063 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.7204+380G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474452 | |||||||
chr2:151474458 | C | T | 1 | a0001c0002t0013g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7204+386C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474458 | |||||||
chr2:151474619 | T | C | 119 | a0001c0003t0002g0002 a0001c0003t0002g0049 a0001c0003t0002g0050 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.7205-238T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474619 |