Item | Value |
---|---|
geneid | 203054 |
ensemblid | ENSG00000173137.12 |
hgncid | 21738 |
symbol | ADCK5 |
name | aarF domain containing kinase 5 |
refseq_nuc | NM_174922.5 |
refseq_prot | NP_777582.4 |
ensembl_nuc | ENST00000308860.11 |
ensembl_prot | ENSP00000310547.6 |
mane_status | MANE Select |
chr | chr8 |
start | 144374047 |
end | 144393242 |
strand | + |
ver | v1.2 |
region | chr8:144374047-144393242 |
region5000 | chr8:144369047-144398242 |
regionname0 | ADCK5_chr8_144374047_144393242 |
regionname5000 | ADCK5_chr8_144369047_144398242 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 580 | 208 | 78 | 37 | 62 | 4 | 26 | 44 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(575): Show |
chr8 | 144369047 | 144398242 |
a0002 | 0/1 | 585 | 121 | 13 | 25 | 58 | 11 | 13 | 36 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(580): Show |
chr8 | 144369047 | 144398242 |
a0003 | 0/0 | 580 | 5 | 2 | 0 | 2 | 0 | 1 | 2 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(575): Show |
chr8 | 144369047 | 144398242 |
a0004 | 0/0 | 585 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(580): Show |
chr8 | 144369047 | 144398242 |
a0005 | 0/0 | 580 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(575): Show |
chr8 | 144369047 | 144398242 |
a0006 | 0/0 | 510 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(505): Show |
chr8 | 144369047 | 144398242 |
a0007 | 0/0 | 234 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(229): Show |
chr8 | 144369047 | 144398242 |
a0008 | 0/0 | 580 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(575): Show |
chr8 | 144369047 | 144398242 |
a0009 | 0/0 | 580 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(575): Show |
chr8 | 144369047 | 144398242 |
a0010 | 0/0 | 585 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | MWRPV others(580): Show |
chr8 | 144369047 | 144398242 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1740 | 156 | 35 | 31 | 62 | 3 | 24 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0001c0003 | 0/0 | 1740 | 50 | 42 | 5 | 0 | 1 | 2 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0001c0010 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0001c0012 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0002c0002 | 0/1 | 1755 | 120 | 13 | 25 | 57 | 11 | 13 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1750): Show |
chr8 | 144369047 | 144398242 | ||
a0002c0009 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1750): Show |
chr8 | 144369047 | 144398242 | ||
a0003c0004 | 0/0 | 1740 | 5 | 2 | 0 | 2 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0004c0005 | 0/0 | 1755 | 4 | 0 | 0 | 4 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1750): Show |
chr8 | 144369047 | 144398242 | ||
a0005c0006 | 0/0 | 1740 | 3 | 0 | 0 | 3 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0006c0008 | 0/0 | 1756 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1751): Show |
chr8 | 144369047 | 144398242 | ||
a0007c0011 | 0/0 | 1729 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1724): Show |
chr8 | 144369047 | 144398242 | ||
a0008c0014 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0009c0013 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1735): Show |
chr8 | 144369047 | 144398242 | ||
a0010c0007 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | ATGTG others(1750): Show |
chr8 | 144369047 | 144398242 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1960 | 17 | 14 | 2 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0001t0002 | 0/0 | 1960 | 132 | 16 | 29 | 61 | 3 | 23 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0001t0003 | 0/0 | 1960 | 3 | 3 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0001t0004 | 0/0 | 1960 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0001t0005 | 0/0 | 1960 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0001t0008 | 0/0 | 1960 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0003t0001 | 0/0 | 1960 | 49 | 41 | 5 | 0 | 1 | 2 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0003t0006 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0010t0001 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0001c0012t0002 | 0/0 | 1960 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0002c0002t0001 | 0/1 | 1975 | 119 | 13 | 25 | 56 | 11 | 13 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1970): Show |
chr8 | 144369047 | 144398242 |
a0002c0002t0007 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1970): Show |
chr8 | 144369047 | 144398242 |
a0002c0009t0001 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1970): Show |
chr8 | 144369047 | 144398242 |
a0003c0004t0001 | 0/0 | 1960 | 3 | 2 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0003c0004t0002 | 0/0 | 1960 | 2 | 0 | 0 | 2 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0004c0005t0001 | 0/0 | 1975 | 4 | 0 | 0 | 4 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1970): Show |
chr8 | 144369047 | 144398242 |
a0005c0006t0002 | 0/0 | 1960 | 3 | 0 | 0 | 3 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0006c0008t0001 | 0/0 | 1976 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1971): Show |
chr8 | 144369047 | 144398242 |
a0007c0011t0002 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1944): Show |
chr8 | 144369047 | 144398242 |
a0008c0014t0002 | 0/0 | 1960 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0009c0013t0002 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1955): Show |
chr8 | 144369047 | 144398242 |
a0010c0007t0001 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | GAGAC others(1970): Show |
chr8 | 144369047 | 144398242 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0001 | 0/0 | 38 | 0 | 5 | 26 | 0 | 7 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0008 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0014 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0003t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0001c0012t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0002 | 0/0 | 25 | 3 | 6 | 11 | 2 | 3 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 2 | 0 | 4 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0005 | 0/0 | 6 | 1 | 3 | 0 | 2 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0022 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0132 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0002t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0002c0009t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0003c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0003c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0003c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0004c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0004c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0004c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0004c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0005c0006t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0005c0006t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0005c0006t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0006c0008t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0007c0011t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0008c0014t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0009c0013t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
a0010c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0125 | EUR | GBR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | FIN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0128 | EUR | FIN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | FIN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01081 | hp1 | a0001 | c0012 | t0002 | g0001 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01255 | hp2 | a0006 | c0008 | t0001 | g0055 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01516 | hp2 | a0007 | c0011 | t0002 | g0158 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG01993 | hp2 | a0008 | c0014 | t0002 | g0001 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02015 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02071 | hp1 | a0002 | c0002 | t0007 | g0002 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02155 | hp2 | a0002 | c0009 | t0001 | g0018 | EAS | CDX | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | CDX | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CDX | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02280 | hp1 | a0001 | c0003 | t0006 | g0038 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0078 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02922 | hp2 | a0009 | c0013 | t0002 | g0186 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0054 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | ESN | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | STU | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CHB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18944 | hp2 | a0003 | c0004 | t0002 | g0104 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18951 | hp2 | a0010 | c0007 | t0001 | g0106 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18975 | hp2 | a0004 | c0005 | t0001 | g0119 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18983 | hp2 | a0004 | c0005 | t0001 | g0113 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18984 | hp2 | a0005 | c0006 | t0002 | g0169 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18997 | hp2 | a0004 | c0005 | t0001 | g0116 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19003 | hp1 | a0005 | c0006 | t0002 | g0174 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19004 | hp2 | a0003 | c0004 | t0002 | g0086 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | LWK | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19087 | hp2 | a0004 | c0005 | t0001 | g0118 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19089 | hp1 | a0005 | c0006 | t0002 | g0142 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ASW | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ASW | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | TSI | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | GIH | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20905 | hp2 | a0003 | c0004 | t0001 | g0122 | SAS | GIH | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02109 | hp2 | a0001 | c0010 | t0001 | g0040 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | USA | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | USA | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | USA | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | USA | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | LWK | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0132 | REF | REF | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0046 | REF | REF | ADCK5_chr8_144369047_144398242 | ADCK5 | chr8 | 144369047 | 144398242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:144379425 | C | A | 5 | a0002 a0003 a0004 others(2): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
missense_variant | MODERATE | c.51C>A | p.Ser17Arg | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/15 | 100/1960 | 51/1743 | 17/580 | chr8 | 144379425 | |||
chr8:144391006 | C | T | 1 | a0008 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.493C>T | p.Arg165Trp | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 5/15 | 542/1960 | 493/1743 | 165/580 | chr8 | 144391006 | |||
chr8:144391018 | G | A | 1 | a0005 | 3 | NA18984.hp2 NA19003.hp1 NA19089.hp1 |
missense_variant | MODERATE | c.505G>A | p.Val169Met | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 5/15 | 554/1960 | 505/1743 | 169/580 | chr8 | 144391018 | |||
chr8:144391042 | C | T | 1 | a0009 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.529C>T | p.Arg177Trp | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 5/15 | 578/1960 | 529/1743 | 177/580 | chr8 | 144391042 | |||
chr8:144391183 | TCCAGGAG others(4): Show |
T | 1 | a0007 | 1 | HG01516.hp2 | frameshift_variant | HIGH | c.594_604delCCAGGAGT others(3): Show |
p.Phe198fs | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/15 | 643/1960 | 594/1743 | 198/580 | chr8 | 144391183 | |||
chr8:144391823 | A | G | 1 | a0004 | 4 | NA18975.hp2 NA18983.hp2 NA18997.hp2 others(1): Show |
missense_variant | MODERATE | c.971A>G | p.Asn324Ser | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 9/15 | 1020/1960 | 971/1743 | 324/580 | chr8 | 144391823 | |||
chr8:144391993 | T | A | 1 | a0010 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1067T>A | p.Phe356Tyr | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 10/15 | 1116/1960 | 1067/1743 | 356/580 | chr8 | 144391993 | |||
chr8:144392145 | G | A | 1 | a0010 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1150G>A | p.Gly384Arg | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 11/15 | 1199/1960 | 1150/1743 | 384/580 | chr8 | 144392145 | |||
chr8:144392257 | C | A | 1 | a0010 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1179C>A | p.Asp393Glu | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/15 | 1228/1960 | 1179/1743 | 393/580 | chr8 | 144392257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:144390695 | C | A | 1 | a0001c0010 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.291C>A | p.Ile97Ile | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 4/15 | 340/1960 | 291/1743 | 97/580 | chr8 | 144390695 | |||
chr8:144390927 | C | T | 1 | a0002c0009 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.414C>T | p.Ala138Ala | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 5/15 | 463/1960 | 414/1743 | 138/580 | chr8 | 144390927 | |||
chr8:144392123 | G | A | 1 | a0001c0012 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.1128G>A | p.Ala376Ala | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 11/15 | 1177/1960 | 1128/1743 | 376/580 | chr8 | 144392123 | |||
chr8:144392695 | A | G | 1 | a0001c0003 | 50 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(47): Show |
splice_region_variant&synonymous_variant | LOW | c.1518A>G | p.Lys506Lys | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 13/15 | 1567/1960 | 1518/1743 | 506/580 | chr8 | 144392695 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:144374091 | C | T | 1 | a0001c0001t0003 | 3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-5C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/15 | chr8 | 144374091 | |||||||
chr8:144393083 | C | T | 1 | a0001c0001t0008 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 9 | chr8 | 144393083 | ||||||
chr8:144393094 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(7): Show |
145 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*20G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 20 | chr8 | 144393094 | ||||||
chr8:144393097 | G | A | 9 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(6): Show |
143 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 23 | chr8 | 144393097 | ||||||
chr8:144393114 | G | C | 1 | a0001c0003t0006 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 40 | chr8 | 144393114 | ||||||
chr8:144393141 | G | A | 1 | a0001c0001t0005 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*67G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 67 | chr8 | 144393141 | ||||||
chr8:144393157 | C | T | 1 | a0002c0002t0007 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 15/15 | 83 | chr8 | 144393157 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:144374681 | C | A | 1 | a0001c0003t0006g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+574C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374681 | |||||||
chr8:144374739 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.12+632G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374739 | |||||||
chr8:144374741 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.12+634C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374741 | |||||||
chr8:144374771 | T | TGCGTCGT others(17): Show |
1 | a0002c0002t0001g0199 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.12+665_12+688dupGC others(22): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 144374771 | ||||||
chr8:144374773 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+666C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374773 | |||||||
chr8:144374855 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.12+748C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374855 | |||||||
chr8:144374872 | T | C | 1 | a0001c0010t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12+765T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374872 | |||||||
chr8:144374909 | C | T | 1 | a0001c0001t0003g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.12+802C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144374909 | |||||||
chr8:144375095 | T | C | 9 | a0001c0003t0001g0007 a0001c0003t0001g0016 a0001c0003t0001g0017 others(6): Show |
17 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.12+988T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375095 | |||||||
chr8:144375229 | TGGCCAGT others(6): Show |
T | 1 | a0001c0010t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12+1126_12+1138del others(13): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 144375229 | ||||||
chr8:144375268 | A | G | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.12+1161A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375268 | |||||||
chr8:144375325 | C | T | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.12+1218C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375325 | |||||||
chr8:144375335 | T | C | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.12+1228T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375335 | |||||||
chr8:144375416 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.12+1309A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375416 | |||||||
chr8:144375608 | C | A | 1 | a0001c0003t0001g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.12+1501C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375608 | |||||||
chr8:144375707 | C | T | 3 | a0002c0002t0001g0191 a0002c0002t0001g0192 a0002c0002t0001g0193 |
3 | HG00738.hp2 HG01928.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.12+1600C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375707 | |||||||
chr8:144375777 | G | C | 84 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0002g0001 others(81): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.12+1670G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375777 | |||||||
chr8:144375778 | G | C | 1 | a0001c0001t0002g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.12+1671G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375778 | |||||||
chr8:144375869 | T | G | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.12+1762T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375869 | |||||||
chr8:144375911 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.12+1804T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144375911 | |||||||
chr8:144376515 | G | A | 1 | a0002c0002t0001g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.12+2408G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144376515 | |||||||
chr8:144376611 | G | A | 1 | a0002c0002t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.12+2504G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144376611 | |||||||
chr8:144376706 | C | G | 1 | a0001c0010t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12+2599C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144376706 | |||||||
chr8:144376998 | A | C | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01981.hp1 NA18951.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.13-2389A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144376998 | |||||||
chr8:144377008 | C | T | 79 | a0001c0001t0001g0140 a0001c0001t0002g0001 a0001c0001t0002g0003 others(76): Show |
143 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.13-2379C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377008 | |||||||
chr8:144377127 | A | C | 202 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(199): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.13-2260A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377127 | |||||||
chr8:144377258 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.13-2129T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377258 | |||||||
chr8:144377450 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.13-1937C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377450 | |||||||
chr8:144377451 | G | A | 1 | a0003c0004t0001g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.13-1936G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377451 | |||||||
chr8:144377626 | G | T | 1 | a0009c0013t0002g0186 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.13-1761G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377626 | |||||||
chr8:144377639 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.13-1748C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377639 | |||||||
chr8:144377663 | C | T | 9 | a0001c0003t0001g0007 a0001c0003t0001g0016 a0001c0003t0001g0017 others(6): Show |
17 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.13-1724C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377663 | |||||||
chr8:144377703 | A | G | 3 | a0002c0002t0001g0032 a0002c0002t0001g0130 a0002c0002t0001g0131 |
4 | HG02683.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-1684A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144377703 | |||||||
chr8:144378018 | G | A | 12 | a0001c0001t0001g0140 a0001c0001t0002g0006 a0001c0001t0002g0033 others(9): Show |
18 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.13-1369G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378018 | |||||||
chr8:144378027 | T | A | 1 | a0006c0008t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.13-1360T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378027 | |||||||
chr8:144378060 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.13-1327C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378060 | |||||||
chr8:144378061 | G | A | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(7): Show |
19 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-1326G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378061 | |||||||
chr8:144378120 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-1267G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378120 | |||||||
chr8:144378166 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.13-1221G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378166 | |||||||
chr8:144378305 | C | T | 10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(7): Show |
19 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.13-1082C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378305 | |||||||
chr8:144378477 | C | T | 79 | a0001c0001t0001g0140 a0001c0001t0002g0001 a0001c0001t0002g0003 others(76): Show |
143 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.13-910C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378477 | |||||||
chr8:144378615 | T | C | 113 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0001t0002g0001 others(110): Show |
199 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.13-772T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378615 | |||||||
chr8:144378868 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.13-519G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378868 | |||||||
chr8:144378936 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.13-451T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144378936 | |||||||
chr8:144379086 | A | G | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.13-301A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144379086 | |||||||
chr8:144379122 | G | A | 4 | a0001c0003t0001g0009 a0001c0003t0001g0056 a0001c0003t0001g0057 others(1): Show |
7 | HG02818.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-265G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144379122 | |||||||
chr8:144379133 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13-254A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144379133 | |||||||
chr8:144379228 | C | T | 1 | a0001c0003t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.13-159C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 1/14 | chr8 | 144379228 | |||||||
chr8:144379500 | C | G | 1 | a0001c0001t0002g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116+10C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144379500 | |||||||
chr8:144379543 | G | A | 13 | a0001c0001t0001g0140 a0001c0001t0002g0006 a0001c0001t0002g0033 others(10): Show |
19 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.116+53G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144379543 | |||||||
chr8:144379588 | C | T | 1 | a0001c0003t0001g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.116+98C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144379588 | |||||||
chr8:144379635 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116+145C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144379635 | |||||||
chr8:144379932 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.116+442C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144379932 | |||||||
chr8:144380139 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.116+649C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380139 | |||||||
chr8:144380169 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.116+679A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380169 | |||||||
chr8:144380181 | C | T | 28 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0010 others(25): Show |
50 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.116+691C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380181 | |||||||
chr8:144380186 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.116+696G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380186 | |||||||
chr8:144380344 | A | G | 6 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0001t0002g0183 others(3): Show |
6 | HG00735.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+854A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380344 | |||||||
chr8:144380480 | A | G | 8 | a0001c0003t0001g0012 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
13 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+990A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380480 | |||||||
chr8:144380534 | G | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(72): Show |
139 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.116+1044G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380534 | |||||||
chr8:144380546 | CAGGATTA others(317): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.116+1082_116+1405d others(2): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380546 | ||||||
chr8:144380559 | T | C | 5 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0048 others(2): Show |
7 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.116+1069T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380559 | |||||||
chr8:144380598 | C | CTCAGGAT others(479): Show |
1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1122_116+1123i others(488): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380598 | ||||||
chr8:144380600 | C | CAGGATTA others(641): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01175.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+1122_116+1123i others(650): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380600 | ||||||
chr8:144380600 | C | CAGGATTA others(641): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0067 others(2): Show |
6 | HG01891.hp1 HG01975.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+1122_116+1123i others(650): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380600 | ||||||
chr8:144380613 | T | C | 10 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0003t0001g0012 others(7): Show |
15 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.116+1123T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380613 | |||||||
chr8:144380642 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+1152G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380642 | |||||||
chr8:144380648 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1158T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380648 | |||||||
chr8:144380654 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1164C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380654 | |||||||
chr8:144380654 | C | CAGGATTA others(911): Show |
1 | a0001c0003t0001g0012 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.116+1176_116+1177i others(920): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(803): Show |
2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.116+1176_116+1177i others(812): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(911): Show |
8 | a0001c0003t0001g0012 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
12 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.116+1176_116+1177i others(920): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(911): Show |
3 | a0002c0002t0001g0013 a0002c0002t0001g0090 a0002c0002t0001g0110 |
6 | HG00438.hp2 HG01934.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+1176_116+1177i others(920): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(859): Show |
1 | a0002c0002t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.116+1188_116+1189i others(868): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(911): Show |
1 | a0001c0003t0001g0011 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.116+1209_116+1210i others(920): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(857): Show |
1 | a0002c0002t0001g0002 | 2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(866): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(857): Show |
66 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(63): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.116+1205_116+1206i others(866): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(1829): Show |
1 | a0002c0002t0001g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(1838): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(911): Show |
4 | a0004c0005t0001g0113 a0004c0005t0001g0116 a0004c0005t0001g0118 others(1): Show |
4 | NA18975.hp2 NA18983.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+1205_116+1206i others(920): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(857): Show |
1 | a0002c0002t0001g0002 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(866): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(803): Show |
1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(812): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
10 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(7): Show |
17 | HG00741.hp2 HG01070.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
9 | a0001c0003t0001g0007 a0001c0003t0001g0016 a0001c0003t0001g0017 others(6): Show |
17 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0003t0001g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0003t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
2 | a0001c0001t0002g0134 a0009c0013t0002g0186 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0001t0002g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0001t0002g0008 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0001t0002g0015 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
66 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(63): Show |
127 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(1019): Show |
2 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
2 | HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(1028): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(1181): Show |
2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(1190): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
3 | a0001c0001t0002g0160 a0001c0001t0002g0173 a0001c0001t0002g0178 |
3 | HG01192.hp1 HG01981.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0001t0002g0153 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380654 | C | CAGGATTA others(965): Show |
1 | a0001c0001t0002g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.116+1205_116+1206i others(974): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380654 | ||||||
chr8:144380667 | T | TGGGTGTA others(533): Show |
1 | a0001c0010t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(542): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380667 | ||||||
chr8:144380667 | T | TGGGTGTA others(641): Show |
1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(650): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380667 | ||||||
chr8:144380667 | T | TGGGTGTA others(641): Show |
1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(650): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380667 | ||||||
chr8:144380667 | T | TGGGTGTA others(533): Show |
3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.116+1205_116+1206i others(542): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380667 | ||||||
chr8:144380678 | A | ACAGATGT others(857): Show |
1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.116+1205_116+1206i others(866): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380678 | ||||||
chr8:144380678 | A | ACAGATGT others(749): Show |
1 | a0001c0001t0002g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.116+1205_116+1206i others(758): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380678 | ||||||
chr8:144380678 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1188A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380678 | |||||||
chr8:144380696 | A | G | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1206A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380696 | |||||||
chr8:144380700 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1210G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380700 | |||||||
chr8:144380702 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0001t0002g0182 others(3): Show |
6 | HG00733.hp2 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+1212C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380702 | |||||||
chr8:144380703 | G | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+1213G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380703 | |||||||
chr8:144380706 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1216C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380706 | |||||||
chr8:144380708 | A | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0194 a0001c0001t0002g0146 others(3): Show |
6 | HG00733.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.116+1218A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380708 | |||||||
chr8:144380721 | T | C | 3 | a0001c0001t0001g0070 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG03927.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1231T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380721 | |||||||
chr8:144380732 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0194 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.116+1242A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380732 | |||||||
chr8:144380754 | G | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1264G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380754 | |||||||
chr8:144380756 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(14): Show |
18 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+1266C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380756 | |||||||
chr8:144380757 | C | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(16): Show |
20 | HG00609.hp2 HG00733.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.116+1267C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380757 | |||||||
chr8:144380760 | C | G | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1270C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380760 | |||||||
chr8:144380762 | C | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0194 |
3 | HG02630.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1272C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380762 | |||||||
chr8:144380775 | T | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1285T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380775 | |||||||
chr8:144380778 | G | A | 8 | a0001c0003t0001g0012 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
13 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+1288G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380778 | |||||||
chr8:144380779 | T | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1289T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380779 | |||||||
chr8:144380786 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0194 others(2): Show |
5 | HG00733.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1296G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380786 | |||||||
chr8:144380804 | A | ACCTCCCG others(155): Show |
1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1317_116+1318i others(164): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380804 | ||||||
chr8:144380808 | G | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1318G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380808 | |||||||
chr8:144380810 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1320C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380810 | |||||||
chr8:144380811 | C | CCACTAAG others(47): Show |
1 | a0001c0001t0002g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.116+1325_116+1326i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144380811 | ||||||
chr8:144380811 | C | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0194 others(2): Show |
5 | HG00733.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.116+1321C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380811 | |||||||
chr8:144380814 | C | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1324C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380814 | |||||||
chr8:144380816 | C | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(14): Show |
18 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+1326C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380816 | |||||||
chr8:144380819 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1329G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380819 | |||||||
chr8:144380829 | T | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1339T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380829 | |||||||
chr8:144380835 | T | C | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1345T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380835 | |||||||
chr8:144380840 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1350A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380840 | |||||||
chr8:144380864 | C | T | 3 | a0001c0001t0002g0023 a0001c0001t0002g0182 a0002c0002t0001g0130 |
3 | HG03654.hp1 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1374C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380864 | |||||||
chr8:144380865 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1375G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380865 | |||||||
chr8:144380870 | A | C | 2 | a0001c0001t0002g0182 a0002c0002t0001g0077 |
2 | HG00733.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.116+1380A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380870 | |||||||
chr8:144380879 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1389G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380879 | |||||||
chr8:144380880 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1390G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380880 | |||||||
chr8:144380883 | T | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1393T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380883 | |||||||
chr8:144380894 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+1404A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380894 | |||||||
chr8:144380895 | C | G | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1405C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380895 | |||||||
chr8:144380896 | T | A | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.116+1406T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380896 | |||||||
chr8:144380912 | A | G | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1422A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380912 | |||||||
chr8:144380916 | G | C | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1426G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380916 | |||||||
chr8:144380918 | C | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1428C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380918 | |||||||
chr8:144380918 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1428C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380918 | |||||||
chr8:144380919 | C | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(14): Show |
18 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+1429C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380919 | |||||||
chr8:144380922 | C | G | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1432C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380922 | |||||||
chr8:144380924 | C | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(12): Show |
16 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.116+1434C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380924 | |||||||
chr8:144380927 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1437G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380927 | |||||||
chr8:144380937 | T | C | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1447T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380937 | |||||||
chr8:144380937 | T | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1447T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380937 | |||||||
chr8:144380948 | G | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(14): Show |
18 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.116+1458G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380948 | |||||||
chr8:144380964 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1474G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380964 | |||||||
chr8:144380966 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1476A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380966 | |||||||
chr8:144380970 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1480G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380970 | |||||||
chr8:144380973 | C | G | 3 | a0001c0001t0002g0182 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1483C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380973 | |||||||
chr8:144380978 | C | A | 3 | a0001c0001t0001g0070 a0001c0001t0002g0182 a0002c0002t0001g0077 |
3 | HG00733.hp2 HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1488C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380978 | |||||||
chr8:144380991 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1501T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380991 | |||||||
chr8:144380997 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1507T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144380997 | |||||||
chr8:144381002 | A | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(11): Show |
15 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+1512A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381002 | |||||||
chr8:144381024 | C | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(16): Show |
20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.116+1534C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381024 | |||||||
chr8:144381027 | G | C | 14 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(11): Show |
15 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.116+1537G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381027 | |||||||
chr8:144381030 | G | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(16): Show |
20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.116+1540G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381030 | |||||||
chr8:144381032 | C | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0194 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+1542C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381032 | |||||||
chr8:144381042 | T | G | 20 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(17): Show |
21 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.116+1552T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381042 | |||||||
chr8:144381045 | C | T | 18 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(15): Show |
19 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.116+1555C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381045 | |||||||
chr8:144381056 | A | ACAGATGT others(47): Show |
1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.116+1589_116+1590i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381056 | ||||||
chr8:144381057 | C | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1567C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381057 | |||||||
chr8:144381074 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1584A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381074 | |||||||
chr8:144381078 | G | C | 2 | a0001c0001t0001g0140 a0002c0002t0001g0130 |
2 | HG03927.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116+1588G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381078 | |||||||
chr8:144381080 | T | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(15): Show |
19 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.116+1590T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381080 | |||||||
chr8:144381081 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0002g0182 |
2 | HG02630.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.116+1591G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381081 | |||||||
chr8:144381084 | C | G | 2 | a0001c0001t0001g0140 a0002c0002t0001g0130 |
2 | HG03927.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116+1594C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381084 | |||||||
chr8:144381086 | A | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0001t0002g0182 others(1): Show |
4 | HG02630.hp2 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+1596A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381086 | |||||||
chr8:144381096 | G | GGCTGGGT others(155): Show |
4 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.116+1608_116+1609i others(164): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381096 | ||||||
chr8:144381096 | G | GGCTGGGT others(101): Show |
1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.116+1608_116+1609i others(110): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381096 | ||||||
chr8:144381096 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116+1606G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381096 | |||||||
chr8:144381099 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+1609C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381099 | |||||||
chr8:144381110 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116+1620A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381110 | |||||||
chr8:144381132 | G | GCCCCACT others(44): Show |
1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116+1643_116+1644i others(53): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381132 | ||||||
chr8:144381134 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.116+1644T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381134 | |||||||
chr8:144381135 | G | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+1645G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381135 | |||||||
chr8:144381135 | G | GCACTCAG others(47): Show |
1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1649_116+1650i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381135 | ||||||
chr8:144381140 | A | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.116+1650A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381140 | |||||||
chr8:144381153 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(14): Show |
21 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.116+1663C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381153 | |||||||
chr8:144381164 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1674A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381164 | |||||||
chr8:144381186 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1696G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381186 | |||||||
chr8:144381188 | T | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+1698T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381188 | |||||||
chr8:144381189 | G | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1699G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381189 | |||||||
chr8:144381192 | C | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.116+1702C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381192 | |||||||
chr8:144381194 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0002g0182 |
2 | HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1704C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381194 | |||||||
chr8:144381207 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+1717C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381207 | |||||||
chr8:144381218 | A | G | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.116+1728A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381218 | |||||||
chr8:144381240 | G | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1750G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381240 | |||||||
chr8:144381242 | C | T | 2 | a0002c0002t0001g0126 a0002c0002t0001g0130 |
2 | HG03927.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.116+1752C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381242 | |||||||
chr8:144381243 | G | C | 3 | a0001c0001t0001g0070 a0001c0001t0002g0182 a0002c0002t0001g0077 |
3 | HG00733.hp2 HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1753G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381243 | |||||||
chr8:144381246 | C | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1756C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381246 | |||||||
chr8:144381248 | C | A | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.116+1758C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381248 | |||||||
chr8:144381258 | G | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1768G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381258 | |||||||
chr8:144381261 | T | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG01106.hp1 HG01175.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.116+1771T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381261 | |||||||
chr8:144381272 | T | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.116+1782T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381272 | |||||||
chr8:144381272 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0002g0182 |
2 | HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116+1782T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381272 | |||||||
chr8:144381290 | C | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-1791C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381290 | |||||||
chr8:144381296 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0002g0182 a0002c0002t0001g0077 |
3 | HG00733.hp2 HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.117-1785T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381296 | |||||||
chr8:144381297 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0002g0182 |
2 | HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.117-1784G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381297 | |||||||
chr8:144381302 | C | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.117-1779C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381302 | |||||||
chr8:144381315 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.117-1766C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381315 | |||||||
chr8:144381315 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0182 a0002c0002t0001g0077 others(1): Show |
4 | HG00733.hp2 HG03688.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-1766C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381315 | |||||||
chr8:144381326 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1755A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381326 | |||||||
chr8:144381348 | C | G | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117-1733C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381348 | |||||||
chr8:144381350 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
7 | HG01891.hp1 HG01975.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-1731C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381350 | |||||||
chr8:144381351 | G | A | 1 | a0001c0003t0001g0010 | 4 | HG02109.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-1730G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381351 | |||||||
chr8:144381351 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1730G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381351 | |||||||
chr8:144381354 | G | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117-1727G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381354 | |||||||
chr8:144381356 | C | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0065 others(6): Show |
10 | HG00733.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-1725C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381356 | |||||||
chr8:144381359 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-1722A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381359 | |||||||
chr8:144381366 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0002g0182 |
2 | HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.117-1715G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381366 | |||||||
chr8:144381369 | C | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1712C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381369 | |||||||
chr8:144381398 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.117-1683A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381398 | |||||||
chr8:144381404 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117-1677T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381404 | |||||||
chr8:144381405 | G | C | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1676G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381405 | |||||||
chr8:144381410 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0002g0182 |
2 | HG03688.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.117-1671C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381410 | |||||||
chr8:144381423 | C | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1658C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381423 | |||||||
chr8:144381424 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-1657A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381424 | |||||||
chr8:144381434 | A | ACAGATGT others(47): Show |
2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-1629_117-1576d others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381434 | ||||||
chr8:144381434 | A | G | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1647A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381434 | |||||||
chr8:144381434 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01175.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.117-1647A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381434 | |||||||
chr8:144381452 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0180 |
3 | HG01175.hp1 HG02647.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.117-1629A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381452 | |||||||
chr8:144381458 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1623C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381458 | |||||||
chr8:144381459 | G | C | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1622G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381459 | |||||||
chr8:144381464 | C | A | 2 | a0001c0001t0002g0182 a0002c0002t0001g0130 |
2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1617C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381464 | |||||||
chr8:144381477 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(12): Show |
16 | HG01106.hp1 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.117-1604T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381477 | |||||||
chr8:144381488 | T | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0182 others(2): Show |
5 | HG00733.hp2 HG01175.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-1593T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381488 | |||||||
chr8:144381506 | C | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0182 others(2): Show |
5 | HG00733.hp2 HG01175.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-1575C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381506 | |||||||
chr8:144381510 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01175.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.117-1571G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381510 | |||||||
chr8:144381512 | T | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.117-1569T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381512 | |||||||
chr8:144381513 | G | C | 1 | a0001c0001t0002g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.117-1568G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381513 | |||||||
chr8:144381513 | G | GCACTAAG others(47): Show |
1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1564_117-1563i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381513 | ||||||
chr8:144381516 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01175.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.117-1565C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381516 | |||||||
chr8:144381518 | C | A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1563C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381518 | |||||||
chr8:144381521 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01175.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.117-1560G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381521 | |||||||
chr8:144381521 | G | GATTATGG others(47): Show |
8 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0065 others(5): Show |
9 | HG01884.hp2 HG01891.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.117-1550_117-1549i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381521 | ||||||
chr8:144381531 | C | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0130 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1550C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381531 | |||||||
chr8:144381532 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-1549A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381532 | |||||||
chr8:144381542 | A | G | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1539A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381542 | |||||||
chr8:144381560 | A | C | 3 | a0001c0003t0001g0012 a0001c0003t0001g0073 a0001c0003t0001g0074 |
6 | HG01109.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.117-1521A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381560 | |||||||
chr8:144381566 | C | CGCACTCA others(263): Show |
1 | a0001c0001t0002g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.117-1410_117-1409i others(272): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381566 | ||||||
chr8:144381566 | C | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(11): Show |
18 | HG01109.hp2 HG01175.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.117-1515C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381566 | |||||||
chr8:144381567 | G | C | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1514G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381567 | |||||||
chr8:144381585 | C | A | 1 | a0001c0003t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117-1496C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381585 | |||||||
chr8:144381585 | C | T | 2 | a0001c0001t0002g0182 a0002c0002t0001g0077 |
2 | HG00733.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.117-1496C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381585 | |||||||
chr8:144381586 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-1495G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381586 | |||||||
chr8:144381591 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(9): Show |
13 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.117-1490C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381591 | |||||||
chr8:144381596 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1485A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381596 | |||||||
chr8:144381614 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1467A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381614 | |||||||
chr8:144381614 | A | G | 28 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0010 others(25): Show |
50 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.117-1467A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381614 | |||||||
chr8:144381618 | C | G | 2 | a0001c0001t0002g0182 a0002c0002t0001g0130 |
2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1463C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381618 | |||||||
chr8:144381620 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1461C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381620 | |||||||
chr8:144381621 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0010t0001g0040 |
3 | HG02109.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117-1460G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381621 | |||||||
chr8:144381624 | G | C | 2 | a0001c0001t0002g0182 a0002c0002t0001g0130 |
2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1457G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381624 | |||||||
chr8:144381636 | G | T | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1445G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381636 | |||||||
chr8:144381668 | A | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1413A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381668 | |||||||
chr8:144381672 | C | G | 3 | a0001c0003t0001g0044 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG02965.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1409C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381672 | |||||||
chr8:144381674 | C | T | 2 | a0001c0003t0001g0044 a0002c0002t0001g0077 |
2 | HG00733.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.117-1407C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381674 | |||||||
chr8:144381678 | G | C | 3 | a0001c0003t0001g0044 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG02965.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1403G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381678 | |||||||
chr8:144381680 | C | A | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1401C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381680 | |||||||
chr8:144381683 | A | G | 3 | a0001c0003t0001g0044 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG02965.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1398A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381683 | |||||||
chr8:144381722 | A | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1359A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381722 | |||||||
chr8:144381728 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1353T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381728 | |||||||
chr8:144381734 | C | A | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1347C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381734 | |||||||
chr8:144381748 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1333G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381748 | |||||||
chr8:144381753 | C | CAGAAACA others(47): Show |
1 | a0001c0001t0002g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.117-1306_117-1305i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381753 | ||||||
chr8:144381753 | C | CAGAAACA others(263): Show |
1 | a0001c0001t0002g0176 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.117-1306_117-1305i others(272): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381753 | ||||||
chr8:144381753 | C | T | 3 | a0001c0001t0002g0182 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1328C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381753 | |||||||
chr8:144381776 | C | A | 199 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(196): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.117-1305C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381776 | |||||||
chr8:144381782 | T | C | 31 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(28): Show |
35 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.117-1299T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381782 | |||||||
chr8:144381799 | G | A | 1 | a0002c0002t0001g0019 | 3 | HG00673.hp1 HG02135.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.117-1282G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381799 | |||||||
chr8:144381801 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1280C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381801 | |||||||
chr8:144381812 | A | T | 2 | a0001c0001t0002g0182 a0002c0002t0001g0130 |
2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1269A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381812 | |||||||
chr8:144381830 | C | A | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1251C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381830 | |||||||
chr8:144381836 | T | C | 175 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(172): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.117-1245T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381836 | |||||||
chr8:144381845 | G | GATTATGG others(155): Show |
1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1226_117-1225i others(164): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381845 | ||||||
chr8:144381855 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1226C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381855 | |||||||
chr8:144381866 | A | T | 1 | a0002c0002t0001g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.117-1215A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381866 | |||||||
chr8:144381884 | C | A | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1197C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381884 | |||||||
chr8:144381890 | C | T | 3 | a0001c0001t0002g0182 a0002c0002t0001g0077 a0002c0002t0001g0130 |
3 | HG00733.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.117-1191C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381890 | |||||||
chr8:144381909 | C | T | 7 | a0001c0003t0001g0007 a0001c0003t0001g0017 a0001c0003t0001g0041 others(4): Show |
13 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.117-1172C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381909 | |||||||
chr8:144381915 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1166T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381915 | |||||||
chr8:144381938 | A | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(7): Show |
11 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.117-1143A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381938 | |||||||
chr8:144381938 | ACCTGCCG others(47): Show |
A | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-1137_117-1084d others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381938 | ||||||
chr8:144381944 | C | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117-1137C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381944 | |||||||
chr8:144381974 | T | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(8): Show |
12 | HG00733.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117-1107T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381974 | |||||||
chr8:144381974 | TCAGATGT others(47): Show |
T | 6 | a0001c0003t0001g0012 a0001c0003t0001g0025 a0001c0003t0001g0048 others(3): Show |
10 | HG01109.hp2 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-1035_117-982de others(55): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144381974 | ||||||
chr8:144381992 | C | A | 2 | a0001c0001t0001g0065 a0002c0002t0001g0077 |
2 | HG00733.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.117-1089C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381992 | |||||||
chr8:144381998 | T | C | 2 | a0001c0001t0002g0152 a0001c0001t0002g0182 |
2 | HG02056.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.117-1083T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144381998 | |||||||
chr8:144382004 | C | A | 25 | a0001c0001t0001g0065 a0001c0003t0001g0007 a0001c0003t0001g0009 others(22): Show |
43 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.117-1077C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382004 | |||||||
chr8:144382046 | C | A | 34 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(31): Show |
53 | HG00323.hp2 HG00621.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.117-1035C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382046 | |||||||
chr8:144382052 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-1029T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382052 | |||||||
chr8:144382058 | C | A | 40 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(37): Show |
63 | HG00323.hp2 HG00621.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.117-1023C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382058 | |||||||
chr8:144382058 | C | CAGGATTA others(47): Show |
1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117-1010_117-1009i others(56): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(47): Show |
3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.117-867_117-814dup others(54): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(101): Show |
77 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0002g0001 others(74): Show |
140 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.117-921_117-814dup others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(4205): Show |
1 | a0001c0001t0002g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.117-814_117-813ins others(4212): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(1073): Show |
1 | a0002c0002t0001g0199 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.117-916_117-915ins others(1080): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(101): Show |
1 | a0001c0001t0002g0033 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117-928_117-927ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(101): Show |
1 | a0001c0001t0002g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.117-957_117-956ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382058 | C | CAGGATTA others(47): Show |
3 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0003c0004t0002g0086 |
3 | HG02015.hp2 HG02165.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.117-999_117-998ins others(54): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382058 | ||||||
chr8:144382067 | G | GGGCCGGG others(100): Show |
1 | a0002c0002t0001g0088 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117-1011_117-905du others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382067 | ||||||
chr8:144382106 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-975T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382106 | |||||||
chr8:144382112 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-969A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382112 | |||||||
chr8:144382136 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-945A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382136 | |||||||
chr8:144382154 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-927A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382154 | |||||||
chr8:144382160 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117-921T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382160 | |||||||
chr8:144382166 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117-915A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382166 | |||||||
chr8:144382214 | T | C | 5 | a0001c0001t0001g0065 a0002c0002t0001g0077 a0002c0002t0001g0088 others(2): Show |
5 | HG00733.hp2 HG01255.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-867T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382214 | |||||||
chr8:144382214 | T | TGCACTAA others(101): Show |
1 | a0002c0002t0001g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.117-854_117-853ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382214 | T | TGCACTAA others(47): Show |
13 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
14 | HG00621.hp2 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.117-861_117-808dup others(54): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382214 | T | TGCACTAA others(101): Show |
3 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | HG00438.hp2 HG02074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.117-808_117-807ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382214 | T | TGCACTAA others(101): Show |
64 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(61): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.117-814_117-813ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382214 | T | TGCACTAA others(263): Show |
1 | a0002c0002t0001g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117-814_117-813ins others(270): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382214 | T | TGCACTAA others(317): Show |
1 | a0003c0004t0001g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.117-820_117-819ins others(324): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382214 | ||||||
chr8:144382225 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117-856T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382225 | |||||||
chr8:144382225 | T | TTATGGGC others(101): Show |
2 | a0001c0001t0001g0194 a0001c0010t0001g0040 |
2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.117-814_117-813ins others(108): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382225 | ||||||
chr8:144382288 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-793G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382288 | |||||||
chr8:144382331 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0065 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.117-750C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382331 | |||||||
chr8:144382506 | CTGCTGTA others(20): Show |
C | 1 | a0001c0003t0001g0010 | 4 | HG02109.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-549_117-523del others(27): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 144382506 | ||||||
chr8:144382608 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.117-473A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382608 | |||||||
chr8:144382627 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-454G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382627 | |||||||
chr8:144382739 | G | T | 2 | a0001c0001t0001g0140 a0001c0010t0001g0040 |
2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117-342G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382739 | |||||||
chr8:144382904 | A | C | 2 | a0002c0002t0001g0120 a0002c0002t0001g0121 |
2 | NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.117-177A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382904 | |||||||
chr8:144382933 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.117-148G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 2/14 | chr8 | 144382933 | |||||||
chr8:144383245 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266+15C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383245 | |||||||
chr8:144383265 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.266+35G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383265 | |||||||
chr8:144383736 | G | A | 1 | a0001c0010t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.266+506G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383736 | |||||||
chr8:144383799 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.266+569C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383799 | |||||||
chr8:144383871 | T | C | 27 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0010 others(24): Show |
47 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.266+641T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383871 | |||||||
chr8:144383886 | CT | C | 74 | a0001c0001t0001g0140 a0001c0001t0002g0185 a0001c0001t0003g0195 others(71): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.266+680delT | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144383886 | ||||||
chr8:144383886 | CTT | C | 50 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(47): Show |
78 | HG00438.hp2 HG00741.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.266+679_266+680del others(2): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144383886 | ||||||
chr8:144383886 | CTTT | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(61): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.266+678_266+680del others(3): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144383886 | ||||||
chr8:144383896 | T | G | 1 | a0001c0001t0002g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266+666T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383896 | |||||||
chr8:144383932 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.266+702A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383932 | |||||||
chr8:144383977 | C | T | 1 | a0002c0002t0001g0115 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.266+747C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144383977 | |||||||
chr8:144384065 | T | G | 1 | a0001c0003t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+835T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384065 | |||||||
chr8:144384154 | C | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(75): Show |
141 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.266+924C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384154 | |||||||
chr8:144384230 | T | C | 1 | a0001c0003t0001g0017 | 3 | HG02559.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.266+1000T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384230 | |||||||
chr8:144384572 | C | T | 3 | a0005c0006t0002g0142 a0005c0006t0002g0169 a0005c0006t0002g0174 |
3 | NA18984.hp2 NA19003.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.266+1342C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384572 | |||||||
chr8:144384613 | C | T | 1 | a0002c0002t0001g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.266+1383C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384613 | |||||||
chr8:144384618 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.266+1388C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384618 | |||||||
chr8:144384808 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.266+1578C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144384808 | |||||||
chr8:144385008 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.266+1778G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385008 | |||||||
chr8:144385037 | T | G | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.266+1807T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385037 | |||||||
chr8:144385186 | CT | C | 6 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(3): Show |
6 | HG01070.hp2 HG01169.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.266+1972delT | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144385186 | ||||||
chr8:144385207 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01175.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.266+1977C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385207 | |||||||
chr8:144385219 | C | G | 1 | a0001c0001t0002g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.266+1989C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385219 | |||||||
chr8:144385340 | C | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0175 |
5 | HG01074.hp1 HG01261.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+2110C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385340 | |||||||
chr8:144385345 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(5): Show |
9 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.266+2115G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385345 | |||||||
chr8:144385418 | A | G | 81 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0002c0002t0001g0002 others(78): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.266+2188A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385418 | |||||||
chr8:144385464 | G | A | 3 | a0002c0002t0001g0004 a0002c0002t0001g0094 a0002c0002t0001g0125 |
8 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.266+2234G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385464 | |||||||
chr8:144385690 | A | G | 113 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0001t0002g0001 others(110): Show |
199 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.266+2460A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385690 | |||||||
chr8:144385899 | G | T | 2 | a0004c0005t0001g0113 a0004c0005t0001g0116 |
2 | NA18983.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.266+2669G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385899 | |||||||
chr8:144385910 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.266+2680G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144385910 | |||||||
chr8:144385963 | C | CA | 6 | a0001c0001t0002g0157 a0001c0001t0002g0168 a0001c0001t0002g0188 others(3): Show |
6 | HG00673.hp2 HG01361.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.266+2747dupA | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144385963 | ||||||
chr8:144386066 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0001g0098 a0002c0002t0001g0099 others(1): Show |
6 | HG00544.hp2 HG02027.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.266+2836T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386066 | |||||||
chr8:144386077 | C | G | 1 | a0001c0003t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+2847C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386077 | |||||||
chr8:144386267 | C | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0112 |
7 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.266+3037C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386267 | |||||||
chr8:144386329 | T | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0094 a0002c0002t0001g0100 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.266+3099T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386329 | |||||||
chr8:144386330 | T | A | 79 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(76): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.266+3100T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386330 | |||||||
chr8:144386331 | A | T | 89 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(86): Show |
154 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.266+3101A>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386331 | |||||||
chr8:144386519 | G | T | 79 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(76): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.266+3289G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386519 | |||||||
chr8:144386593 | A | G | 2 | a0004c0005t0001g0118 a0004c0005t0001g0119 |
2 | NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.266+3363A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386593 | |||||||
chr8:144386604 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.266+3374C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386604 | |||||||
chr8:144386939 | A | G | 1 | a0002c0002t0001g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.266+3709A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144386939 | |||||||
chr8:144387043 | C | A | 3 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0095 |
3 | NA19000.hp1 NA19060.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.267-3628C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387043 | |||||||
chr8:144387078 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.267-3593A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387078 | |||||||
chr8:144387276 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.267-3395C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387276 | |||||||
chr8:144387698 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.267-2973C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387698 | |||||||
chr8:144387734 | CT | C | 35 | a0001c0001t0002g0170 a0001c0001t0002g0180 a0001c0003t0001g0007 others(32): Show |
57 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.267-2923delT | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144387734 | ||||||
chr8:144387804 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.267-2867T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387804 | |||||||
chr8:144387881 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.267-2790C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387881 | |||||||
chr8:144387921 | C | T | 2 | a0002c0002t0001g0083 a0002c0002t0001g0091 |
2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.267-2750C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144387921 | |||||||
chr8:144388174 | G | A | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.267-2497G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388174 | |||||||
chr8:144388263 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.267-2408G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388263 | |||||||
chr8:144388289 | G | A | 1 | a0002c0002t0001g0103 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.267-2382G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388289 | |||||||
chr8:144388318 | C | T | 5 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.267-2353C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388318 | |||||||
chr8:144388356 | CA | C | 7 | a0001c0001t0002g0137 a0001c0001t0002g0166 a0001c0001t0002g0190 others(4): Show |
7 | HG02976.hp1 NA18951.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.267-2299delA | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144388356 | ||||||
chr8:144388435 | C | A | 1 | a0002c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.267-2236C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388435 | |||||||
chr8:144388498 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.267-2173C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388498 | |||||||
chr8:144388553 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0003t0001g0072 |
3 | HG03139.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.267-2118G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388553 | |||||||
chr8:144388560 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.267-2111C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388560 | |||||||
chr8:144388560 | C | T | 1 | a0002c0002t0001g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.267-2111C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388560 | |||||||
chr8:144388566 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.267-2105C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388566 | |||||||
chr8:144388567 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.267-2104A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388567 | |||||||
chr8:144388575 | C | T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(72): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.267-2096C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388575 | |||||||
chr8:144388580 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267-2091C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388580 | |||||||
chr8:144388589 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.267-2082C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388589 | |||||||
chr8:144388591 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267-2080C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388591 | |||||||
chr8:144388592 | A | G | 1 | a0002c0002t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267-2079A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388592 | |||||||
chr8:144388638 | G | C | 1 | a0002c0002t0001g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.267-2033G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388638 | |||||||
chr8:144388681 | C | G | 1 | a0001c0001t0002g0165 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.267-1990C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388681 | |||||||
chr8:144388687 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0164 |
3 | HG00280.hp1 HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.267-1984C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388687 | |||||||
chr8:144388716 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267-1955G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388716 | |||||||
chr8:144388759 | T | C | 78 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(75): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.267-1912T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388759 | |||||||
chr8:144388763 | C | CA | 8 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0171 others(5): Show |
8 | HG00597.hp1 HG04184.hp1 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.267-1893dupA | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144388763 | ||||||
chr8:144388763 | CA | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0003t0001g0058 others(3): Show |
6 | HG01515.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.267-1893delA | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144388763 | ||||||
chr8:144388888 | T | G | 7 | a0001c0003t0001g0007 a0001c0003t0001g0017 a0001c0003t0001g0041 others(4): Show |
13 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.267-1783T>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144388888 | |||||||
chr8:144389176 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.267-1495A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389176 | |||||||
chr8:144389270 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0163 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.267-1401C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389270 | |||||||
chr8:144389316 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.267-1355C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389316 | |||||||
chr8:144389399 | C | A | 2 | a0002c0002t0001g0092 a0002c0002t0001g0115 |
2 | HG02074.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.267-1272C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389399 | |||||||
chr8:144389411 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.267-1260G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389411 | |||||||
chr8:144389445 | G | A | 1 | a0001c0001t0002g0023 | 3 | HG02738.hp1 HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.267-1226G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389445 | |||||||
chr8:144389450 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.267-1221T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389450 | |||||||
chr8:144389460 | T | C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0194 a0001c0003t0001g0012 others(8): Show |
16 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.267-1211T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389460 | |||||||
chr8:144389611 | G | A | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG02809.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.267-1060G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389611 | |||||||
chr8:144389652 | C | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
2 | HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.267-1019C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389652 | |||||||
chr8:144389816 | T | C | 203 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(200): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.267-855T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389816 | |||||||
chr8:144389831 | CT | C | 7 | a0001c0001t0002g0034 a0001c0001t0002g0049 a0001c0001t0002g0172 others(4): Show |
8 | HG00140.hp2 HG01255.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.267-826delT | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 144389831 | ||||||
chr8:144389921 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.267-750C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389921 | |||||||
chr8:144389941 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.267-730G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144389941 | |||||||
chr8:144390150 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.267-521G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390150 | |||||||
chr8:144390282 | G | A | 9 | a0001c0003t0001g0012 a0001c0003t0001g0025 a0001c0003t0001g0026 others(6): Show |
14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.267-389G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390282 | |||||||
chr8:144390430 | C | T | 11 | a0001c0001t0001g0140 a0001c0001t0002g0179 a0001c0003t0001g0012 others(8): Show |
16 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.267-241C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390430 | |||||||
chr8:144390520 | G | A | 1 | a0001c0003t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.267-151G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390520 | |||||||
chr8:144390576 | G | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(76): Show |
142 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.267-95G>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390576 | |||||||
chr8:144390601 | C | G | 1 | a0002c0002t0001g0101 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.267-70C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 3/14 | chr8 | 144390601 | |||||||
chr8:144391290 | C | T | 1 | a0001c0003t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.684+16C>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/14 | chr8 | 144391290 | |||||||
chr8:144391337 | T | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0163 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.685-24T>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/14 | chr8 | 144391337 | |||||||
chr8:144391342 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.685-19A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/14 | chr8 | 144391342 | |||||||
chr8:144391343 | C | A | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.685-18C>A | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/14 | chr8 | 144391343 | |||||||
chr8:144391344 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.685-17A>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 6/14 | chr8 | 144391344 | |||||||
chr8:144391514 | CGTAGGCA others(19): Show |
C | 1 | a0002c0002t0001g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-50_799-25delAG others(24): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 144391514 | ||||||
chr8:144391751 | G | C | 1 | a0001c0003t0001g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.931-32G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 8/14 | chr8 | 144391751 | |||||||
chr8:144391874 | C | CG | 22 | a0001c0001t0002g0015 a0001c0001t0002g0153 a0001c0001t0002g0157 others(19): Show |
27 | HG01192.hp1 HG01255.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1014+15dupG | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 144391874 | ||||||
chr8:144391882 | C | CG | 6 | a0001c0001t0001g0063 a0001c0001t0002g0161 a0001c0001t0002g0171 others(3): Show |
6 | HG01175.hp1 NA18955.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+21dupG | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 144391882 | ||||||
chr8:144392053 | A | G | 175 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(172): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1096+31A>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 10/14 | chr8 | 144392053 | |||||||
chr8:144392234 | G | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1176-20G>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 11/14 | chr8 | 144392234 | |||||||
chr8:144392334 | T | TGGGGGTG others(8): Show |
73 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(70): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.1260_1267+7dupGGTG others(11): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 144392334 | ||||||
chr8:144392334 | T | TGGGGGTG others(9): Show |
1 | a0006c0008t0001g0055 | 1 | HG01255.hp2 | splice_region_variant&intron_variant | LOW | c.1259_1267+7dupGGGT others(12): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 144392334 | ||||||
chr8:144392353 | C | G | 1 | a0003c0004t0001g0122 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.1267+8C>G | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | chr8 | 144392353 | |||||||
chr8:144392414 | C | CCCCT | 7 | a0001c0001t0001g0194 a0001c0001t0002g0160 a0001c0001t0002g0173 others(4): Show |
10 | HG01192.hp1 HG01981.hp2 HG02145.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1268-7_1268-4dupTC others(2): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 144392414 | ||||||
chr8:144392414 | C | CCCCTCCC others(5): Show |
2 | a0001c0001t0001g0070 a0001c0001t0002g0135 |
2 | HG02300.hp1 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.1268-15_1268-4dupT others(11): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 144392414 | ||||||
chr8:144392414 | CCCCT | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0063 others(16): Show |
25 | HG00438.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.1268-7_1268-4delTC others(2): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 144392414 | ||||||
chr8:144392426 | T | C | 28 | a0001c0003t0001g0007 a0001c0003t0001g0009 a0001c0003t0001g0010 others(25): Show |
50 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1268-19T>C | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 12/14 | chr8 | 144392426 | |||||||
chr8:144392721 | G | T | 1 | a0010c0007t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1520+24G>T | ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 13/14 | chr8 | 144392721 | |||||||
chr8:144392939 | C | CACCTGTG | 10 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0003t0001g0007 others(7): Show |
18 | HG02559.hp1 HG02622.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1638-17_1638-11dup others(7): Show |
ADCK5 | ENSG00000173137.12 | transcript | ENST00000308860.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 144392939 |