Item | Value |
---|---|
geneid | 84668 |
ensemblid | ENSG00000122591.13 |
hgncid | 24587 |
symbol | HYCC1 |
name | hyccin PI4KA lipid kinase complex subunit 1 |
refseq_nuc | NM_032581.4 |
refseq_prot | NP_115970.2 |
ensembl_nuc | ENST00000432176.7 |
ensembl_prot | ENSP00000403396.2 |
mane_status | MANE Select |
chr | chr7 |
start | 22934211 |
end | 23014130 |
strand | - |
ver | v1.2 |
region | chr7:22934211-23014130 |
region5000 | chr7:22929211-23019130 |
regionname0 | HYCC1_chr7_22934211_23014130 |
regionname5000 | HYCC1_chr7_22929211_23019130 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 521 | 376 | 77 | 69 | 173 | 13 | 42 | 143 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0002 | 0/0 | 521 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0003 | 0/0 | 521 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0004 | 0/0 | 521 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0005 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0006 | 0/0 | 521 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0007 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
a0008 | 0/0 | 521 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | MFTSE others(516): Show |
chr7 | 22929211 | 23019130 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1563 | 230 | 45 | 49 | 94 | 10 | 30 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0001c0002 | 0/0 | 1563 | 144 | 32 | 20 | 77 | 3 | 12 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0001c0006 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0001c0011 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0002c0005 | 0/0 | 1563 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0003c0003 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0004c0004 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0005c0010 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0006c0008 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0007c0007 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 | ||
a0008c0009 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | ATGTT others(1558): Show |
chr7 | 22929211 | 23019130 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 13178 | 28 | 8 | 7 | 4 | 5 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0003 | 0/0 | 13179 | 26 | 2 | 6 | 16 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13174): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0004 | 0/0 | 13164 | 24 | 0 | 3 | 21 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0006 | 0/0 | 13180 | 17 | 1 | 2 | 12 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0007 | 0/0 | 13166 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0008 | 0/0 | 13164 | 13 | 0 | 9 | 0 | 1 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0009 | 0/0 | 13181 | 13 | 1 | 0 | 11 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13176): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0011 | 0/0 | 13164 | 9 | 3 | 4 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0013 | 0/0 | 13169 | 8 | 3 | 1 | 3 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0014 | 0/0 | 13170 | 7 | 0 | 0 | 0 | 0 | 7 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0015 | 0/0 | 13175 | 6 | 0 | 4 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13170): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0016 | 0/0 | 13182 | 6 | 2 | 2 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13177): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0017 | 0/0 | 13167 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0019 | 0/0 | 13170 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0020 | 0/0 | 13177 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13172): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0024 | 0/0 | 13158 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13153): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0025 | 0/0 | 13182 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13177): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0026 | 0/0 | 13165 | 2 | 0 | 0 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0027 | 0/0 | 13180 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0028 | 0/0 | 13169 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0030 | 0/0 | 13170 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0031 | 0/0 | 13165 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0032 | 0/0 | 13179 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13174): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0033 | 0/0 | 13173 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0036 | 0/0 | 13169 | 2 | 0 | 1 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0037 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0043 | 0/0 | 13158 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13153): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0044 | 0/0 | 13157 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13152): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0045 | 0/0 | 13178 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0047 | 0/0 | 13183 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13178): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0048 | 0/0 | 13184 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13179): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0049 | 0/0 | 13183 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13178): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0050 | 0/0 | 13168 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13163): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0051 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13158): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0052 | 0/1 | 13164 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0053 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0054 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0055 | 0/0 | 13173 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0056 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13169): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0057 | 0/0 | 13174 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13169): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0058 | 0/0 | 13180 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0059 | 0/0 | 13179 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13174): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0060 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0061 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0062 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13169): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0063 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0064 | 0/0 | 13178 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0065 | 0/0 | 13162 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13157): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0066 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0067 | 0/0 | 13178 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0068 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0069 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0070 | 0/0 | 13168 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13163): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0071 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0072 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13158): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0075 | 0/0 | 13179 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13174): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0076 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0077 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13169): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0078 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0079 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0081 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13158): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0082 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0085 | 0/0 | 13167 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0086 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0093 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0001t0113 | 0/0 | 13179 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13174): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0001 | 0/0 | 13164 | 29 | 1 | 3 | 22 | 1 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0005 | 0/0 | 13164 | 24 | 0 | 2 | 17 | 1 | 4 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0007 | 0/0 | 13166 | 17 | 0 | 3 | 14 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0010 | 0/0 | 13170 | 10 | 5 | 4 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0012 | 0/0 | 13166 | 9 | 9 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0018 | 0/0 | 13152 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13147): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0021 | 0/0 | 13167 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0022 | 0/0 | 13171 | 3 | 1 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0023 | 0/0 | 13152 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13147): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0034 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0035 | 0/0 | 13175 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13170): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0038 | 0/0 | 13165 | 2 | 0 | 0 | 1 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0039 | 0/0 | 13165 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0040 | 0/0 | 13164 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0041 | 0/0 | 13165 | 2 | 0 | 1 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0042 | 0/0 | 13169 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0046 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13167): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0083 | 0/0 | 13169 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0084 | 0/0 | 13166 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0087 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0088 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0089 | 0/0 | 13166 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0090 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13167): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0091 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0092 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13169): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0094 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13167): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0095 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0096 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0097 | 0/0 | 13166 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0098 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13166): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0099 | 0/0 | 13166 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13161): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0100 | 0/0 | 13167 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0101 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0102 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0103 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13162): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0104 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0105 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13158): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0106 | 0/0 | 13165 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0107 | 0/0 | 13165 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0108 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0109 | 0/0 | 13165 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13160): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0110 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0111 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
a0001c0002t0112 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0001c0006t0006 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0001c0011t0006 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13175): Show |
chr7 | 22929211 | 23019130 |
a0002c0005t0001 | 0/0 | 13164 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0003c0003t0074 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0003c0003t0080 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13168): Show |
chr7 | 22929211 | 23019130 |
a0004c0004t0029 | 0/0 | 13178 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0005c0010t0002 | 0/0 | 13178 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13173): Show |
chr7 | 22929211 | 23019130 |
a0006c0008t0008 | 0/0 | 13164 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13159): Show |
chr7 | 22929211 | 23019130 |
a0007c0007t0013 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13164): Show |
chr7 | 22929211 | 23019130 |
a0008c0009t0073 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | AGAGA others(13165): Show |
chr7 | 22929211 | 23019130 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0004 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0011g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0011g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0011g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0024g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0024g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0025g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0025g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0026g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0026g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0027g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0028g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0028g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0031g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0031g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0032g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0032g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0033g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0033g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0036g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0036g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0037g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0037g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0043g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0044g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0045g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0047g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0048g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0049g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0050g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0051g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0052g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0053g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0054g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0055g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0056g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0057g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0058g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0059g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0060g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0061g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0062g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0063g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0064g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0065g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0066g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0067g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0068g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0069g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0070g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0071g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0072g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0075g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0076g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0077g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0078g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0079g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0081g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0082g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0085g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0086g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0093g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0113g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0008 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0023g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0023g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0034g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0034g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0035g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0035g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0038g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0038g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0039g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0039g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0040g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0041g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0041g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0042g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0042g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0046g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0083g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0084g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0087g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0088g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0089g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0090g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0091g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0092g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0094g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0095g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0096g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0097g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0098g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0099g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0100g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0101g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0102g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0103g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0104g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0105g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0106g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0107g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0108g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0109g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0110g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0111g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0112g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0006t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0011t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0002c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0003c0003t0074g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0003c0003t0080g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0004c0004t0029g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0005c0010t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0006c0008t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0007c0007t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0008c0009t0073g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0036 | g0110 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00280 | hp1 | a0001 | c0001 | t0045 | g0032 | EUR | FIN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00280 | hp2 | a0001 | c0002 | t0005 | g0252 | EUR | FIN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0156 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0062 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00544 | hp1 | a0001 | c0001 | t0013 | g0172 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00544 | hp2 | a0001 | c0001 | t0050 | g0306 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00558 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00639 | hp1 | a0001 | c0001 | t0059 | g0100 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0068 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0023 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00733 | hp1 | a0001 | c0002 | t0010 | g0020 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00733 | hp2 | a0001 | c0001 | t0058 | g0094 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00738 | hp1 | a0001 | c0001 | t0011 | g0003 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0040 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0320 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01069 | hp2 | a0001 | c0001 | t0019 | g0117 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0331 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01071 | hp1 | a0001 | c0001 | t0061 | g0118 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01074 | hp1 | a0001 | c0002 | t0010 | g0020 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01074 | hp2 | a0001 | c0002 | t0040 | g0019 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01081 | hp1 | a0001 | c0001 | t0013 | g0302 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01081 | hp2 | a0001 | c0001 | t0033 | g0050 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01099 | hp2 | a0001 | c0002 | t0010 | g0260 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01106 | hp1 | a0001 | c0001 | t0011 | g0011 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01109 | hp1 | a0001 | c0002 | t0022 | g0261 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0318 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01169 | hp1 | a0001 | c0002 | t0007 | g0204 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01169 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01175 | hp2 | a0001 | c0002 | t0106 | g0222 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01192 | hp1 | a0001 | c0002 | t0083 | g0288 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0023 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01243 | hp2 | a0001 | c0002 | t0098 | g0297 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01255 | hp1 | a0005 | c0010 | t0002 | g0187 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0335 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0027 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0312 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01257 | hp1 | a0001 | c0001 | t0027 | g0014 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01257 | hp2 | a0001 | c0002 | t0010 | g0227 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01258 | hp1 | a0001 | c0001 | t0027 | g0014 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01258 | hp2 | a0001 | c0002 | t0005 | g0027 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0308 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01358 | hp1 | a0001 | c0001 | t0011 | g0003 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01361 | hp2 | a0001 | c0001 | t0024 | g0030 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01433 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0330 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01515 | hp1 | a0001 | c0001 | t0015 | g0002 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01516 | hp1 | a0006 | c0008 | t0008 | g0047 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01884 | hp1 | a0001 | c0002 | t0012 | g0192 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0045 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01928 | hp2 | a0001 | c0002 | t0041 | g0282 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0327 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01978 | hp2 | a0001 | c0001 | t0070 | g0042 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01993 | hp1 | a0001 | c0001 | t0036 | g0071 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01993 | hp2 | a0001 | c0001 | t0020 | g0091 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0215 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02040 | hp1 | a0001 | c0006 | t0006 | g0171 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02040 | hp2 | a0001 | c0002 | t0102 | g0241 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02055 | hp1 | a0001 | c0002 | t0035 | g0059 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02055 | hp2 | a0001 | c0001 | t0076 | g0054 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0250 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02071 | hp1 | a0001 | c0001 | t0093 | g0116 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02071 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02074 | hp2 | a0001 | c0002 | t0005 | g0245 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02083 | hp1 | a0001 | c0002 | t0005 | g0247 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02132 | hp1 | a0001 | c0002 | t0042 | g0278 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02132 | hp2 | a0007 | c0007 | t0013 | g0060 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02135 | hp1 | a0001 | c0001 | t0013 | g0142 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02135 | hp2 | a0001 | c0002 | t0039 | g0246 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02145 | hp1 | a0001 | c0001 | t0030 | g0127 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02145 | hp2 | a0003 | c0003 | t0074 | g0053 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02155 | hp1 | a0001 | c0002 | t0038 | g0235 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02155 | hp2 | a0001 | c0002 | t0007 | g0015 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02165 | hp2 | a0001 | c0002 | t0005 | g0249 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02257 | hp1 | a0001 | c0002 | t0010 | g0290 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0011 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02273 | hp1 | a0001 | c0002 | t0100 | g0206 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0315 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0309 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02293 | hp2 | a0001 | c0002 | t0089 | g0201 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02300 | hp1 | a0001 | c0002 | t0007 | g0210 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0319 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02572 | hp1 | a0001 | c0002 | t0012 | g0193 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02572 | hp2 | a0001 | c0002 | t0090 | g0287 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02602 | hp1 | a0001 | c0002 | t0040 | g0019 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02622 | hp1 | a0001 | c0001 | t0033 | g0049 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02622 | hp2 | a0001 | c0001 | t0075 | g0338 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02630 | hp1 | a0001 | c0001 | t0078 | g0056 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02630 | hp2 | a0001 | c0002 | t0094 | g0224 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02698 | hp2 | a0001 | c0001 | t0085 | g0112 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02717 | hp1 | a0001 | c0002 | t0012 | g0196 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02735 | hp1 | a0001 | c0001 | t0057 | g0041 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0003 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0154 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0314 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02809 | hp1 | a0001 | c0002 | t0088 | g0294 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02818 | hp1 | a0004 | c0004 | t0029 | g0012 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02818 | hp2 | a0001 | c0002 | t0010 | g0264 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02886 | hp1 | a0001 | c0002 | t0034 | g0299 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02886 | hp2 | a0001 | c0002 | t0021 | g0194 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02896 | hp1 | a0001 | c0002 | t0012 | g0257 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02896 | hp2 | a0001 | c0001 | t0037 | g0034 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0075 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02897 | hp2 | a0001 | c0002 | t0012 | g0256 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0147 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02965 | hp1 | a0001 | c0001 | t0031 | g0102 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02970 | hp1 | a0001 | c0002 | t0046 | g0038 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02970 | hp2 | a0001 | c0002 | t0012 | g0200 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02976 | hp1 | a0001 | c0001 | t0044 | g0031 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02976 | hp2 | a0008 | c0009 | t0073 | g0337 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03017 | hp1 | a0001 | c0001 | t0015 | g0039 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03017 | hp2 | a0001 | c0001 | t0067 | g0178 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03041 | hp2 | a0001 | c0002 | t0010 | g0295 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03098 | hp1 | a0003 | c0003 | t0080 | g0052 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03098 | hp2 | a0001 | c0002 | t0021 | g0230 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03130 | hp2 | a0001 | c0001 | t0069 | g0126 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03139 | hp1 | a0001 | c0001 | t0019 | g0334 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03139 | hp2 | a0001 | c0002 | t0084 | g0199 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03195 | hp1 | a0001 | c0001 | t0062 | g0066 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03195 | hp2 | a0001 | c0001 | t0030 | g0077 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03209 | hp1 | a0001 | c0002 | t0091 | g0058 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03209 | hp2 | a0001 | c0002 | t0012 | g0189 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03239 | hp1 | a0001 | c0001 | t0082 | g0131 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03239 | hp2 | a0001 | c0002 | t0005 | g0236 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03453 | hp2 | a0001 | c0002 | t0021 | g0289 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03486 | hp1 | a0001 | c0001 | t0081 | g0188 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03486 | hp2 | a0001 | c0002 | t0097 | g0195 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03490 | hp1 | a0001 | c0001 | t0014 | g0084 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03491 | hp2 | a0001 | c0001 | t0026 | g0311 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03492 | hp1 | a0001 | c0001 | t0026 | g0321 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03492 | hp2 | a0001 | c0001 | t0014 | g0111 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03540 | hp1 | a0004 | c0004 | t0029 | g0012 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03540 | hp2 | a0001 | c0001 | t0077 | g0051 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03579 | hp1 | a0001 | c0002 | t0010 | g0292 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03579 | hp2 | a0001 | c0001 | t0043 | g0028 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03688 | hp1 | a0001 | c0001 | t0086 | g0124 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0316 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03704 | hp1 | a0001 | c0001 | t0065 | g0083 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03704 | hp2 | a0001 | c0002 | t0095 | g0229 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0122 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03831 | hp1 | a0001 | c0002 | t0038 | g0259 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03831 | hp2 | a0001 | c0002 | t0022 | g0296 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03834 | hp1 | a0001 | c0001 | t0014 | g0109 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0253 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03927 | hp1 | a0001 | c0002 | t0005 | g0238 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03927 | hp2 | a0001 | c0001 | t0055 | g0043 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03942 | hp1 | a0001 | c0001 | t0014 | g0108 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0155 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04115 | hp1 | a0001 | c0001 | t0014 | g0113 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0239 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04184 | hp1 | a0001 | c0001 | t0011 | g0003 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04199 | hp1 | a0001 | c0001 | t0014 | g0114 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0022 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04204 | hp1 | a0001 | c0001 | t0014 | g0115 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04228 | hp1 | a0001 | c0002 | t0010 | g0262 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04228 | hp2 | a0001 | c0002 | t0099 | g0216 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18522 | hp1 | a0001 | c0001 | t0037 | g0035 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18612 | hp1 | a0001 | c0001 | t0013 | g0061 | EAS | CHB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18612 | hp2 | a0001 | c0001 | t0053 | g0323 | EAS | CHB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18906 | hp1 | a0001 | c0002 | t0010 | g0293 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18906 | hp2 | a0001 | c0002 | t0012 | g0190 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18939 | hp2 | a0001 | c0001 | t0025 | g0186 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18942 | hp1 | a0001 | c0001 | t0028 | g0152 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18942 | hp2 | a0001 | c0001 | t0028 | g0129 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18943 | hp2 | a0001 | c0002 | t0018 | g0017 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18952 | hp1 | a0001 | c0001 | t0032 | g0303 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18954 | hp1 | a0001 | c0002 | t0109 | g0268 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18956 | hp1 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18960 | hp1 | a0001 | c0002 | t0007 | g0015 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18961 | hp2 | a0001 | c0002 | t0005 | g0237 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18965 | hp1 | a0001 | c0002 | t0005 | g0255 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18965 | hp2 | a0001 | c0001 | t0017 | g0132 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18966 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18968 | hp1 | a0001 | c0002 | t0005 | g0234 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18968 | hp2 | a0001 | c0001 | t0009 | g0150 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18970 | hp2 | a0001 | c0002 | t0007 | g0305 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18973 | hp1 | a0001 | c0001 | t0063 | g0151 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18975 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18977 | hp1 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18978 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18978 | hp2 | a0001 | c0002 | t0039 | g0244 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18983 | hp1 | a0001 | c0002 | t0087 | g0209 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18984 | hp1 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18984 | hp2 | a0001 | c0002 | t0023 | g0016 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18986 | hp2 | a0001 | c0001 | t0051 | g0322 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18987 | hp2 | a0001 | c0002 | t0103 | g0254 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18988 | hp1 | a0001 | c0001 | t0032 | g0304 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18988 | hp2 | a0001 | c0002 | t0007 | g0212 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18989 | hp1 | a0001 | c0002 | t0007 | g0214 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18991 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18991 | hp2 | a0001 | c0002 | t0108 | g0283 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18992 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18992 | hp2 | a0001 | c0002 | t0101 | g0213 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18994 | hp2 | a0001 | c0002 | t0007 | g0218 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18998 | hp1 | a0001 | c0002 | t0041 | g0225 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18998 | hp2 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0098 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19000 | hp1 | a0001 | c0002 | t0007 | g0208 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19001 | hp1 | a0001 | c0001 | t0072 | g0329 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19003 | hp2 | a0001 | c0011 | t0006 | g0165 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19004 | hp2 | a0001 | c0002 | t0007 | g0207 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19005 | hp1 | a0001 | c0002 | t0018 | g0211 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19005 | hp2 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19010 | hp1 | a0001 | c0001 | t0047 | g0185 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19010 | hp2 | a0001 | c0001 | t0054 | g0307 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19012 | hp1 | a0001 | c0002 | t0005 | g0243 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19012 | hp2 | a0001 | c0002 | t0007 | g0217 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19043 | hp1 | a0001 | c0002 | t0096 | g0197 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19054 | hp1 | a0001 | c0002 | t0005 | g0240 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0092 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19056 | hp2 | a0001 | c0001 | t0025 | g0137 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19058 | hp2 | a0001 | c0002 | t0023 | g0220 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19059 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19062 | hp1 | a0001 | c0002 | t0023 | g0016 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19062 | hp2 | a0001 | c0001 | t0049 | g0138 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19065 | hp1 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19066 | hp1 | a0001 | c0002 | t0005 | g0242 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19066 | hp2 | a0001 | c0002 | t0018 | g0221 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19067 | hp1 | a0001 | c0002 | t0005 | g0231 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19068 | hp1 | a0001 | c0002 | t0018 | g0017 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19068 | hp2 | a0001 | c0001 | t0017 | g0085 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19074 | hp1 | a0001 | c0001 | t0113 | g0341 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19076 | hp1 | a0001 | c0002 | t0007 | g0205 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19076 | hp2 | a0001 | c0002 | t0005 | g0251 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19077 | hp1 | a0001 | c0002 | t0105 | g0036 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19077 | hp2 | a0001 | c0001 | t0060 | g0141 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19079 | hp1 | a0001 | c0002 | t0104 | g0037 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19079 | hp2 | a0001 | c0001 | t0064 | g0153 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19081 | hp1 | a0001 | c0002 | t0042 | g0272 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19082 | hp1 | a0001 | c0001 | t0048 | g0184 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19083 | hp1 | a0001 | c0001 | t0016 | g0180 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19083 | hp2 | a0001 | c0002 | t0110 | g0276 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19084 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19084 | hp2 | a0001 | c0002 | t0005 | g0248 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19086 | hp1 | a0001 | c0001 | t0009 | g0145 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19086 | hp2 | a0001 | c0002 | t0107 | g0269 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19087 | hp1 | a0001 | c0001 | t0016 | g0146 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19088 | hp2 | a0001 | c0001 | t0009 | g0159 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19089 | hp1 | a0001 | c0001 | t0071 | g0093 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19090 | hp2 | a0001 | c0002 | t0112 | g0340 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19240 | hp1 | a0001 | c0001 | t0020 | g0097 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19240 | hp2 | a0001 | c0002 | t0012 | g0191 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ASW | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20129 | hp2 | a0001 | c0002 | t0022 | g0291 | AFR | ASW | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20752 | hp2 | a0001 | c0002 | t0111 | g0300 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0022 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0167 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02109 | hp1 | a0001 | c0001 | t0056 | g0044 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02109 | hp2 | a0001 | c0001 | t0031 | g0099 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02486 | hp1 | a0001 | c0001 | t0079 | g0055 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02486 | hp2 | a0001 | c0002 | t0092 | g0198 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02559 | hp1 | a0001 | c0001 | t0068 | g0125 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0029 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03471 | hp1 | a0001 | c0001 | t0019 | g0333 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03471 | hp2 | a0001 | c0002 | t0034 | g0226 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG06807 | hp1 | a0001 | c0002 | t0035 | g0301 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20300 | hp1 | a0001 | c0001 | t0066 | g0128 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0121 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0134 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
homoSapiens | chm13v2 | a0001 | c0001 | t0052 | g0339 | REF | REF | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0119 | REF | REF | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22945600 | A | G | 1 | a0003 | 2 | HG02145.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1555T>C | p.Ser519Pro | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1789/13178 | 1555/1566 | 519/521 | chr7 | 22945600 | |||
chr7:22945636 | C | G | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1519G>C | p.Gly507Arg | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1753/13178 | 1519/1566 | 507/521 | chr7 | 22945636 | |||
chr7:22945663 | T | C | 1 | a0004 | 2 | HG02818.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.1492A>G | p.Thr498Ala | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1726/13178 | 1492/1566 | 498/521 | chr7 | 22945663 | |||
chr7:22945740 | C | T | 1 | a0008 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1415G>A | p.Cys472Tyr | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1649/13178 | 1415/1566 | 472/521 | chr7 | 22945740 | |||
chr7:22945812 | G | T | 1 | a0006 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1343C>A | p.Thr448Asn | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1577/13178 | 1343/1566 | 448/521 | chr7 | 22945812 | |||
chr7:22945816 | C | T | 1 | a0002 | 2 | HG00558.hp1 NA18992.hp1 |
missense_variant | MODERATE | c.1339G>A | p.Ala447Thr | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1573/13178 | 1339/1566 | 447/521 | chr7 | 22945816 | |||
chr7:22945984 | C | G | 1 | a0007 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1171G>C | p.Gly391Arg | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1405/13178 | 1171/1566 | 391/521 | chr7 | 22945984 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22960413 | A | C | 1 | a0001c0006 | 1 | HG02040.hp1 | splice_region_variant&synonymous_variant | LOW | c.834T>G | p.Val278Val | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/11 | 1068/13178 | 834/1566 | 278/521 | chr7 | 22960413 | |||
chr7:22976212 | T | C | 2 | a0001c0002 a0002c0005 |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
splice_region_variant&synonymous_variant | LOW | c.624A>G | p.Ser208Ser | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/11 | 858/13178 | 624/1566 | 208/521 | chr7 | 22976212 | |||
chr7:22976221 | T | C | 1 | a0001c0011 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.615A>G | p.Gln205Gln | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/11 | 849/13178 | 615/1566 | 205/521 | chr7 | 22976221 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22934233 | T | C | 1 | a0001c0001t0081 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11356A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11356 | chr7 | 22934233 | ||||||
chr7:22934234 | T | C | 19 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(16): Show |
65 | HG00423.hp1 HG00642.hp2 HG00738.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*11355A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11355 | chr7 | 22934234 | ||||||
chr7:22934234 | T | TC | 11 | a0001c0001t0048 a0001c0001t0049 a0001c0001t0056 others(8): Show |
21 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*11354dupG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11354 | chr7 | 22934234 | ||||||
chr7:22934234 | T | TTC | 6 | a0001c0001t0015 a0001c0001t0057 a0001c0002t0022 others(3): Show |
14 | HG00738.hp2 HG01109.hp1 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11354_*11355insGA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11354 | chr7 | 22934234 | ||||||
chr7:22934258 | T | TCAG | 6 | a0001c0002t0035 a0001c0002t0090 a0001c0002t0091 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11328_*11330dupCT others(1): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11330 | chr7 | 22934258 | ||||||
chr7:22934697 | C | A | 1 | a0008c0009t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10892G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10892 | chr7 | 22934697 | ||||||
chr7:22934948 | G | A | 1 | a0001c0001t0032 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10641C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10641 | chr7 | 22934948 | ||||||
chr7:22934976 | G | C | 1 | a0001c0002t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10613C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10613 | chr7 | 22934976 | ||||||
chr7:22935224 | T | G | 1 | a0001c0001t0072 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10365A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10365 | chr7 | 22935224 | ||||||
chr7:22935293 | T | G | 79 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(76): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*10296A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10296 | chr7 | 22935293 | ||||||
chr7:22935385 | C | T | 44 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(41): Show |
122 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*10204G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10204 | chr7 | 22935385 | ||||||
chr7:22935426 | C | T | 80 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(77): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*10163G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10163 | chr7 | 22935426 | ||||||
chr7:22935650 | T | C | 1 | a0001c0001t0093 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9939A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9939 | chr7 | 22935650 | ||||||
chr7:22935688 | C | T | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9901G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9901 | chr7 | 22935688 | ||||||
chr7:22935710 | A | G | 33 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0050 others(30): Show |
121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*9879T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9879 | chr7 | 22935710 | ||||||
chr7:22935864 | G | A | 1 | a0001c0002t0094 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9725C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9725 | chr7 | 22935864 | ||||||
chr7:22935873 | TTC | T | 10 | a0001c0001t0050 a0001c0001t0054 a0001c0002t0001 others(7): Show |
40 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*9714_*9715delGA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9714 | chr7 | 22935873 | ||||||
chr7:22936030 | G | T | 1 | a0001c0001t0075 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9559C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9559 | chr7 | 22936030 | ||||||
chr7:22936040 | G | A | 56 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(53): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*9549C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9549 | chr7 | 22936040 | ||||||
chr7:22936289 | G | A | 20 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(17): Show |
70 | HG00423.hp1 HG00642.hp2 HG00738.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*9300C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9300 | chr7 | 22936289 | ||||||
chr7:22936322 | C | T | 4 | a0001c0001t0014 a0001c0001t0036 a0001c0001t0082 others(1): Show |
11 | HG00099.hp1 HG01993.hp1 HG02698.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9267G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9267 | chr7 | 22936322 | ||||||
chr7:22937006 | G | C | 1 | a0001c0001t0072 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8583C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8583 | chr7 | 22937006 | ||||||
chr7:22937079 | G | A | 5 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 others(2): Show |
6 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8510C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8510 | chr7 | 22937079 | ||||||
chr7:22937175 | T | C | 7 | a0001c0001t0033 a0001c0001t0076 a0001c0001t0077 others(4): Show |
8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8414A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8414 | chr7 | 22937175 | ||||||
chr7:22937193 | G | A | 1 | a0001c0001t0045 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8396C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8396 | chr7 | 22937193 | ||||||
chr7:22937226 | A | T | 1 | a0001c0002t0088 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8363T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8363 | chr7 | 22937226 | ||||||
chr7:22937250 | C | A | 60 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(57): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*8339G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8339 | chr7 | 22937250 | ||||||
chr7:22937268 | C | CA | 17 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(14): Show |
67 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*8320dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8320 | chr7 | 22937268 | ||||||
chr7:22937489 | A | C | 1 | a0001c0002t0106 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8100T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8100 | chr7 | 22937489 | ||||||
chr7:22937493 | A | G | 1 | a0001c0001t0068 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8096T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8096 | chr7 | 22937493 | ||||||
chr7:22937535 | G | C | 2 | a0001c0001t0072 a0008c0009t0073 |
2 | HG02976.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8054C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8054 | chr7 | 22937535 | ||||||
chr7:22937537 | G | A | 1 | a0001c0002t0095 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8052C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8052 | chr7 | 22937537 | ||||||
chr7:22937633 | G | C | 1 | a0001c0001t0063 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7956C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7956 | chr7 | 22937633 | ||||||
chr7:22937902 | T | C | 1 | a0001c0001t0072 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7687A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7687 | chr7 | 22937902 | ||||||
chr7:22937904 | C | T | 1 | a0001c0001t0044 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7685G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7685 | chr7 | 22937904 | ||||||
chr7:22938049 | T | G | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7540A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7540 | chr7 | 22938049 | ||||||
chr7:22938069 | T | C | 1 | a0001c0002t0040 | 2 | HG01074.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7520A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7520 | chr7 | 22938069 | ||||||
chr7:22938160 | A | T | 1 | a0001c0001t0085 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7429T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7429 | chr7 | 22938160 | ||||||
chr7:22938193 | G | A | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7396C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7396 | chr7 | 22938193 | ||||||
chr7:22938294 | C | T | 1 | a0001c0001t0064 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7295G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7295 | chr7 | 22938294 | ||||||
chr7:22938350 | A | G | 4 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 others(1): Show |
5 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7239T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7239 | chr7 | 22938350 | ||||||
chr7:22938527 | A | C | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7062T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7062 | chr7 | 22938527 | ||||||
chr7:22938567 | T | C | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7022A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7022 | chr7 | 22938567 | ||||||
chr7:22938675 | C | G | 1 | a0001c0002t0110 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6914G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6914 | chr7 | 22938675 | ||||||
chr7:22938756 | A | T | 26 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(23): Show |
77 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*6833T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6833 | chr7 | 22938756 | ||||||
chr7:22938796 | A | G | 1 | a0001c0001t0076 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6793T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6793 | chr7 | 22938796 | ||||||
chr7:22938836 | TCA | T | 54 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(51): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*6751_*6752delTG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6751 | chr7 | 22938836 | ||||||
chr7:22938888 | T | A | 1 | a0001c0002t0096 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6701A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6701 | chr7 | 22938888 | ||||||
chr7:22938920 | T | C | 2 | a0001c0002t0104 a0001c0002t0105 |
2 | NA19077.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6669A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6669 | chr7 | 22938920 | ||||||
chr7:22938968 | G | A | 61 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(58): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*6621C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6621 | chr7 | 22938968 | ||||||
chr7:22939307 | A | G | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*6282T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6282 | chr7 | 22939307 | ||||||
chr7:22939478 | A | G | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*6111T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6111 | chr7 | 22939478 | ||||||
chr7:22939503 | T | C | 1 | a0001c0002t0097 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6086A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6086 | chr7 | 22939503 | ||||||
chr7:22939519 | C | T | 1 | a0001c0001t0027 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6070G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6070 | chr7 | 22939519 | ||||||
chr7:22939536 | C | T | 1 | a0001c0001t0078 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6053G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6053 | chr7 | 22939536 | ||||||
chr7:22939622 | C | T | 1 | a0001c0002t0099 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5967G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5967 | chr7 | 22939622 | ||||||
chr7:22939779 | C | A | 22 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(19): Show |
72 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5810G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5810 | chr7 | 22939779 | ||||||
chr7:22939914 | G | A | 2 | a0001c0001t0058 a0001c0001t0059 |
2 | HG00639.hp1 HG00733.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5675C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5675 | chr7 | 22939914 | ||||||
chr7:22939924 | T | A | 1 | a0001c0002t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5665A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5665 | chr7 | 22939924 | ||||||
chr7:22940013 | T | C | 8 | a0001c0001t0007 a0001c0002t0007 a0001c0002t0018 others(5): Show |
29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5576A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5576 | chr7 | 22940013 | ||||||
chr7:22940090 | C | A | 1 | a0001c0002t0098 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5499G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5499 | chr7 | 22940090 | ||||||
chr7:22940094 | T | G | 1 | a0001c0001t0072 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5495A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5495 | chr7 | 22940094 | ||||||
chr7:22940167 | A | C | 1 | a0001c0001t0075 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5422T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5422 | chr7 | 22940167 | ||||||
chr7:22940220 | T | C | 8 | a0001c0001t0007 a0001c0002t0007 a0001c0002t0018 others(5): Show |
29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5369A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5369 | chr7 | 22940220 | ||||||
chr7:22940236 | G | GT | 6 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0059 others(3): Show |
32 | HG00558.hp2 HG00639.hp1 HG01070.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5352dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | ||||||
chr7:22940236 | G | GTT | 8 | a0001c0001t0006 a0001c0001t0027 a0001c0001t0058 others(5): Show |
25 | HG00733.hp2 HG01099.hp1 HG01257.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5351_*5352dupAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | ||||||
chr7:22940236 | G | GTTT | 4 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0049 others(1): Show |
17 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5350_*5352dupAAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | ||||||
chr7:22940236 | G | GTTTT | 3 | a0001c0001t0016 a0001c0001t0047 a0001c0001t0048 |
8 | HG00639.hp2 HG01255.hp2 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5349_*5352dupAAAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | ||||||
chr7:22940236 | GT | G | 2 | a0001c0001t0019 a0001c0001t0020 |
6 | HG01069.hp2 HG01993.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5352delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTT | G | 6 | a0001c0001t0026 a0001c0001t0033 a0001c0001t0077 others(3): Show |
8 | HG01081.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5348_*5352delAAAA others(1): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5348 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTT | G | 12 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(9): Show |
60 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5347_*5352delAAAA others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5347 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(1): Show |
G | 13 | a0001c0001t0014 a0001c0001t0072 a0001c0001t0082 others(10): Show |
24 | HG02055.hp1 HG02155.hp1 HG02698.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5345_*5352delAAAA others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5345 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(2): Show |
G | 45 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0024 others(42): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*5344_*5352delAAAA others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5344 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(3): Show |
G | 1 | a0001c0002t0105 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5343_*5352delAAAA others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5343 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0017 | 4 | NA18965.hp2 NA18984.hp1 NA18999.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5342_*5352delAAAA others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5342 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0031 | 2 | HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5340_*5352delAAAA others(9): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5340 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0065 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5337_*5352delAAAA others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5337 | chr7 | 22940236 | ||||||
chr7:22940236 | GTTTTTTT others(16): Show |
G | 2 | a0001c0002t0018 a0001c0002t0023 |
7 | NA18943.hp2 NA18984.hp2 NA19005.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5330_*5352delAAAA others(19): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5330 | chr7 | 22940236 | ||||||
chr7:22940238 | T | G | 1 | a0001c0001t0030 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5351A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5351 | chr7 | 22940238 | ||||||
chr7:22940250 | T | G | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5339A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5339 | chr7 | 22940250 | ||||||
chr7:22940252 | T | G | 1 | a0001c0001t0026 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5337A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5337 | chr7 | 22940252 | ||||||
chr7:22940253 | T | G | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(8): Show |
59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5336A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5336 | chr7 | 22940253 | ||||||
chr7:22940256 | T | G | 1 | a0004c0004t0029 | 2 | HG02818.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5333A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5333 | chr7 | 22940256 | ||||||
chr7:22940338 | G | A | 1 | a0001c0001t0081 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5251C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5251 | chr7 | 22940338 | ||||||
chr7:22940400 | C | T | 1 | a0001c0001t0043 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5189G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5189 | chr7 | 22940400 | ||||||
chr7:22940542 | G | A | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*5047C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5047 | chr7 | 22940542 | ||||||
chr7:22940552 | A | G | 2 | a0001c0001t0019 a0001c0001t0061 |
4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5037T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5037 | chr7 | 22940552 | ||||||
chr7:22940641 | G | A | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*4948C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4948 | chr7 | 22940641 | ||||||
chr7:22940659 | C | T | 4 | a0001c0001t0015 a0001c0001t0055 a0001c0001t0056 others(1): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4930G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4930 | chr7 | 22940659 | ||||||
chr7:22940679 | C | A | 8 | a0001c0001t0033 a0001c0001t0075 a0001c0001t0076 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4910G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4910 | chr7 | 22940679 | ||||||
chr7:22940743 | G | A | 1 | a0001c0002t0023 | 3 | NA18984.hp2 NA19058.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4846C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4846 | chr7 | 22940743 | ||||||
chr7:22940750 | G | T | 1 | a0001c0002t0084 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4839C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4839 | chr7 | 22940750 | ||||||
chr7:22940797 | T | C | 1 | a0001c0001t0072 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4792A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4792 | chr7 | 22940797 | ||||||
chr7:22940819 | CT | C | 7 | a0001c0001t0030 a0001c0001t0051 a0001c0001t0057 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4769delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4769 | chr7 | 22940819 | ||||||
chr7:22940875 | A | G | 1 | a0001c0002t0083 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4714T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4714 | chr7 | 22940875 | ||||||
chr7:22941019 | C | A | 22 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(19): Show |
72 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4570 | chr7 | 22941019 | ||||||
chr7:22941221 | T | C | 1 | a0001c0001t0031 | 2 | HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4368A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4368 | chr7 | 22941221 | ||||||
chr7:22941234 | A | G | 1 | a0001c0001t0060 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4355T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4355 | chr7 | 22941234 | ||||||
chr7:22941310 | A | AAC | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*4278_*4279insGT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4278 | chr7 | 22941310 | ||||||
chr7:22941368 | C | G | 2 | a0001c0002t0107 a0001c0002t0108 |
2 | NA18991.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4221G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4221 | chr7 | 22941368 | ||||||
chr7:22941672 | T | C | 1 | a0008c0009t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3917A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3917 | chr7 | 22941672 | ||||||
chr7:22941702 | A | C | 1 | a0001c0001t0078 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3887T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3887 | chr7 | 22941702 | ||||||
chr7:22941785 | T | G | 27 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(24): Show |
78 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3804A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3804 | chr7 | 22941785 | ||||||
chr7:22941909 | T | C | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*3680A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3680 | chr7 | 22941909 | ||||||
chr7:22942081 | T | C | 1 | a0001c0001t0071 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3508A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3508 | chr7 | 22942081 | ||||||
chr7:22942323 | G | A | 1 | a0001c0001t0011 | 9 | HG00738.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3266C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3266 | chr7 | 22942323 | ||||||
chr7:22942323 | G | T | 1 | a0001c0002t0102 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3266 | chr7 | 22942323 | ||||||
chr7:22942588 | T | C | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*3001A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3001 | chr7 | 22942588 | ||||||
chr7:22942613 | C | A | 4 | a0001c0001t0015 a0001c0001t0055 a0001c0001t0056 others(1): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2976G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2976 | chr7 | 22942613 | ||||||
chr7:22942711 | A | C | 1 | a0001c0001t0032 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2878T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2878 | chr7 | 22942711 | ||||||
chr7:22942893 | T | C | 1 | a0008c0009t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2696A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2696 | chr7 | 22942893 | ||||||
chr7:22942905 | T | C | 1 | a0001c0001t0053 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2684A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2684 | chr7 | 22942905 | ||||||
chr7:22942928 | G | A | 22 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(19): Show |
72 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2661C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2661 | chr7 | 22942928 | ||||||
chr7:22943130 | G | T | 4 | a0001c0001t0015 a0001c0001t0055 a0001c0001t0056 others(1): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2459C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2459 | chr7 | 22943130 | ||||||
chr7:22943206 | CAT | C | 9 | a0001c0002t0005 a0001c0002t0038 a0001c0002t0039 others(6): Show |
35 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2381_*2382delAT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2381 | chr7 | 22943206 | ||||||
chr7:22943391 | T | C | 1 | a0001c0002t0106 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2198 | chr7 | 22943391 | ||||||
chr7:22943481 | C | T | 1 | a0001c0001t0032 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2108G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2108 | chr7 | 22943481 | ||||||
chr7:22943620 | C | T | 8 | a0001c0001t0015 a0001c0001t0033 a0001c0001t0055 others(5): Show |
14 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1969G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1969 | chr7 | 22943620 | ||||||
chr7:22943777 | G | T | 1 | a0001c0001t0032 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1812C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1812 | chr7 | 22943777 | ||||||
chr7:22943981 | T | C | 26 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(23): Show |
77 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1608A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1608 | chr7 | 22943981 | ||||||
chr7:22944083 | A | T | 83 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(80): Show |
251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*1506T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1506 | chr7 | 22944083 | ||||||
chr7:22944161 | A | G | 1 | a0001c0001t0082 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1428T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1428 | chr7 | 22944161 | ||||||
chr7:22944235 | T | C | 10 | a0001c0001t0054 a0001c0002t0001 a0001c0002t0041 others(7): Show |
41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1354A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1354 | chr7 | 22944235 | ||||||
chr7:22944271 | T | C | 85 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(82): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1318A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1318 | chr7 | 22944271 | ||||||
chr7:22944281 | A | G | 1 | a0003c0003t0074 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1308 | chr7 | 22944281 | ||||||
chr7:22944341 | A | G | 1 | a0001c0002t0111 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1248 | chr7 | 22944341 | ||||||
chr7:22944731 | A | T | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*858T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 858 | chr7 | 22944731 | ||||||
chr7:22945006 | T | C | 1 | a0001c0001t0081 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 583 | chr7 | 22945006 | ||||||
chr7:22945137 | C | A | 1 | a0001c0001t0032 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*452G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 452 | chr7 | 22945137 | ||||||
chr7:22945152 | C | T | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 437 | chr7 | 22945152 | ||||||
chr7:22945153 | A | C | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*436T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 436 | chr7 | 22945153 | ||||||
chr7:22945154 | G | A | 55 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(52): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 435 | chr7 | 22945154 | ||||||
chr7:22945205 | T | C | 81 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(78): Show |
248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*384A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 384 | chr7 | 22945205 | ||||||
chr7:22945217 | C | G | 2 | a0001c0001t0058 a0001c0001t0059 |
2 | HG00639.hp1 HG00733.hp2 |
3_prime_UTR_variant | MODIFIER | c.*372G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 372 | chr7 | 22945217 | ||||||
chr7:22945348 | A | G | 19 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(16): Show |
70 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 241 | chr7 | 22945348 | ||||||
chr7:22945391 | A | C | 10 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0025 others(7): Show |
42 | HG00423.hp1 HG00544.hp2 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*198T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 198 | chr7 | 22945391 | ||||||
chr7:22945512 | G | C | 1 | a0001c0002t0111 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 77 | chr7 | 22945512 | ||||||
chr7:22945523 | C | T | 1 | a0001c0002t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 66 | chr7 | 22945523 | ||||||
chr7:23014007 | C | T | 1 | a0001c0001t0045 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22896 | chr7 | 23014007 | ||||||
chr7:23014059 | T | G | 1 | a0001c0002t0112 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22948 | chr7 | 23014059 | ||||||
chr7:23014078 | TCTCA | T | 3 | a0001c0001t0024 a0001c0001t0043 a0001c0001t0044 |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-186_-183delTGAG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22968 | chr7 | 23014078 | ||||||
chr7:23014098 | G | A | 1 | a0001c0001t0113 | 1 | NA19074.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-202C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | chr7 | 23014098 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22946174 | A | C | 5 | a0001c0001t0030g0077 a0001c0001t0030g0127 a0001c0001t0066g0128 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-11T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946174 | |||||||
chr7:22946249 | T | C | 59 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(56): Show |
78 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.992-86A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946249 | |||||||
chr7:22946332 | G | A | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.992-169C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946332 | |||||||
chr7:22946342 | C | G | 55 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(52): Show |
74 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.992-179G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946342 | |||||||
chr7:22946460 | T | C | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.992-297A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946460 | |||||||
chr7:22946488 | G | A | 30 | a0001c0002t0005g0018 a0001c0002t0005g0027 a0001c0002t0005g0033 others(27): Show |
33 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.992-325C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946488 | |||||||
chr7:22946498 | C | T | 6 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-335G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946498 | |||||||
chr7:22946748 | A | G | 1 | a0001c0001t0078g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.992-585T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946748 | |||||||
chr7:22946829 | A | G | 337 | a0001c0001t0002g0013 a0001c0001t0002g0065 a0001c0001t0002g0067 others(334): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.992-666T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946829 | |||||||
chr7:22946886 | T | C | 1 | a0001c0002t0041g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.992-723A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946886 | |||||||
chr7:22947160 | G | A | 1 | a0001c0002t0001g0277 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.992-997C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947160 | |||||||
chr7:22947171 | G | A | 1 | a0001c0002t0005g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.992-1008C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947171 | |||||||
chr7:22947511 | A | G | 1 | a0001c0002t0094g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.992-1348T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947511 | |||||||
chr7:22947741 | A | AGT | 218 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(215): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.992-1579_992-1578i others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947741 | |||||||
chr7:22947870 | A | G | 25 | a0001c0001t0007g0219 a0001c0002t0007g0005 a0001c0002t0007g0015 others(22): Show |
31 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.992-1707T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947870 | |||||||
chr7:22947881 | G | A | 166 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(163): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.992-1718C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947881 | |||||||
chr7:22948343 | T | C | 48 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(45): Show |
67 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.992-2180A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948343 | |||||||
chr7:22948608 | G | A | 1 | a0001c0002t0007g0204 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.992-2445C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948608 | |||||||
chr7:22948704 | G | C | 1 | a0001c0002t0098g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.992-2541C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948704 | |||||||
chr7:22948762 | A | G | 83 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(80): Show |
110 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.992-2599T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948762 | |||||||
chr7:22948969 | G | C | 150 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(147): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.992-2806C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948969 | |||||||
chr7:22949201 | A | G | 202 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(199): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.992-3038T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949201 | |||||||
chr7:22949224 | T | C | 1 | a0001c0002t0001g0274 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.992-3061A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949224 | |||||||
chr7:22949283 | A | G | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-3120T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949283 | |||||||
chr7:22949386 | A | G | 1 | a0001c0002t0007g0205 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.992-3223T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949386 | |||||||
chr7:22949469 | T | C | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.992-3306A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949469 | |||||||
chr7:22949521 | C | T | 49 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(46): Show |
68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.992-3358G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949521 | |||||||
chr7:22949522 | G | A | 1 | a0001c0001t0085g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.992-3359C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949522 | |||||||
chr7:22949585 | A | T | 213 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(210): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.992-3422T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949585 | |||||||
chr7:22949623 | G | A | 2 | a0001c0002t0007g0305 a0001c0002t0087g0209 |
2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.992-3460C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949623 | |||||||
chr7:22949722 | A | G | 2 | a0001c0001t0009g0148 a0001c0001t0064g0153 |
2 | HG00673.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.992-3559T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949722 | |||||||
chr7:22949800 | C | A | 2 | a0001c0002t0107g0269 a0001c0002t0108g0283 |
2 | NA18991.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.992-3637G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949800 | |||||||
chr7:22950027 | A | C | 9 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0075g0338 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.992-3864T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950027 | |||||||
chr7:22950141 | T | A | 2 | a0001c0001t0033g0050 a0001c0001t0077g0051 |
2 | HG01081.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.992-3978A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950141 | |||||||
chr7:22950257 | C | T | 1 | a0003c0003t0080g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.992-4094G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950257 | |||||||
chr7:22950339 | T | C | 12 | a0001c0002t0005g0018 a0001c0002t0005g0033 a0001c0002t0005g0231 others(9): Show |
13 | HG02040.hp2 HG02056.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.992-4176A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950339 | |||||||
chr7:22950365 | T | A | 55 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(52): Show |
74 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.992-4202A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950365 | |||||||
chr7:22950426 | T | C | 48 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(45): Show |
67 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.992-4263A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950426 | |||||||
chr7:22950654 | G | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.992-4491C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950654 | |||||||
chr7:22950840 | T | C | 1 | a0001c0001t0036g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.992-4677A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950840 | |||||||
chr7:22950989 | C | T | 5 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(2): Show |
8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.992-4826G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950989 | |||||||
chr7:22950996 | T | C | 1 | a0001c0001t0004g0325 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.992-4833A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950996 | |||||||
chr7:22951033 | A | G | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.992-4870T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951033 | |||||||
chr7:22951228 | C | T | 1 | a0001c0001t0009g0159 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.992-5065G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951228 | |||||||
chr7:22951356 | C | T | 1 | a0001c0001t0008g0309 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.992-5193G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951356 | |||||||
chr7:22951491 | A | G | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-5328T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951491 | |||||||
chr7:22951543 | T | A | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.992-5380A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951543 | |||||||
chr7:22951569 | C | CATAAA | 155 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(152): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.992-5407_992-5406i others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951569 | |||||||
chr7:22951783 | C | G | 1 | a0001c0001t0004g0025 | 2 | NA18966.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.992-5620G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951783 | |||||||
chr7:22952195 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.992-6032C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952195 | |||||||
chr7:22952263 | A | G | 153 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(150): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.992-6100T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952263 | |||||||
chr7:22952342 | T | C | 1 | a0001c0001t0016g0146 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.992-6179A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952342 | |||||||
chr7:22952366 | A | G | 103 | a0001c0001t0007g0219 a0001c0001t0054g0307 a0001c0002t0001g0001 others(100): Show |
120 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.992-6203T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952366 | |||||||
chr7:22952421 | C | T | 33 | a0001c0001t0054g0307 a0001c0002t0001g0001 a0001c0002t0001g0008 others(30): Show |
41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.992-6258G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952421 | |||||||
chr7:22952466 | G | A | 1 | a0001c0001t0066g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.992-6303C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952466 | |||||||
chr7:22952692 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.992-6529G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952692 | |||||||
chr7:22952909 | T | A | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.992-6746A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952909 | |||||||
chr7:22952999 | C | T | 151 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(148): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.992-6836G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952999 | |||||||
chr7:22953010 | A | G | 10 | a0001c0001t0008g0022 a0001c0001t0008g0309 a0001c0001t0008g0312 others(7): Show |
11 | HG01256.hp2 HG01516.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.992-6847T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953010 | |||||||
chr7:22953076 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-6913A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953076 | |||||||
chr7:22953168 | C | A | 151 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(148): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.992-7005G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953168 | |||||||
chr7:22953224 | G | A | 158 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(155): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.991+7032C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953224 | |||||||
chr7:22953338 | G | A | 33 | a0001c0001t0054g0307 a0001c0002t0001g0001 a0001c0002t0001g0008 others(30): Show |
41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.991+6918C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953338 | |||||||
chr7:22953349 | T | C | 4 | a0001c0002t0010g0020 a0001c0002t0010g0260 a0001c0002t0022g0261 others(1): Show |
5 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+6907A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953349 | |||||||
chr7:22953509 | C | T | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991+6747G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953509 | |||||||
chr7:22953714 | T | C | 151 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(148): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.991+6542A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953714 | |||||||
chr7:22953864 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991+6392G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953864 | |||||||
chr7:22953874 | T | A | 131 | a0001c0001t0007g0219 a0001c0001t0054g0307 a0001c0002t0001g0001 others(128): Show |
149 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.991+6382A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953874 | |||||||
chr7:22953885 | A | T | 131 | a0001c0001t0007g0219 a0001c0001t0054g0307 a0001c0002t0001g0001 others(128): Show |
149 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.991+6371T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953885 | |||||||
chr7:22954136 | G | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+6120C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954136 | |||||||
chr7:22954155 | C | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+6101G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954155 | |||||||
chr7:22954322 | A | T | 8 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0076g0054 others(5): Show |
8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+5934T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954322 | |||||||
chr7:22954348 | T | G | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.991+5908A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954348 | |||||||
chr7:22954458 | T | C | 5 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(2): Show |
8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+5798A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954458 | |||||||
chr7:22954486 | A | T | 1 | a0001c0002t0007g0218 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.991+5770T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954486 | |||||||
chr7:22954567 | T | G | 1 | a0001c0002t0005g0027 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.991+5689A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954567 | |||||||
chr7:22954715 | CATT | C | 151 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(148): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.991+5538_991+5540d others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954715 | |||||||
chr7:22954771 | T | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991+5485A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954771 | |||||||
chr7:22954811 | AATTAAAT others(173): Show |
A | 1 | a0001c0002t0010g0293 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.991+5265_991+5444d others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954811 | |||||||
chr7:22955138 | C | T | 1 | a0001c0001t0004g0328 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.991+5118G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955138 | |||||||
chr7:22955261 | T | C | 1 | a0001c0002t0099g0216 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.991+4995A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955261 | |||||||
chr7:22955300 | T | C | 160 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(157): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.991+4956A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955300 | |||||||
chr7:22955335 | T | C | 33 | a0001c0001t0054g0307 a0001c0002t0001g0001 a0001c0002t0001g0008 others(30): Show |
41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.991+4921A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955335 | |||||||
chr7:22955337 | C | CTTAA | 153 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(150): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.991+4915_991+4918d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955337 | |||||||
chr7:22955358 | A | G | 1 | a0001c0001t0004g0310 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.991+4898T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955358 | |||||||
chr7:22955420 | C | G | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+4836G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955420 | |||||||
chr7:22955565 | CA | C | 3 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0001t0072g0329 |
3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.991+4690delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955565 | |||||||
chr7:22955859 | C | T | 1 | a0001c0001t0003g0096 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.991+4397G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955859 | |||||||
chr7:22955907 | A | G | 4 | a0001c0001t0006g0164 a0001c0001t0006g0170 a0001c0001t0009g0145 others(1): Show |
4 | NA18978.hp1 NA19009.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+4349T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955907 | |||||||
chr7:22956094 | T | C | 1 | a0001c0001t0004g0317 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.991+4162A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956094 | |||||||
chr7:22956111 | C | T | 157 | a0001c0001t0007g0219 a0001c0001t0013g0072 a0001c0001t0013g0122 others(154): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.991+4145G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956111 | |||||||
chr7:22956219 | C | T | 6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+4037G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956219 | |||||||
chr7:22956327 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.991+3929C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956327 | |||||||
chr7:22956447 | ATTAAG | A | 8 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0076g0054 others(5): Show |
8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+3804_991+3808d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956447 | |||||||
chr7:22956464 | C | T | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.991+3792G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956464 | |||||||
chr7:22956541 | CA | C | 149 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(146): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.991+3714delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956541 | |||||||
chr7:22956814 | A | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+3442T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956814 | |||||||
chr7:22956892 | T | A | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+3364A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956892 | |||||||
chr7:22957013 | G | A | 2 | a0001c0002t0012g0189 a0001c0002t0012g0190 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.991+3243C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957013 | |||||||
chr7:22957042 | T | A | 1 | a0001c0002t0090g0287 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.991+3214A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957042 | |||||||
chr7:22957064 | G | A | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+3192C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957064 | |||||||
chr7:22957174 | A | G | 337 | a0001c0001t0002g0013 a0001c0001t0002g0065 a0001c0001t0002g0067 others(334): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.991+3082T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957174 | |||||||
chr7:22957197 | T | C | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+3059A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957197 | |||||||
chr7:22957206 | C | T | 15 | a0001c0001t0003g0007 a0001c0001t0003g0139 a0001c0001t0003g0143 others(12): Show |
17 | HG02015.hp2 HG02056.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.991+3050G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957206 | |||||||
chr7:22957302 | GA | G | 335 | a0001c0001t0002g0013 a0001c0001t0002g0065 a0001c0001t0002g0067 others(332): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.991+2953delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957302 | |||||||
chr7:22957476 | A | G | 1 | a0001c0001t0093g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.991+2780T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957476 | |||||||
chr7:22957493 | A | G | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+2763T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957493 | |||||||
chr7:22957545 | G | A | 164 | a0001c0001t0007g0219 a0001c0001t0013g0061 a0001c0001t0013g0072 others(161): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.991+2711C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957545 | |||||||
chr7:22957690 | T | C | 1 | a0001c0001t0008g0319 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.991+2566A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957690 | |||||||
chr7:22957820 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.991+2436C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957820 | |||||||
chr7:22957829 | T | C | 6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+2427A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957829 | |||||||
chr7:22957842 | TGA | T | 6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+2412_991+2413d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957842 | |||||||
chr7:22957986 | A | C | 2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.991+2270T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957986 | |||||||
chr7:22957990 | T | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.991+2266A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957990 | |||||||
chr7:22958023 | C | A | 47 | a0001c0002t0005g0018 a0001c0002t0005g0027 a0001c0002t0005g0033 others(44): Show |
50 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.991+2233G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958023 | |||||||
chr7:22958329 | G | T | 51 | a0001c0001t0002g0149 a0001c0001t0002g0182 a0001c0001t0003g0007 others(48): Show |
57 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.991+1927C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958329 | |||||||
chr7:22958523 | G | A | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.991+1733C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958523 | |||||||
chr7:22958716 | G | A | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.991+1540C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958716 | |||||||
chr7:22958771 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.991+1485C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958771 | |||||||
chr7:22958855 | G | A | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.991+1401C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958855 | |||||||
chr7:22959014 | A | G | 1 | a0001c0002t0102g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.991+1242T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959014 | |||||||
chr7:22959015 | T | C | 6 | a0001c0001t0002g0202 a0001c0001t0002g0336 a0001c0001t0003g0089 others(3): Show |
6 | HG00438.hp2 HG01106.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.991+1241A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959015 | |||||||
chr7:22959192 | T | G | 1 | a0001c0002t0005g0033 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.991+1064A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959192 | |||||||
chr7:22959261 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+995A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959261 | |||||||
chr7:22959268 | C | T | 194 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(191): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.991+988G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959268 | |||||||
chr7:22959291 | G | A | 147 | a0001c0001t0013g0061 a0001c0001t0013g0072 a0001c0001t0013g0122 others(144): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.991+965C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959291 | |||||||
chr7:22959357 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.991+899A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959357 | |||||||
chr7:22959453 | T | C | 4 | a0001c0002t0010g0227 a0001c0002t0022g0296 a0001c0002t0083g0288 others(1): Show |
4 | HG01192.hp1 HG01257.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.991+803A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959453 | |||||||
chr7:22959588 | A | G | 79 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(76): Show |
90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.991+668T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959588 | |||||||
chr7:22959649 | T | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.991+607A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959649 | |||||||
chr7:22959649 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.991+607A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959649 | |||||||
chr7:22959764 | C | A | 7 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0037g0034 others(4): Show |
7 | HG01361.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+492G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959764 | |||||||
chr7:22960002 | T | C | 1 | a0001c0002t0001g0275 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.991+254A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22960002 | |||||||
chr7:22960457 | A | AAGATCAA others(3): Show |
4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-43_832-42insAT others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960457 | |||||||
chr7:22960483 | G | A | 1 | a0001c0001t0006g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.832-68C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960483 | |||||||
chr7:22960515 | A | C | 3 | a0001c0001t0014g0108 a0001c0001t0014g0114 a0001c0001t0082g0131 |
3 | HG03239.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.832-100T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960515 | |||||||
chr7:22960572 | G | A | 1 | a0001c0001t0011g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.832-157C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960572 | |||||||
chr7:22960787 | C | T | 1 | a0001c0001t0050g0306 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.832-372G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960787 | |||||||
chr7:22961042 | A | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831+193T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961042 | |||||||
chr7:22961062 | T | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+173A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961062 | |||||||
chr7:22961064 | A | T | 2 | a0001c0002t0005g0242 a0001c0002t0102g0241 |
2 | HG02040.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.831+171T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961064 | |||||||
chr7:22961081 | A | G | 1 | a0001c0002t0098g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.831+154T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961081 | |||||||
chr7:22961164 | G | GCTCT | 224 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(221): Show |
262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.831+67_831+70dupAG others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961164 | |||||||
chr7:22961767 | T | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-445A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961767 | |||||||
chr7:22961869 | G | C | 1 | a0001c0001t0003g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.744-547C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961869 | |||||||
chr7:22961969 | T | A | 1 | a0001c0001t0002g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.744-647A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961969 | |||||||
chr7:22962025 | C | G | 1 | a0001c0001t0069g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.744-703G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962025 | |||||||
chr7:22962034 | T | C | 32 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(29): Show |
40 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.744-712A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962034 | |||||||
chr7:22962076 | G | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0133 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.744-754C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962076 | |||||||
chr7:22962078 | T | G | 1 | a0001c0002t0098g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.744-756A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962078 | |||||||
chr7:22962081 | TC | T | 148 | a0001c0001t0013g0072 a0001c0001t0013g0122 a0001c0001t0013g0134 others(145): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-760delG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962081 | |||||||
chr7:22962188 | C | T | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-866G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962188 | |||||||
chr7:22962204 | T | G | 2 | a0001c0001t0014g0084 a0001c0001t0014g0111 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.744-882A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962204 | |||||||
chr7:22962235 | T | A | 4 | a0001c0002t0001g0008 a0001c0002t0001g0232 a0001c0002t0001g0286 others(1): Show |
6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-913A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962235 | |||||||
chr7:22962248 | A | G | 1 | a0001c0001t0028g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.744-926T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962248 | |||||||
chr7:22962288 | G | A | 4 | a0001c0002t0001g0008 a0001c0002t0001g0232 a0001c0002t0001g0286 others(1): Show |
6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-966C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962288 | |||||||
chr7:22962537 | C | T | 32 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(29): Show |
40 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.744-1215G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962537 | |||||||
chr7:22962545 | A | T | 161 | a0001c0001t0013g0072 a0001c0001t0013g0122 a0001c0001t0013g0134 others(158): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.744-1223T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962545 | |||||||
chr7:22962564 | G | A | 3 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 |
3 | HG01361.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.744-1242C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962564 | |||||||
chr7:22962578 | G | GA | 148 | a0001c0001t0009g0145 a0001c0001t0009g0155 a0001c0001t0013g0072 others(145): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-1257dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962578 | |||||||
chr7:22962735 | C | T | 47 | a0001c0002t0005g0018 a0001c0002t0005g0027 a0001c0002t0005g0033 others(44): Show |
50 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.744-1413G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962735 | |||||||
chr7:22962741 | C | A | 3 | a0001c0001t0002g0081 a0001c0001t0002g0087 a0001c0001t0003g0096 |
3 | NA18956.hp2 NA18981.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.744-1419G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962741 | |||||||
chr7:22962754 | T | C | 150 | a0001c0001t0013g0061 a0001c0001t0013g0072 a0001c0001t0013g0122 others(147): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.744-1432A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962754 | |||||||
chr7:22962757 | C | A | 147 | a0001c0001t0013g0072 a0001c0001t0013g0122 a0001c0001t0013g0134 others(144): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.744-1435G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962757 | |||||||
chr7:22962779 | G | T | 38 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(35): Show |
54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.744-1457C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962779 | |||||||
chr7:22962805 | C | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.744-1483G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962805 | |||||||
chr7:22962874 | C | T | 148 | a0001c0001t0013g0072 a0001c0001t0013g0122 a0001c0001t0013g0134 others(145): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.743+1541G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962874 | |||||||
chr7:22962960 | A | C | 1 | a0001c0002t0010g0293 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.743+1455T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962960 | |||||||
chr7:22963138 | C | A | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.743+1277G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963138 | |||||||
chr7:22963154 | C | A | 3 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0001t0056g0044 |
3 | HG02109.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+1261G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963154 | |||||||
chr7:22963170 | C | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.743+1245G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963170 | |||||||
chr7:22963171 | A | G | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.743+1244T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963171 | |||||||
chr7:22963401 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743+1014G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963401 | |||||||
chr7:22963409 | G | A | 1 | a0001c0001t0003g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.743+1006C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963409 | |||||||
chr7:22963487 | T | C | 11 | a0001c0002t0001g0001 a0001c0002t0001g0223 a0001c0002t0001g0266 others(8): Show |
16 | NA18946.hp1 NA18954.hp1 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+928A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963487 | |||||||
chr7:22963503 | C | T | 1 | a0001c0002t0010g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.743+912G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963503 | |||||||
chr7:22963646 | C | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.743+769G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963646 | |||||||
chr7:22963647 | G | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+768C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963647 | |||||||
chr7:22963719 | A | G | 22 | a0001c0001t0013g0061 a0001c0001t0013g0072 a0001c0001t0013g0122 others(19): Show |
22 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.743+696T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963719 | |||||||
chr7:22963869 | T | C | 1 | a0001c0002t0042g0278 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.743+546A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963869 | |||||||
chr7:22964109 | C | CA | 104 | a0001c0001t0003g0080 a0001c0001t0009g0155 a0001c0002t0001g0001 others(101): Show |
121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.743+305dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22964109 | |||||||
chr7:22964395 | G | A | 2 | a0003c0003t0074g0053 a0003c0003t0080g0052 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.743+20C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22964395 | |||||||
chr7:22964754 | A | G | 205 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(202): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.627-223T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964754 | |||||||
chr7:22964768 | C | A | 1 | a0001c0001t0063g0151 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.627-237G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964768 | |||||||
chr7:22964783 | G | A | 159 | a0001c0001t0013g0061 a0001c0001t0013g0072 a0001c0001t0013g0122 others(156): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.627-252C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964783 | |||||||
chr7:22964834 | C | T | 3 | a0001c0002t0007g0210 a0001c0002t0007g0215 a0001c0002t0100g0206 |
3 | HG02004.hp1 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.627-303G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964834 | |||||||
chr7:22964895 | G | A | 2 | a0001c0001t0075g0338 a0001c0001t0078g0056 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.627-364C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964895 | |||||||
chr7:22965012 | T | C | 1 | a0001c0001t0027g0014 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.627-481A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965012 | |||||||
chr7:22965129 | A | AT | 8 | a0001c0001t0006g0082 a0001c0001t0009g0092 a0001c0001t0017g0085 others(5): Show |
8 | NA18942.hp2 NA18965.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-599dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965129 | |||||||
chr7:22965131 | TA | T | 192 | a0001c0001t0003g0080 a0001c0001t0004g0006 a0001c0001t0004g0009 others(189): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.627-601delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965131 | |||||||
chr7:22965144 | A | G | 5 | a0001c0002t0007g0005 a0001c0002t0007g0015 a0001c0002t0007g0207 others(2): Show |
7 | NA18956.hp1 NA18960.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-613T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965144 | |||||||
chr7:22965219 | T | G | 2 | a0001c0001t0026g0311 a0001c0001t0026g0321 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.627-688A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965219 | |||||||
chr7:22965421 | A | G | 1 | a0001c0001t0079g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.627-890T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965421 | |||||||
chr7:22965431 | G | T | 3 | a0001c0001t0004g0024 a0001c0001t0004g0048 a0001c0001t0053g0323 |
4 | HG01928.hp1 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-900C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965431 | |||||||
chr7:22965457 | C | T | 22 | a0001c0002t0007g0005 a0001c0002t0007g0015 a0001c0002t0007g0204 others(19): Show |
28 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(25): Show |
intron_variant | MODIFIER | c.627-926G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965457 | |||||||
chr7:22965483 | T | G | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-952A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965483 | |||||||
chr7:22965528 | C | T | 4 | a0001c0001t0019g0117 a0001c0001t0019g0333 a0001c0001t0019g0334 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-997G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965528 | |||||||
chr7:22965594 | T | TA | 36 | a0001c0001t0004g0009 a0001c0001t0004g0324 a0001c0001t0008g0318 others(33): Show |
44 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.627-1064dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965594 | |||||||
chr7:22965594 | TA | T | 6 | a0001c0001t0006g0082 a0001c0001t0019g0117 a0001c0001t0028g0152 others(3): Show |
6 | HG01069.hp2 NA18942.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.627-1064delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965594 | |||||||
chr7:22965606 | A | C | 2 | a0001c0001t0002g0073 a0001c0001t0002g0133 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.627-1075T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965606 | |||||||
chr7:22965746 | C | T | 2 | a0001c0001t0075g0338 a0001c0001t0078g0056 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.627-1215G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965746 | |||||||
chr7:22965881 | G | A | 1 | a0001c0001t0016g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627-1350C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965881 | |||||||
chr7:22966217 | A | G | 1 | a0001c0001t0011g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.627-1686T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966217 | |||||||
chr7:22966301 | T | C | 2 | a0001c0001t0002g0073 a0001c0001t0002g0133 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.627-1770A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966301 | |||||||
chr7:22966339 | T | C | 44 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(41): Show |
60 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.627-1808A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966339 | |||||||
chr7:22966364 | T | C | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627-1833A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966364 | |||||||
chr7:22966471 | T | C | 24 | a0001c0002t0007g0005 a0001c0002t0007g0015 a0001c0002t0007g0204 others(21): Show |
30 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(27): Show |
intron_variant | MODIFIER | c.627-1940A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966471 | |||||||
chr7:22966534 | T | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.627-2003A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966534 | |||||||
chr7:22966615 | T | C | 1 | a0001c0002t0112g0340 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.627-2084A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966615 | |||||||
chr7:22966633 | T | A | 1 | a0001c0002t0023g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.627-2102A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966633 | |||||||
chr7:22966674 | A | G | 1 | a0001c0002t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.627-2143T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966674 | |||||||
chr7:22966686 | T | C | 1 | a0001c0002t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.627-2155A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966686 | |||||||
chr7:22966933 | A | G | 5 | a0001c0001t0002g0202 a0001c0001t0002g0336 a0001c0001t0003g0089 others(2): Show |
5 | HG01106.hp2 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-2402T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966933 | |||||||
chr7:22967035 | G | A | 2 | a0001c0001t0003g0163 a0001c0001t0006g0162 |
2 | HG02056.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.627-2504C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967035 | |||||||
chr7:22967051 | T | C | 1 | a0001c0001t0020g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627-2520A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967051 | |||||||
chr7:22967276 | G | A | 3 | a0001c0001t0075g0338 a0001c0001t0078g0056 a0001c0001t0082g0131 |
3 | HG02622.hp2 HG02630.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.627-2745C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967276 | |||||||
chr7:22967537 | G | A | 37 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(34): Show |
53 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.627-3006C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967537 | |||||||
chr7:22967588 | T | C | 9 | a0001c0002t0010g0020 a0001c0002t0010g0227 a0001c0002t0010g0260 others(6): Show |
10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.627-3057A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967588 | |||||||
chr7:22967594 | T | G | 39 | a0001c0001t0006g0164 a0001c0001t0006g0170 a0001c0001t0009g0140 others(36): Show |
47 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.627-3063A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967594 | |||||||
chr7:22967612 | G | A | 3 | a0001c0002t0010g0020 a0001c0002t0010g0260 a0001c0002t0022g0261 |
4 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-3081C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967612 | |||||||
chr7:22967710 | G | A | 2 | a0001c0001t0014g0108 a0001c0001t0014g0114 |
2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.627-3179C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967710 | |||||||
chr7:22967897 | C | T | 3 | a0001c0001t0079g0055 a0003c0003t0074g0053 a0003c0003t0080g0052 |
3 | HG02145.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627-3366G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967897 | |||||||
chr7:22967898 | G | A | 1 | a0001c0001t0016g0147 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-3367C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967898 | |||||||
chr7:22967934 | C | G | 3 | a0001c0002t0021g0230 a0001c0002t0034g0226 a0001c0002t0034g0299 |
3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.627-3403G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967934 | |||||||
chr7:22968080 | A | G | 9 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0075g0338 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-3549T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968080 | |||||||
chr7:22968365 | C | T | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-3834G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968365 | |||||||
chr7:22968371 | A | T | 49 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(46): Show |
68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.627-3840T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968371 | |||||||
chr7:22968420 | T | C | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.627-3889A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968420 | |||||||
chr7:22968566 | A | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.627-4035T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968566 | |||||||
chr7:22968576 | T | C | 5 | a0001c0001t0030g0077 a0001c0001t0030g0127 a0001c0001t0066g0128 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-4045A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968576 | |||||||
chr7:22968589 | T | C | 201 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(198): Show |
238 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.627-4058A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968589 | |||||||
chr7:22968598 | A | C | 1 | a0001c0001t0063g0151 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.627-4067T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968598 | |||||||
chr7:22968604 | G | A | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627-4073C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968604 | |||||||
chr7:22968698 | C | T | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.627-4167G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968698 | |||||||
chr7:22968704 | A | G | 1 | a0001c0001t0008g0309 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.627-4173T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968704 | |||||||
chr7:22968751 | G | A | 1 | a0001c0001t0009g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.627-4220C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968751 | |||||||
chr7:22968837 | T | C | 134 | a0001c0001t0006g0164 a0001c0001t0006g0170 a0001c0001t0009g0140 others(131): Show |
152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-4306A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968837 | |||||||
chr7:22968901 | G | A | 1 | a0001c0002t0005g0238 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.627-4370C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968901 | |||||||
chr7:22968985 | C | T | 1 | a0001c0002t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.627-4454G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968985 | |||||||
chr7:22969197 | T | C | 2 | a0001c0002t0005g0248 a0001c0002t0103g0254 |
2 | NA18987.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.627-4666A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969197 | |||||||
chr7:22969305 | G | A | 134 | a0001c0001t0006g0164 a0001c0001t0006g0170 a0001c0001t0009g0140 others(131): Show |
152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-4774C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969305 | |||||||
chr7:22969318 | T | TTG | 11 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0075g0338 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.627-4789_627-4788d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969318 | |||||||
chr7:22969448 | G | A | 7 | a0001c0001t0003g0168 a0001c0001t0003g0331 a0001c0001t0003g0332 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-4917C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969448 | |||||||
chr7:22969471 | G | C | 1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627-4940C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969471 | |||||||
chr7:22969507 | T | C | 1 | a0001c0002t0005g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.627-4976A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969507 | |||||||
chr7:22969524 | G | T | 3 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0001t0072g0329 |
3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.627-4993C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969524 | |||||||
chr7:22969525 | G | GT | 8 | a0001c0001t0002g0106 a0001c0001t0002g0149 a0001c0001t0003g0089 others(5): Show |
8 | HG00438.hp2 HG01516.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.627-4995dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969525 | |||||||
chr7:22969525 | GT | G | 188 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(185): Show |
225 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.627-4995delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969525 | |||||||
chr7:22969526 | T | G | 4 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0001t0072g0329 others(1): Show |
4 | HG02896.hp2 NA18522.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-4995A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969526 | |||||||
chr7:22970012 | T | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.627-5481A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970012 | |||||||
chr7:22970111 | C | CACATGAA others(82): Show |
6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-5669_627-5581d others(91): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970111 | |||||||
chr7:22970135 | T | C | 6 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-5604A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970135 | |||||||
chr7:22970196 | A | G | 1 | a0001c0002t0012g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.627-5665T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970196 | |||||||
chr7:22970276 | T | C | 134 | a0001c0001t0006g0164 a0001c0001t0006g0170 a0001c0001t0009g0140 others(131): Show |
152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-5745A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970276 | |||||||
chr7:22970342 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-5811A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970342 | |||||||
chr7:22970444 | T | C | 172 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(169): Show |
206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.626+5766A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970444 | |||||||
chr7:22970457 | A | G | 1 | a0001c0001t0008g0023 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.626+5753T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970457 | |||||||
chr7:22970525 | C | CA | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5684dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970525 | |||||||
chr7:22970806 | C | T | 2 | a0003c0003t0074g0053 a0003c0003t0080g0052 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.626+5404G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970806 | |||||||
chr7:22970837 | C | T | 1 | a0001c0002t0087g0209 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.626+5373G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970837 | |||||||
chr7:22970859 | G | A | 1 | a0001c0002t0010g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.626+5351C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970859 | |||||||
chr7:22970926 | T | C | 79 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(76): Show |
90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.626+5284A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970926 | |||||||
chr7:22971135 | T | C | 1 | a0001c0001t0013g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.626+5075A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971135 | |||||||
chr7:22971210 | C | T | 1 | a0001c0001t0093g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.626+5000G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971210 | |||||||
chr7:22971217 | G | A | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.626+4993C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971217 | |||||||
chr7:22971225 | C | T | 4 | a0001c0001t0019g0117 a0001c0001t0019g0333 a0001c0001t0019g0334 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+4985G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971225 | |||||||
chr7:22971418 | A | G | 172 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(169): Show |
206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.626+4792T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971418 | |||||||
chr7:22971573 | C | T | 1 | a0001c0002t0097g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.626+4637G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971573 | |||||||
chr7:22971598 | C | T | 3 | a0001c0002t0035g0059 a0001c0002t0046g0038 a0001c0002t0091g0058 |
3 | HG02055.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.626+4612G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971598 | |||||||
chr7:22971638 | T | C | 15 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(12): Show |
18 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.626+4572A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971638 | |||||||
chr7:22971657 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.626+4553G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971657 | |||||||
chr7:22971677 | C | CA | 6 | a0001c0001t0014g0108 a0001c0001t0014g0114 a0001c0001t0032g0303 others(3): Show |
6 | HG01978.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+4532dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971677 | |||||||
chr7:22971677 | CA | C | 171 | a0001c0001t0002g0067 a0001c0001t0002g0074 a0001c0001t0003g0139 others(168): Show |
205 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.626+4532delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971677 | |||||||
chr7:22971803 | G | A | 128 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(125): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.626+4407C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971803 | |||||||
chr7:22971843 | C | T | 41 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(38): Show |
57 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.626+4367G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971843 | |||||||
chr7:22971954 | G | A | 2 | a0001c0001t0006g0154 a0001c0001t0009g0155 |
2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.626+4256C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971954 | |||||||
chr7:22972006 | G | C | 4 | a0001c0001t0017g0085 a0001c0001t0017g0098 a0001c0001t0017g0130 others(1): Show |
4 | NA18942.hp2 NA18984.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+4204C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972006 | |||||||
chr7:22972036 | A | G | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.626+4174T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972036 | |||||||
chr7:22972057 | A | T | 1 | a0001c0002t0005g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.626+4153T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972057 | |||||||
chr7:22972153 | T | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.626+4057A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972153 | |||||||
chr7:22972238 | GC | G | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+3971delG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972238 | |||||||
chr7:22972312 | A | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.626+3898T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972312 | |||||||
chr7:22972720 | T | A | 1 | a0001c0002t0007g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+3490A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972720 | |||||||
chr7:22972796 | C | T | 2 | a0001c0002t0007g0207 a0001c0002t0007g0208 |
2 | NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.626+3414G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972796 | |||||||
chr7:22972885 | G | T | 12 | a0001c0002t0012g0189 a0001c0002t0012g0190 a0001c0002t0012g0192 others(9): Show |
12 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+3325C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972885 | |||||||
chr7:22972960 | C | G | 1 | a0001c0001t0003g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.626+3250G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972960 | |||||||
chr7:22972976 | T | C | 2 | a0001c0001t0026g0311 a0001c0001t0026g0321 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+3234A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972976 | |||||||
chr7:22973143 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+3067A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973143 | |||||||
chr7:22973259 | C | A | 1 | a0001c0001t0067g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.626+2951G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973259 | |||||||
chr7:22973354 | A | G | 4 | a0001c0001t0076g0054 a0001c0001t0079g0055 a0003c0003t0074g0053 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+2856T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973354 | |||||||
chr7:22973452 | A | G | 3 | a0001c0002t0021g0230 a0001c0002t0034g0226 a0001c0002t0034g0299 |
3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.626+2758T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973452 | |||||||
chr7:22973499 | T | C | 1 | a0001c0001t0070g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.626+2711A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973499 | |||||||
chr7:22973617 | C | T | 194 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(191): Show |
231 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.626+2593G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973617 | |||||||
chr7:22973758 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.626+2452A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973758 | |||||||
chr7:22973799 | T | G | 1 | a0004c0004t0029g0012 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.626+2411A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973799 | |||||||
chr7:22974066 | T | C | 172 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(169): Show |
206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.626+2144A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974066 | |||||||
chr7:22974229 | C | T | 172 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(169): Show |
206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.626+1981G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974229 | |||||||
chr7:22974736 | C | T | 6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.626+1474G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974736 | |||||||
chr7:22974791 | C | T | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.626+1419G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974791 | |||||||
chr7:22974828 | G | C | 26 | a0001c0002t0001g0008 a0001c0002t0001g0232 a0001c0002t0001g0286 others(23): Show |
34 | HG00140.hp1 HG01070.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.626+1382C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974828 | |||||||
chr7:22974905 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+1305A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974905 | |||||||
chr7:22974931 | C | T | 1 | a0001c0001t0009g0156 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+1279G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974931 | |||||||
chr7:22975197 | T | A | 48 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(45): Show |
67 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.626+1013A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975197 | |||||||
chr7:22975201 | TTTTG | T | 128 | a0001c0001t0081g0188 a0001c0002t0001g0001 a0001c0002t0001g0008 others(125): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.626+1005_626+1008d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975201 | |||||||
chr7:22975378 | A | G | 1 | a0001c0002t0005g0255 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.626+832T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975378 | |||||||
chr7:22975810 | G | A | 2 | a0001c0001t0075g0338 a0001c0001t0078g0056 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.626+400C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975810 | |||||||
chr7:22975862 | G | A | 45 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(42): Show |
64 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.626+348C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975862 | |||||||
chr7:22975896 | T | C | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.626+314A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975896 | |||||||
chr7:22975955 | C | T | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.626+255G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975955 | |||||||
chr7:22975974 | G | A | 44 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(41): Show |
63 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.626+236C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975974 | |||||||
chr7:22976063 | A | G | 1 | a0001c0002t0005g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.626+147T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22976063 | |||||||
chr7:22976170 | C | T | 1 | a0001c0001t0006g0144 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.626+40G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22976170 | |||||||
chr7:22976340 | T | C | 2 | a0001c0001t0013g0061 a0007c0007t0013g0060 |
2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.531-35A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976340 | |||||||
chr7:22976418 | A | G | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.531-113T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976418 | |||||||
chr7:22976496 | T | G | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531-191A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976496 | |||||||
chr7:22976548 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.530+145C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976548 | |||||||
chr7:22976665 | G | C | 2 | a0001c0001t0031g0099 a0001c0001t0031g0102 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.530+28C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976665 | |||||||
chr7:22976911 | A | G | 129 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.415-103T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22976911 | |||||||
chr7:22977028 | T | C | 129 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.415-220A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977028 | |||||||
chr7:22977074 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.415-266T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977074 | |||||||
chr7:22977268 | A | G | 1 | a0001c0002t0022g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.414+73T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977268 | |||||||
chr7:22977322 | G | A | 14 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0033g0049 others(11): Show |
14 | HG01081.hp2 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+19C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977322 | |||||||
chr7:22977572 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.334-151A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977572 | |||||||
chr7:22977599 | T | C | 2 | a0001c0002t0005g0237 a0001c0002t0005g0249 |
2 | HG02165.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.334-178A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977599 | |||||||
chr7:22977848 | T | C | 9 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0075g0338 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+421A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977848 | |||||||
chr7:22977950 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.333+319G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977950 | |||||||
chr7:22978477 | G | T | 2 | a0001c0001t0019g0117 a0001c0001t0061g0118 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154-29C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978477 | |||||||
chr7:22978602 | C | G | 1 | a0001c0001t0085g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.154-154G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978602 | |||||||
chr7:22978604 | T | C | 1 | a0001c0001t0008g0319 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.154-156A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978604 | |||||||
chr7:22978699 | G | A | 7 | a0001c0001t0003g0168 a0001c0001t0003g0331 a0001c0001t0003g0332 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-251C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978699 | |||||||
chr7:22979014 | G | A | 4 | a0001c0001t0019g0117 a0001c0001t0019g0333 a0001c0001t0019g0334 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-566C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979014 | |||||||
chr7:22979096 | C | T | 1 | a0001c0001t0016g0147 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154-648G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979096 | |||||||
chr7:22979182 | G | T | 1 | a0001c0002t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.154-734C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979182 | |||||||
chr7:22979278 | G | C | 1 | a0001c0002t0001g0001 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154-830C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979278 | |||||||
chr7:22979418 | T | C | 1 | a0001c0001t0060g0141 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.154-970A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979418 | |||||||
chr7:22979506 | G | A | 20 | a0001c0001t0013g0072 a0001c0001t0013g0122 a0001c0001t0013g0134 others(17): Show |
20 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-1058C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979506 | |||||||
chr7:22979587 | C | T | 136 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0037g0034 others(133): Show |
154 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.154-1139G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979587 | |||||||
chr7:22979771 | A | G | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.154-1323T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979771 | |||||||
chr7:22979782 | G | C | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.154-1334C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979782 | |||||||
chr7:22979792 | C | T | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-1344G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979792 | |||||||
chr7:22979804 | C | G | 21 | a0001c0002t0007g0005 a0001c0002t0007g0015 a0001c0002t0007g0204 others(18): Show |
27 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-1356G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979804 | |||||||
chr7:22979828 | G | A | 1 | a0001c0001t0017g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.154-1380C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979828 | |||||||
chr7:22979977 | T | A | 1 | a0001c0001t0004g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.154-1529A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979977 | |||||||
chr7:22980006 | T | G | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.154-1558A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980006 | |||||||
chr7:22980158 | T | C | 2 | a0001c0001t0032g0303 a0001c0001t0032g0304 |
2 | NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.154-1710A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980158 | |||||||
chr7:22980191 | A | G | 129 | a0001c0001t0043g0028 a0001c0002t0001g0001 a0001c0002t0001g0008 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.154-1743T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980191 | |||||||
chr7:22980274 | G | GT | 15 | a0001c0001t0013g0142 a0001c0001t0014g0108 a0001c0001t0014g0114 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.154-1827dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | |||||||
chr7:22980274 | G | GTT | 124 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(121): Show |
141 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.154-1828_154-1827d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | |||||||
chr7:22980274 | GT | G | 14 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0069 others(11): Show |
14 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.154-1827delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | |||||||
chr7:22980314 | T | C | 1 | a0001c0001t0008g0320 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.154-1866A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980314 | |||||||
chr7:22980677 | G | A | 1 | a0001c0001t0085g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.154-2229C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980677 | |||||||
chr7:22980692 | C | T | 2 | a0001c0001t0075g0338 a0008c0009t0073g0337 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.154-2244G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980692 | |||||||
chr7:22980890 | G | A | 1 | a0001c0001t0004g0325 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.154-2442C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980890 | |||||||
chr7:22980894 | C | T | 331 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0069 others(328): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.154-2446G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980894 | |||||||
chr7:22980939 | T | A | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.154-2491A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980939 | |||||||
chr7:22980953 | C | A | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154-2505G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980953 | |||||||
chr7:22981053 | G | A | 127 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(124): Show |
145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.154-2605C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981053 | |||||||
chr7:22981090 | T | G | 1 | a0001c0002t0007g0214 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.154-2642A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981090 | |||||||
chr7:22981176 | A | C | 9 | a0001c0002t0010g0020 a0001c0002t0010g0227 a0001c0002t0010g0260 others(6): Show |
10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.154-2728T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981176 | |||||||
chr7:22981258 | C | T | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0136 |
3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.153+2686G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981258 | |||||||
chr7:22981369 | A | G | 127 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(124): Show |
145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.153+2575T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981369 | |||||||
chr7:22981463 | A | C | 190 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(187): Show |
227 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.153+2481T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981463 | |||||||
chr7:22981519 | A | C | 1 | a0001c0002t0012g0192 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+2425T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981519 | |||||||
chr7:22981582 | A | C | 2 | a0001c0002t0001g0008 a0001c0002t0001g0232 |
4 | HG00140.hp1 HG01070.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+2362T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981582 | |||||||
chr7:22981773 | C | T | 1 | a0001c0002t0103g0254 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.153+2171G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981773 | |||||||
chr7:22981836 | T | C | 54 | a0001c0001t0002g0149 a0001c0001t0002g0175 a0001c0001t0002g0182 others(51): Show |
60 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.153+2108A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981836 | |||||||
chr7:22981843 | C | T | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+2101G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981843 | |||||||
chr7:22981888 | A | C | 127 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(124): Show |
145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.153+2056T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981888 | |||||||
chr7:22981896 | A | G | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.153+2048T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981896 | |||||||
chr7:22982034 | G | A | 39 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(36): Show |
55 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.153+1910C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982034 | |||||||
chr7:22982053 | C | T | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.153+1891G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982053 | |||||||
chr7:22982110 | T | TA | 9 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0076g0054 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+1833dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982110 | |||||||
chr7:22982140 | C | G | 3 | a0001c0001t0003g0173 a0001c0001t0003g0183 a0001c0001t0006g0004 |
6 | HG01099.hp1 HG02148.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1804G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982140 | |||||||
chr7:22982178 | G | T | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+1766C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982178 | |||||||
chr7:22982291 | G | A | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.153+1653C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982291 | |||||||
chr7:22982422 | T | C | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.153+1522A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982422 | |||||||
chr7:22982565 | T | G | 1 | a0001c0002t0001g0279 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.153+1379A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982565 | |||||||
chr7:22982828 | T | C | 197 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(194): Show |
234 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.153+1116A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982828 | |||||||
chr7:22982845 | T | TC | 44 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(41): Show |
60 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.153+1098dupG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982845 | |||||||
chr7:22982895 | T | C | 2 | a0001c0002t0001g0286 a0001c0002t0041g0282 |
2 | HG01361.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.153+1049A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982895 | |||||||
chr7:22982926 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153+1018G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982926 | |||||||
chr7:22982953 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.153+991A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982953 | |||||||
chr7:22983066 | T | C | 3 | a0001c0002t0021g0230 a0001c0002t0034g0226 a0001c0002t0034g0299 |
3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.153+878A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983066 | |||||||
chr7:22983092 | G | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+852C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983092 | |||||||
chr7:22983185 | C | T | 1 | a0001c0001t0014g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153+759G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983185 | |||||||
chr7:22983198 | G | A | 51 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(48): Show |
70 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.153+746C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983198 | |||||||
chr7:22983212 | C | T | 23 | a0001c0001t0007g0219 a0001c0002t0007g0005 a0001c0002t0007g0015 others(20): Show |
29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+732G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983212 | |||||||
chr7:22983320 | C | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.153+624G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983320 | |||||||
chr7:22983328 | C | CA | 52 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(49): Show |
68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.153+615dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983328 | |||||||
chr7:22983381 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+563A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983381 | |||||||
chr7:22983415 | C | T | 1 | a0001c0002t0007g0204 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.153+529G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983415 | |||||||
chr7:22983529 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+415G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983529 | |||||||
chr7:22983547 | T | C | 1 | a0001c0001t0085g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.153+397A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983547 | |||||||
chr7:22983662 | G | A | 2 | a0001c0002t0035g0059 a0001c0002t0091g0058 |
2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+282C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983662 | |||||||
chr7:22983845 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+99G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983845 | |||||||
chr7:22984074 | C | T | 1 | a0001c0001t0006g0330 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-29G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984074 | |||||||
chr7:22984202 | G | A | 1 | a0001c0002t0098g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52-157C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984202 | |||||||
chr7:22984210 | C | A | 1 | a0001c0002t0083g0288 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.52-165G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984210 | |||||||
chr7:22984335 | A | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-290T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984335 | |||||||
chr7:22984339 | TAAAAC | T | 3 | a0001c0002t0010g0290 a0001c0002t0021g0289 a0001c0002t0022g0291 |
3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.52-299_52-295delGT others(3): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984339 | |||||||
chr7:22984648 | G | A | 1 | a0001c0001t0014g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.52-603C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984648 | |||||||
chr7:22984657 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52-612G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984657 | |||||||
chr7:22984658 | G | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-613C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984658 | |||||||
chr7:22984716 | G | C | 1 | a0001c0001t0002g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.52-671C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984716 | |||||||
chr7:22984731 | G | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-686C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984731 | |||||||
chr7:22984789 | G | A | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-744C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984789 | |||||||
chr7:22984929 | A | G | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-884T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984929 | |||||||
chr7:22984944 | TA | T | 5 | a0001c0001t0030g0077 a0001c0001t0030g0127 a0001c0001t0066g0128 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-900delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984944 | |||||||
chr7:22985107 | CCT | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1064_52-1063del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985107 | |||||||
chr7:22985111 | CAG | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1068_52-1067del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985111 | |||||||
chr7:22985117 | G | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1072C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985117 | |||||||
chr7:22985118 | T | C | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1073A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985118 | |||||||
chr7:22985176 | A | G | 50 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(47): Show |
69 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.52-1131T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985176 | |||||||
chr7:22985301 | C | A | 128 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(125): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-1256G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985301 | |||||||
chr7:22985337 | A | C | 1 | a0001c0001t0002g0149 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.52-1292T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985337 | |||||||
chr7:22985388 | A | C | 1 | a0001c0001t0013g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52-1343T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985388 | |||||||
chr7:22985389 | A | C | 3 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0001t0072g0329 |
3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.52-1344T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985389 | |||||||
chr7:22985460 | T | C | 129 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-1415A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985460 | |||||||
chr7:22985556 | C | G | 1 | a0001c0002t0005g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52-1511G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985556 | |||||||
chr7:22985600 | C | T | 1 | a0001c0002t0007g0205 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.52-1555G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985600 | |||||||
chr7:22985621 | T | C | 1 | a0001c0001t0006g0082 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.52-1576A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985621 | |||||||
chr7:22985641 | C | T | 1 | a0001c0002t0091g0058 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52-1596G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985641 | |||||||
chr7:22985669 | A | G | 2 | a0001c0002t0090g0287 a0001c0002t0094g0224 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.52-1624T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985669 | |||||||
chr7:22985688 | C | A | 2 | a0001c0002t0001g0281 a0001c0002t0001g0285 |
2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.52-1643G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985688 | |||||||
chr7:22985740 | G | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-1695C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985740 | |||||||
chr7:22985822 | T | C | 1 | a0001c0001t0014g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.52-1777A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985822 | |||||||
chr7:22985964 | T | C | 2 | a0001c0002t0001g0270 a0001c0002t0001g0280 |
2 | NA18946.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.52-1919A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985964 | |||||||
chr7:22986028 | T | TTA | 124 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0223 others(121): Show |
140 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.52-1985_52-1984dup others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986028 | |||||||
chr7:22986028 | T | TTATA | 5 | a0001c0002t0001g0008 a0001c0002t0001g0232 a0001c0002t0001g0286 others(2): Show |
7 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-1987_52-1984dup others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986028 | |||||||
chr7:22986061 | G | C | 1 | a0001c0001t0065g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.52-2016C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986061 | |||||||
chr7:22986100 | T | C | 1 | a0001c0002t0001g0267 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.52-2055A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986100 | |||||||
chr7:22986272 | C | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2227G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986272 | |||||||
chr7:22986511 | T | C | 44 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(41): Show |
60 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.52-2466A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986511 | |||||||
chr7:22986569 | T | A | 26 | a0001c0002t0010g0020 a0001c0002t0010g0227 a0001c0002t0010g0260 others(23): Show |
27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.52-2524A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986569 | |||||||
chr7:22986576 | G | A | 1 | a0001c0002t0010g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.52-2531C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986576 | |||||||
chr7:22986635 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.52-2590G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986635 | |||||||
chr7:22986706 | T | C | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-2661A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986706 | |||||||
chr7:22986817 | C | T | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2772G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986817 | |||||||
chr7:22986849 | A | G | 1 | a0004c0004t0029g0012 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52-2804T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986849 | |||||||
chr7:22986946 | G | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2901C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986946 | |||||||
chr7:22987028 | C | T | 129 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-2983G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987028 | |||||||
chr7:22987166 | T | C | 2 | a0001c0002t0001g0281 a0001c0002t0001g0285 |
2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.52-3121A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987166 | |||||||
chr7:22987219 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52-3174A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987219 | |||||||
chr7:22987228 | C | T | 1 | a0001c0002t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.52-3183G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987228 | |||||||
chr7:22987233 | A | G | 1 | a0001c0002t0010g0292 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.52-3188T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987233 | |||||||
chr7:22987274 | C | T | 1 | a0001c0002t0005g0238 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.52-3229G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987274 | |||||||
chr7:22987289 | G | A | 46 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(43): Show |
65 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.52-3244C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987289 | |||||||
chr7:22987309 | A | T | 128 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(125): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-3264T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987309 | |||||||
chr7:22987323 | G | A | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0136 |
3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.52-3278C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987323 | |||||||
chr7:22987374 | C | A | 15 | a0001c0002t0012g0189 a0001c0002t0012g0190 a0001c0002t0012g0191 others(12): Show |
15 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-3329G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987374 | |||||||
chr7:22987401 | A | G | 1 | a0001c0002t0005g0252 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.52-3356T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987401 | |||||||
chr7:22987431 | C | T | 1 | a0001c0002t0100g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.52-3386G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987431 | |||||||
chr7:22987438 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.52-3393G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987438 | |||||||
chr7:22987473 | A | G | 129 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-3428T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987473 | |||||||
chr7:22987694 | A | C | 1 | a0001c0002t0106g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.51+3367T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987694 | |||||||
chr7:22987867 | T | A | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51+3194A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987867 | |||||||
chr7:22987878 | T | C | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.51+3183A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987878 | |||||||
chr7:22987928 | T | C | 1 | a0001c0006t0006g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.51+3133A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987928 | |||||||
chr7:22988064 | G | A | 1 | a0001c0001t0066g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51+2997C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988064 | |||||||
chr7:22988076 | TTTTGCCT others(7): Show |
T | 129 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.51+2971_51+2984del others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988076 | |||||||
chr7:22988108 | CAT | C | 4 | a0001c0002t0005g0253 a0001c0002t0035g0301 a0001c0002t0090g0287 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2951_51+2952del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988108 | |||||||
chr7:22988422 | T | C | 191 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(188): Show |
228 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.51+2639A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988422 | |||||||
chr7:22988434 | T | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+2627A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988434 | |||||||
chr7:22988465 | A | G | 1 | a0001c0001t0013g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+2596T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988465 | |||||||
chr7:22988632 | C | T | 9 | a0001c0002t0010g0264 a0001c0002t0010g0290 a0001c0002t0010g0292 others(6): Show |
9 | HG01243.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+2429G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988632 | |||||||
chr7:22988686 | C | T | 158 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(155): Show |
189 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.51+2375G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988686 | |||||||
chr7:22988716 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+2345G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988716 | |||||||
chr7:22988891 | C | T | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.51+2170G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988891 | |||||||
chr7:22988991 | G | T | 37 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(34): Show |
53 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.51+2070C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988991 | |||||||
chr7:22989007 | T | C | 13 | a0001c0002t0012g0189 a0001c0002t0012g0190 a0001c0002t0012g0191 others(10): Show |
13 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2054A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989007 | |||||||
chr7:22989131 | C | T | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.51+1930G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989131 | |||||||
chr7:22989168 | A | G | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1893T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989168 | |||||||
chr7:22989230 | C | CA | 193 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(190): Show |
230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.51+1830dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989230 | |||||||
chr7:22989253 | C | T | 1 | a0001c0002t0005g0237 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.51+1808G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989253 | |||||||
chr7:22989268 | A | G | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1793T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989268 | |||||||
chr7:22989285 | A | AAC | 93 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0081 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.51+1774_51+1775dup others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | A | AACAC | 10 | a0001c0001t0002g0065 a0001c0001t0003g0086 a0001c0001t0006g0154 others(7): Show |
10 | HG01433.hp1 HG02132.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.51+1772_51+1775dup others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | A | AACACAC | 4 | a0001c0001t0003g0143 a0001c0001t0003g0173 a0001c0001t0009g0148 others(1): Show |
4 | HG00673.hp1 HG02148.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1770_51+1775dup others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | A | AACACACA others(3): Show |
2 | a0001c0001t0002g0182 a0001c0001t0009g0150 |
2 | NA18968.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.51+1766_51+1775dup others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | A | AACACACA others(5): Show |
1 | a0001c0001t0002g0149 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.51+1764_51+1775dup others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AAC | A | 5 | a0001c0001t0002g0133 a0001c0001t0055g0043 a0001c0001t0070g0042 others(2): Show |
5 | HG01978.hp2 HG02071.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+1774_51+1775del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACAC | A | 14 | a0001c0001t0013g0122 a0001c0001t0013g0135 a0001c0001t0015g0002 others(11): Show |
17 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1772_51+1775del others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACACAC | A | 13 | a0001c0001t0003g0057 a0001c0001t0024g0030 a0001c0001t0030g0077 others(10): Show |
13 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+1770_51+1775del others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACACACA others(5): Show |
A | 1 | a0001c0002t0092g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+1764_51+1775del others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACACACA others(7): Show |
A | 2 | a0001c0002t0107g0269 a0001c0002t0108g0283 |
2 | NA18991.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.51+1762_51+1775del others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACACACA others(9): Show |
A | 164 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(161): Show |
198 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.51+1760_51+1775del others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989285 | AACACACA others(11): Show |
A | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1758_51+1775del others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | |||||||
chr7:22989287 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0076 a0005c0010t0002g0187 |
3 | HG00140.hp2 HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.51+1774G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989287 | |||||||
chr7:22989402 | C | G | 1 | a0001c0002t0005g0236 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.51+1659G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989402 | |||||||
chr7:22989413 | C | T | 207 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(204): Show |
244 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.51+1648G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989413 | |||||||
chr7:22989428 | A | T | 192 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(189): Show |
229 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.51+1633T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989428 | |||||||
chr7:22989467 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1594G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989467 | |||||||
chr7:22989526 | AT | A | 192 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(189): Show |
229 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.51+1534delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989526 | |||||||
chr7:22989530 | T | A | 42 | a0001c0001t0002g0065 a0001c0001t0002g0079 a0001c0001t0002g0081 others(39): Show |
42 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.51+1531A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989530 | |||||||
chr7:22989531 | T | A | 5 | a0001c0001t0015g0039 a0001c0001t0015g0040 a0001c0001t0037g0034 others(2): Show |
5 | HG00738.hp2 HG02896.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1530A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989531 | |||||||
chr7:22989534 | T | A | 1 | a0001c0001t0065g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.51+1527A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989534 | |||||||
chr7:22989610 | T | C | 197 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(194): Show |
234 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.51+1451A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989610 | |||||||
chr7:22989775 | A | T | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.51+1286T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989775 | |||||||
chr7:22989778 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.51+1283G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989778 | |||||||
chr7:22989789 | T | C | 4 | a0001c0002t0005g0027 a0001c0002t0005g0252 a0001c0002t0005g0253 others(1): Show |
5 | HG00280.hp2 HG01175.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1272A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989789 | |||||||
chr7:22989847 | G | A | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1214C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989847 | |||||||
chr7:22989888 | A | G | 128 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(125): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.51+1173T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989888 | |||||||
chr7:22989950 | A | G | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1111T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989950 | |||||||
chr7:22990341 | A | G | 2 | a0001c0001t0019g0333 a0001c0001t0019g0334 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.51+720T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990341 | |||||||
chr7:22990356 | T | C | 1 | a0001c0001t0020g0075 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.51+705A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990356 | |||||||
chr7:22990546 | C | T | 37 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(34): Show |
53 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.51+515G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990546 | |||||||
chr7:22990610 | G | T | 1 | a0001c0002t0007g0205 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.51+451C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990610 | |||||||
chr7:22990613 | C | T | 193 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(190): Show |
230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.51+448G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990613 | |||||||
chr7:22990984 | A | T | 4 | a0001c0002t0010g0264 a0001c0002t0010g0293 a0001c0002t0010g0295 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+77T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990984 | |||||||
chr7:22991168 | G | A | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-29C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991168 | |||||||
chr7:22991396 | A | G | 1 | a0001c0002t0007g0205 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-28-257T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991396 | |||||||
chr7:22991505 | C | G | 73 | a0001c0001t0002g0149 a0001c0001t0002g0175 a0001c0001t0002g0182 others(70): Show |
79 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-28-366G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991505 | |||||||
chr7:22991645 | T | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-506A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991645 | |||||||
chr7:22991714 | G | A | 192 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(189): Show |
229 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-28-575C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991714 | |||||||
chr7:22991759 | T | C | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-620A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991759 | |||||||
chr7:22991812 | T | C | 1 | a0001c0001t0004g0326 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-28-673A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991812 | |||||||
chr7:22992043 | C | A | 2 | a0001c0001t0026g0311 a0001c0001t0026g0321 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-28-904G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992043 | |||||||
chr7:22992144 | T | TTAC | 130 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(127): Show |
148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-1006_-28-1005i others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992144 | |||||||
chr7:22992207 | G | A | 1 | a0001c0002t0005g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-28-1068C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992207 | |||||||
chr7:22992287 | T | A | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-1148A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992287 | |||||||
chr7:22992331 | C | T | 1 | a0001c0001t0016g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28-1192G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992331 | |||||||
chr7:22992378 | G | A | 38 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(35): Show |
54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28-1239C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992378 | |||||||
chr7:22992467 | A | G | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-1328T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992467 | |||||||
chr7:22992676 | T | C | 26 | a0001c0002t0010g0020 a0001c0002t0010g0227 a0001c0002t0010g0260 others(23): Show |
27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-1537A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992676 | |||||||
chr7:22992802 | G | C | 1 | a0001c0002t0090g0287 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-1663C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992802 | |||||||
chr7:22993086 | T | A | 130 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(127): Show |
148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-1947A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993086 | |||||||
chr7:22993120 | T | C | 2 | a0001c0001t0008g0309 a0001c0001t0008g0312 |
2 | HG01256.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-28-1981A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993120 | |||||||
chr7:22993151 | A | G | 3 | a0001c0002t0010g0290 a0001c0002t0021g0289 a0001c0002t0022g0291 |
3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-2012T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993151 | |||||||
chr7:22993250 | T | C | 11 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(8): Show |
17 | HG00423.hp1 HG01928.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-2111A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993250 | |||||||
chr7:22993341 | G | T | 1 | a0001c0001t0070g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-28-2202C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993341 | |||||||
chr7:22993506 | A | G | 6 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-2367T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993506 | |||||||
chr7:22993610 | G | A | 3 | a0001c0002t0010g0290 a0001c0002t0021g0289 a0001c0002t0022g0291 |
3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-2471C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993610 | |||||||
chr7:22993685 | A | AAC | 11 | a0001c0001t0003g0057 a0001c0001t0008g0312 a0001c0001t0033g0049 others(8): Show |
11 | HG01081.hp2 HG01256.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-2548_-28-2547d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993685 | |||||||
chr7:22993707 | T | C | 1 | a0001c0001t0013g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-28-2568A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993707 | |||||||
chr7:22993807 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-28-2668C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993807 | |||||||
chr7:22994046 | C | T | 197 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(194): Show |
234 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-2907G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994046 | |||||||
chr7:22994128 | G | C | 1 | a0001c0002t0007g0217 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-28-2989C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994128 | |||||||
chr7:22994208 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0107 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-28-3069C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994208 | |||||||
chr7:22994323 | G | A | 1 | a0001c0002t0090g0287 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-3184C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994323 | |||||||
chr7:22994372 | G | A | 49 | a0001c0001t0002g0149 a0001c0001t0002g0182 a0001c0001t0003g0007 others(46): Show |
55 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28-3233C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994372 | |||||||
chr7:22994496 | T | C | 105 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(102): Show |
117 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-28-3357A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994496 | |||||||
chr7:22994662 | C | T | 1 | a0001c0002t0109g0268 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-28-3523G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994662 | |||||||
chr7:22994678 | T | C | 83 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(80): Show |
108 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.-28-3539A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994678 | |||||||
chr7:22994901 | C | T | 5 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(2): Show |
8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-3762G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994901 | |||||||
chr7:22995180 | C | A | 79 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(76): Show |
90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-28-4041G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995180 | |||||||
chr7:22995255 | C | T | 6 | a0001c0001t0003g0057 a0001c0001t0076g0054 a0001c0001t0078g0056 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4116G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995255 | |||||||
chr7:22995256 | G | A | 1 | a0001c0001t0016g0147 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28-4117C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995256 | |||||||
chr7:22995344 | A | T | 8 | a0001c0001t0011g0308 a0001c0001t0015g0002 a0001c0001t0015g0039 others(5): Show |
11 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-4205T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995344 | |||||||
chr7:22995376 | A | T | 130 | a0001c0001t0007g0219 a0001c0002t0001g0001 a0001c0002t0001g0008 others(127): Show |
148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-4237T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995376 | |||||||
chr7:22995431 | T | C | 197 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(194): Show |
234 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-4292A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995431 | |||||||
chr7:22995487 | T | C | 1 | a0001c0002t0010g0292 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28-4348A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995487 | |||||||
chr7:22995513 | T | C | 1 | a0001c0002t0007g0218 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-28-4374A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995513 | |||||||
chr7:22995641 | G | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-4502C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995641 | |||||||
chr7:22995646 | T | A | 4 | a0001c0002t0001g0008 a0001c0002t0001g0232 a0001c0002t0001g0286 others(1): Show |
6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4507A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995646 | |||||||
chr7:22995650 | CAT | C | 106 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(103): Show |
118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28-4513_-28-4512d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995650 | |||||||
chr7:22995675 | A | G | 106 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(103): Show |
118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28-4536T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995675 | |||||||
chr7:22995724 | T | G | 1 | a0001c0001t0008g0327 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-28-4585A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995724 | |||||||
chr7:22995725 | G | A | 3 | a0001c0002t0021g0230 a0001c0002t0034g0226 a0001c0002t0034g0299 |
3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28-4586C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995725 | |||||||
chr7:22995781 | G | A | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28-4642C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995781 | |||||||
chr7:22995843 | T | C | 4 | a0001c0002t0010g0264 a0001c0002t0010g0293 a0001c0002t0010g0295 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-4704A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995843 | |||||||
chr7:22995898 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-28-4759C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995898 | |||||||
chr7:22995970 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-4831G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995970 | |||||||
chr7:22996033 | G | A | 107 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-4894C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996033 | |||||||
chr7:22996125 | T | G | 10 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(7): Show |
13 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28-4986A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996125 | |||||||
chr7:22996196 | G | C | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-5057C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996196 | |||||||
chr7:22996288 | G | A | 2 | a0001c0002t0090g0287 a0001c0002t0094g0224 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-28-5149C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996288 | |||||||
chr7:22996292 | CA | C | 8 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0004g0310 others(5): Show |
8 | HG01516.hp2 HG02965.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-5154delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996292 | |||||||
chr7:22996454 | G | T | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28-5315C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996454 | |||||||
chr7:22996469 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-5330A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996469 | |||||||
chr7:22996476 | T | C | 2 | a0001c0001t0006g0104 a0001c0001t0006g0105 |
2 | NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-28-5337A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996476 | |||||||
chr7:22996582 | G | A | 2 | a0001c0002t0012g0256 a0001c0002t0012g0257 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-28-5443C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996582 | |||||||
chr7:22996597 | T | TA | 12 | a0001c0001t0002g0076 a0001c0001t0002g0182 a0001c0001t0003g0173 others(9): Show |
12 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-5459dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | T | TAAAA | 8 | a0001c0002t0001g0232 a0001c0002t0001g0263 a0001c0002t0001g0266 others(5): Show |
8 | HG01070.hp2 HG01496.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-5462_-28-5459d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | T | TAAAAA | 31 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0223 others(28): Show |
39 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-28-5463_-28-5459d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | T | TAAAAAA | 31 | a0001c0002t0001g0284 a0001c0002t0001g0285 a0001c0002t0001g0286 others(28): Show |
32 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.-28-5464_-28-5459d others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | TA | T | 61 | a0001c0001t0002g0065 a0001c0001t0002g0069 a0001c0001t0002g0070 others(58): Show |
61 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-28-5459delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | TAA | T | 58 | a0001c0001t0002g0067 a0001c0001t0002g0081 a0001c0001t0002g0336 others(55): Show |
67 | HG00280.hp2 HG01074.hp2 HG01169.hp1 others(64): Show |
intron_variant | MODIFIER | c.-28-5460_-28-5459d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | TAAAAA | T | 6 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(3): Show |
9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-5463_-28-5459d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | TAAAAAAA others(1): Show |
T | 39 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(36): Show |
53 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-28-5466_-28-5459d others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996597 | TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0111g0300 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-28-5469_-28-5459d others(13): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | |||||||
chr7:22996770 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-5631G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996770 | |||||||
chr7:22996829 | C | T | 1 | a0001c0002t0038g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-28-5690G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996829 | |||||||
chr7:22996849 | T | C | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-5710A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996849 | |||||||
chr7:22997005 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-5866C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997005 | |||||||
chr7:22997072 | A | G | 38 | a0001c0001t0002g0079 a0001c0001t0003g0057 a0001c0001t0007g0219 others(35): Show |
44 | HG01081.hp2 HG01169.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-5933T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997072 | |||||||
chr7:22997152 | C | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-6013G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997152 | |||||||
chr7:22997170 | A | T | 1 | a0001c0002t0012g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-6031T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997170 | |||||||
chr7:22997173 | A | G | 26 | a0001c0002t0010g0020 a0001c0002t0010g0227 a0001c0002t0010g0260 others(23): Show |
27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-6034T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997173 | |||||||
chr7:22997281 | A | G | 1 | a0001c0001t0008g0309 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-28-6142T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997281 | |||||||
chr7:22997297 | C | T | 192 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(189): Show |
229 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-28-6158G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997297 | |||||||
chr7:22997867 | T | C | 1 | a0001c0001t0078g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-28-6728A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997867 | |||||||
chr7:22997875 | G | C | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-6736C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997875 | |||||||
chr7:22997940 | T | G | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28-6801A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997940 | |||||||
chr7:22997960 | T | C | 1 | a0001c0001t0030g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28-6821A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997960 | |||||||
chr7:22997986 | AATTAGAA others(21): Show |
A | 5 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(2): Show |
5 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-6875_-28-6848d others(30): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997986 | |||||||
chr7:22997992 | A | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(1): Show |
7 | HG00423.hp1 NA18966.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-6853T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997992 | |||||||
chr7:22998040 | T | G | 1 | a0001c0002t0022g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-28-6901A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998040 | |||||||
chr7:22998208 | C | T | 1 | a0001c0001t0011g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-28-7069G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998208 | |||||||
chr7:22998334 | T | C | 1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-7195A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998334 | |||||||
chr7:22998405 | T | C | 108 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(105): Show |
120 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-28-7266A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998405 | |||||||
chr7:22998496 | T | C | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-7357A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998496 | |||||||
chr7:22998532 | A | G | 107 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-7393T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998532 | |||||||
chr7:22998566 | A | G | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-7427T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998566 | |||||||
chr7:22998607 | T | G | 5 | a0001c0001t0030g0077 a0001c0001t0030g0127 a0001c0001t0066g0128 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-7468A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998607 | |||||||
chr7:22998690 | C | T | 1 | a0001c0002t0005g0234 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-28-7551G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998690 | |||||||
chr7:22998782 | T | C | 107 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-7643A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998782 | |||||||
chr7:22998804 | C | T | 1 | a0001c0002t0094g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-7665G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998804 | |||||||
chr7:22998900 | A | G | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-7761T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998900 | |||||||
chr7:22999006 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-28-7867A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999006 | |||||||
chr7:22999031 | T | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-7892A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999031 | |||||||
chr7:22999294 | A | C | 1 | a0001c0002t0010g0020 | 2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-28-8155T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999294 | |||||||
chr7:22999381 | C | G | 1 | a0001c0002t0010g0227 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-28-8242G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999381 | |||||||
chr7:22999447 | C | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-8308G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999447 | |||||||
chr7:22999469 | A | G | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-8330T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999469 | |||||||
chr7:22999501 | G | C | 107 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-8362C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999501 | |||||||
chr7:22999507 | T | C | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-8368A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999507 | |||||||
chr7:22999624 | A | G | 129 | a0001c0001t0002g0258 a0001c0001t0007g0219 a0001c0002t0001g0001 others(126): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.-28-8485T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999624 | |||||||
chr7:22999846 | C | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-8707G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999846 | |||||||
chr7:22999938 | A | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28-8799T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999938 | |||||||
chr7:23000001 | A | T | 1 | a0001c0001t0013g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-28-8862T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000001 | |||||||
chr7:23000098 | T | G | 2 | a0001c0001t0003g0176 a0001c0001t0009g0177 |
2 | HG00558.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-28-8959A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000098 | |||||||
chr7:23000102 | G | A | 1 | a0001c0002t0041g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-28-8963C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000102 | |||||||
chr7:23000159 | T | A | 1 | a0001c0001t0032g0304 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-28-9020A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000159 | |||||||
chr7:23000340 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-28-9201T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000340 | |||||||
chr7:23000442 | A | G | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-9303T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000442 | |||||||
chr7:23000451 | T | C | 2 | a0001c0002t0023g0016 a0001c0002t0023g0220 |
3 | NA18984.hp2 NA19058.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-28-9312A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000451 | |||||||
chr7:23000476 | A | G | 1 | a0001c0001t0037g0035 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-28-9337T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000476 | |||||||
chr7:23000553 | T | C | 2 | a0001c0002t0018g0017 a0001c0002t0018g0221 |
3 | NA18943.hp2 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-28-9414A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000553 | |||||||
chr7:23000572 | A | T | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-9433T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000572 | |||||||
chr7:23000584 | T | A | 1 | a0001c0002t0098g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-28-9445A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000584 | |||||||
chr7:23000589 | T | C | 1 | a0001c0002t0038g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-28-9450A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000589 | |||||||
chr7:23000690 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-28-9551A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000690 | |||||||
chr7:23000754 | G | T | 1 | a0005c0010t0002g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28-9615C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000754 | |||||||
chr7:23000812 | G | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-9673C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000812 | |||||||
chr7:23000849 | C | T | 80 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(77): Show |
91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-28-9710G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000849 | |||||||
chr7:23000896 | T | G | 1 | a0001c0001t0067g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-28-9757A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000896 | |||||||
chr7:23000920 | GT | G | 196 | a0001c0001t0002g0258 a0001c0001t0003g0057 a0001c0001t0004g0006 others(193): Show |
233 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-28-9782delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000920 | |||||||
chr7:23001088 | A | G | 1 | a0001c0002t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-28-9949T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001088 | |||||||
chr7:23001536 | T | G | 3 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0002t0046g0038 |
3 | HG02896.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-10397A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001536 | |||||||
chr7:23001593 | T | C | 1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-10454A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001593 | |||||||
chr7:23001801 | G | A | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-10662C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001801 | |||||||
chr7:23001895 | A | AT | 134 | a0001c0001t0002g0258 a0001c0001t0007g0219 a0001c0001t0024g0029 others(131): Show |
152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-28-10757dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001895 | |||||||
chr7:23001895 | A | T | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28-10756T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001895 | |||||||
chr7:23002136 | G | GTA | 3 | a0001c0001t0006g0179 a0001c0001t0017g0130 a0001c0001t0028g0129 |
3 | NA18939.hp1 NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-28-10999_-28-1099 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | |||||||
chr7:23002136 | G | GTATATAT others(3): Show |
1 | a0001c0001t0016g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28-11007_-28-1099 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | |||||||
chr7:23002136 | G | GTATATAT others(5): Show |
1 | a0001c0001t0082g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28-11009_-28-1099 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | |||||||
chr7:23002136 | GTATA | G | 4 | a0001c0001t0002g0074 a0001c0001t0002g0076 a0001c0001t0020g0075 others(1): Show |
4 | HG00140.hp2 HG01255.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11001_-28-1099 others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | |||||||
chr7:23002153 | T | C | 43 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(40): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-11014A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002153 | |||||||
chr7:23002153 | TATATATA others(17): Show |
T | 1 | a0001c0001t0036g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-28-11038_-28-1101 others(28): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002153 | |||||||
chr7:23002155 | T | A | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
57 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-28-11016A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002155 | |||||||
chr7:23002155 | T | C | 3 | a0001c0001t0008g0022 a0001c0001t0075g0338 a0008c0009t0073g0337 |
4 | HG02622.hp2 HG02976.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-11016A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002155 | |||||||
chr7:23002156 | A | T | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
57 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-28-11017T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002156 | |||||||
chr7:23002157 | T | A | 2 | a0001c0001t0008g0022 a0008c0009t0073g0337 |
3 | HG02976.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-28-11018A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002157 | |||||||
chr7:23002157 | T | C | 76 | a0001c0001t0007g0219 a0001c0001t0072g0329 a0001c0001t0075g0338 others(73): Show |
90 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-28-11018A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002157 | |||||||
chr7:23002158 | A | T | 2 | a0001c0001t0008g0022 a0008c0009t0073g0337 |
3 | HG02976.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-28-11019T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002158 | |||||||
chr7:23002159 | T | A | 54 | a0001c0001t0072g0329 a0001c0001t0075g0338 a0001c0002t0001g0001 others(51): Show |
62 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-28-11020A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002159 | |||||||
chr7:23002159 | T | C | 75 | a0001c0001t0002g0258 a0001c0001t0007g0219 a0001c0001t0037g0034 others(72): Show |
84 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-28-11020A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002159 | |||||||
chr7:23002160 | A | T | 53 | a0001c0001t0075g0338 a0001c0002t0001g0001 a0001c0002t0001g0008 others(50): Show |
61 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-28-11021T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002160 | |||||||
chr7:23002161 | T | A | 73 | a0001c0001t0002g0258 a0001c0001t0007g0219 a0001c0002t0001g0232 others(70): Show |
82 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-28-11022A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | |||||||
chr7:23002161 | T | C | 5 | a0001c0001t0037g0034 a0001c0001t0037g0035 a0001c0002t0005g0018 others(2): Show |
6 | HG01169.hp1 HG02071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11022A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | |||||||
chr7:23002161 | TATATATA others(9): Show |
T | 2 | a0001c0001t0013g0072 a0001c0001t0013g0134 |
2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(20): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | |||||||
chr7:23002162 | A | ATATATAC others(3): Show |
1 | a0001c0001t0015g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-28-11024_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | |||||||
chr7:23002162 | A | ATATATAT others(5): Show |
3 | a0001c0001t0015g0002 a0001c0001t0015g0040 a0001c0001t0057g0041 |
6 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11024_-28-1102 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | |||||||
chr7:23002162 | A | ATATATAT others(7): Show |
2 | a0001c0001t0055g0043 a0001c0001t0070g0042 |
2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-28-11024_-28-1102 others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | |||||||
chr7:23002162 | A | T | 73 | a0001c0001t0002g0258 a0001c0001t0007g0219 a0001c0002t0001g0232 others(70): Show |
82 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-28-11023T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | |||||||
chr7:23002163 | T | A | 3 | a0001c0001t0037g0034 a0001c0002t0005g0018 a0001c0002t0005g0231 |
4 | HG02071.hp2 HG02896.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11024A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | |||||||
chr7:23002163 | T | C | 6 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 others(3): Show |
6 | HG01081.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11024A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | |||||||
chr7:23002163 | TATATATA others(7): Show |
T | 2 | a0001c0001t0013g0135 a0001c0001t0032g0303 |
2 | HG02922.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | |||||||
chr7:23002164 | A | AAT | 3 | a0001c0002t0007g0204 a0001c0002t0012g0192 a0001c0002t0012g0193 |
3 | HG01169.hp1 HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002164 | A | ACAATTAT others(29): Show |
3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(40): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002164 | A | ATACAAT | 3 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 |
3 | HG01361.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002164 | A | ATACACAA others(1): Show |
3 | a0001c0001t0079g0055 a0003c0003t0074g0053 a0003c0003t0080g0052 |
3 | HG02145.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002164 | A | ATATATAC others(3): Show |
1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-11026_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002164 | A | T | 3 | a0001c0001t0037g0034 a0001c0002t0005g0018 a0001c0002t0005g0231 |
4 | HG02071.hp2 HG02896.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11025T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | |||||||
chr7:23002165 | TATATATA others(5): Show |
T | 3 | a0001c0001t0002g0073 a0001c0001t0009g0140 a0001c0001t0060g0141 |
3 | HG01109.hp2 NA18975.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002165 | |||||||
chr7:23002167 | TATATATA others(3): Show |
T | 37 | a0001c0001t0002g0133 a0001c0001t0002g0175 a0001c0001t0002g0182 others(34): Show |
42 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002167 | |||||||
chr7:23002169 | TATATATA others(1): Show |
T | 65 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0078 others(62): Show |
80 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002169 | |||||||
chr7:23002171 | TATATAC | T | 32 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0087 others(29): Show |
33 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002171 | |||||||
chr7:23002173 | TATAC | T | 68 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0101 others(65): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002173 | |||||||
chr7:23002175 | T | C | 1 | a0001c0001t0020g0075 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-28-11036A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002175 | |||||||
chr7:23002175 | TAC | T | 80 | a0001c0001t0002g0095 a0001c0001t0002g0107 a0001c0001t0002g0258 others(77): Show |
89 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002175 | |||||||
chr7:23002177 | C | CAAATATA others(49): Show |
1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-11039_-28-1103 others(60): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002177 | |||||||
chr7:23002177 | C | T | 40 | a0001c0001t0002g0088 a0001c0001t0003g0057 a0001c0001t0006g0179 others(37): Show |
44 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-11038G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002177 | |||||||
chr7:23002186 | T | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-11047A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002186 | |||||||
chr7:23002189 | G | A | 23 | a0001c0001t0007g0219 a0001c0002t0007g0005 a0001c0002t0007g0015 others(20): Show |
29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.-28-11050C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002189 | |||||||
chr7:23002521 | A | T | 1 | a0001c0002t0021g0230 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28-11382T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002521 | |||||||
chr7:23002692 | T | C | 76 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(73): Show |
98 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-29+11233A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002692 | |||||||
chr7:23002757 | T | C | 42 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(39): Show |
58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29+11168A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002757 | |||||||
chr7:23002925 | T | C | 3 | a0001c0001t0003g0057 a0003c0003t0074g0053 a0003c0003t0080g0052 |
3 | HG02145.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-29+11000A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002925 | |||||||
chr7:23002960 | C | T | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+10965G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002960 | |||||||
chr7:23003468 | A | C | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+10457T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003468 | |||||||
chr7:23003553 | C | T | 1 | a0001c0002t0095g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-29+10372G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003553 | |||||||
chr7:23003633 | C | T | 1 | a0001c0002t0001g0228 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-29+10292G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003633 | |||||||
chr7:23003768 | A | G | 1 | a0001c0002t0012g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-29+10157T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003768 | |||||||
chr7:23003923 | C | T | 1 | a0001c0001t0003g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-29+10002G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003923 | |||||||
chr7:23003974 | TA | T | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+9950delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003974 | |||||||
chr7:23004035 | T | C | 1 | a0001c0001t0017g0132 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-29+9890A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004035 | |||||||
chr7:23004361 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29+9564A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004361 | |||||||
chr7:23004531 | T | C | 1 | a0001c0002t0034g0299 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-29+9394A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004531 | |||||||
chr7:23004535 | T | A | 1 | a0001c0001t0076g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29+9390A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004535 | |||||||
chr7:23004537 | A | G | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+9388T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004537 | |||||||
chr7:23004809 | T | C | 1 | a0001c0001t0079g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29+9116A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004809 | |||||||
chr7:23004936 | G | C | 2 | a0001c0001t0013g0134 a0001c0001t0013g0135 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+8989C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004936 | |||||||
chr7:23004936 | G | T | 6 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+8989C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004936 | |||||||
chr7:23004951 | A | G | 185 | a0001c0001t0002g0258 a0001c0001t0003g0057 a0001c0001t0004g0006 others(182): Show |
219 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-29+8974T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004951 | |||||||
chr7:23004964 | C | T | 2 | a0001c0002t0012g0189 a0001c0002t0012g0190 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29+8961G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004964 | |||||||
chr7:23005003 | C | T | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+8922G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005003 | |||||||
chr7:23005026 | C | A | 1 | a0001c0001t0006g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-29+8899G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005026 | |||||||
chr7:23005051 | C | T | 23 | a0001c0001t0007g0219 a0001c0002t0007g0005 a0001c0002t0007g0015 others(20): Show |
29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.-29+8874G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005051 | |||||||
chr7:23005093 | C | T | 3 | a0001c0001t0033g0049 a0001c0001t0033g0050 a0001c0001t0077g0051 |
3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+8832G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005093 | |||||||
chr7:23005252 | T | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+8673A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005252 | |||||||
chr7:23005320 | G | A | 94 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(91): Show |
106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-29+8605C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005320 | |||||||
chr7:23005547 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-29+8378A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005547 | |||||||
chr7:23005636 | T | C | 1 | a0001c0001t0078g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-29+8289A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005636 | |||||||
chr7:23005746 | C | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29+8179G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005746 | |||||||
chr7:23005831 | A | C | 1 | a0001c0002t0010g0227 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-29+8094T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005831 | |||||||
chr7:23005957 | C | G | 1 | a0001c0002t0034g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-29+7968G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005957 | |||||||
chr7:23006052 | C | A | 1 | a0001c0002t0111g0300 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-29+7873G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006052 | |||||||
chr7:23006220 | A | G | 1 | a0001c0002t0091g0058 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-29+7705T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006220 | |||||||
chr7:23006328 | A | G | 198 | a0001c0001t0002g0258 a0001c0001t0003g0057 a0001c0001t0004g0006 others(195): Show |
235 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.-29+7597T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006328 | |||||||
chr7:23006352 | T | C | 5 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(2): Show |
5 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+7573A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006352 | |||||||
chr7:23006508 | C | G | 1 | a0001c0001t0002g0065 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29+7417G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006508 | |||||||
chr7:23006562 | C | T | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0136 |
3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-29+7363G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006562 | |||||||
chr7:23006687 | A | T | 7 | a0001c0001t0015g0002 a0001c0001t0015g0039 a0001c0001t0015g0040 others(4): Show |
10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+7238T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006687 | |||||||
chr7:23006756 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-29+7169C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006756 | |||||||
chr7:23006802 | C | T | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+7123G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006802 | |||||||
chr7:23006850 | G | A | 1 | a0001c0001t0003g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-29+7075C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006850 | |||||||
chr7:23007261 | C | A | 1 | a0001c0001t0003g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-29+6664G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007261 | |||||||
chr7:23007281 | C | T | 1 | a0001c0001t0019g0333 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-29+6644G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007281 | |||||||
chr7:23007442 | T | A | 60 | a0001c0001t0002g0149 a0001c0001t0002g0175 a0001c0001t0002g0182 others(57): Show |
66 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-29+6483A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007442 | |||||||
chr7:23007520 | A | C | 1 | a0001c0002t0106g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+6405T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007520 | |||||||
chr7:23007848 | A | G | 1 | a0001c0001t0009g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-29+6077T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007848 | |||||||
chr7:23007850 | C | G | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+6075G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007850 | |||||||
chr7:23008119 | C | T | 193 | a0001c0001t0002g0258 a0001c0001t0003g0057 a0001c0001t0004g0006 others(190): Show |
230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.-29+5806G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008119 | |||||||
chr7:23008151 | T | C | 107 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-29+5774A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008151 | |||||||
chr7:23008200 | A | G | 28 | a0001c0001t0007g0219 a0001c0001t0024g0029 a0001c0001t0024g0030 others(25): Show |
34 | HG01169.hp1 HG01361.hp2 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29+5725T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008200 | |||||||
chr7:23008227 | C | T | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+5698G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008227 | |||||||
chr7:23008236 | T | G | 58 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(55): Show |
76 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-29+5689A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008236 | |||||||
chr7:23008342 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-29+5583C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008342 | |||||||
chr7:23008398 | A | T | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+5527T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008398 | |||||||
chr7:23008692 | T | A | 80 | a0001c0001t0003g0057 a0001c0001t0004g0006 a0001c0001t0004g0009 others(77): Show |
105 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-29+5233A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008692 | |||||||
chr7:23008856 | T | C | 1 | a0001c0002t0106g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+5069A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008856 | |||||||
chr7:23008878 | G | T | 1 | a0001c0002t0041g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-29+5047C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008878 | |||||||
chr7:23009133 | A | T | 107 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(104): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-29+4792T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009133 | |||||||
chr7:23009281 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4644A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009281 | |||||||
chr7:23009367 | T | C | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+4558A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009367 | |||||||
chr7:23009383 | T | G | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4542A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009383 | |||||||
chr7:23009432 | C | T | 1 | a0001c0001t0081g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29+4493G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009432 | |||||||
chr7:23009443 | A | C | 2 | a0001c0001t0013g0061 a0007c0007t0013g0060 |
2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-29+4482T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009443 | |||||||
chr7:23009472 | A | G | 1 | a0001c0002t0094g0224 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29+4453T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009472 | |||||||
chr7:23009483 | C | T | 1 | a0001c0002t0001g0223 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-29+4442G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009483 | |||||||
chr7:23009509 | C | G | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+4416G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009509 | |||||||
chr7:23009599 | G | A | 1 | a0001c0002t0018g0221 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-29+4326C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009599 | |||||||
chr7:23009680 | G | A | 1 | a0001c0002t0005g0027 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-29+4245C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009680 | |||||||
chr7:23009762 | G | C | 3 | a0001c0001t0025g0186 a0001c0001t0047g0185 a0001c0001t0048g0184 |
3 | NA18939.hp2 NA19010.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-29+4163C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009762 | |||||||
chr7:23009774 | A | G | 2 | a0001c0001t0011g0011 a0001c0001t0011g0046 |
3 | HG01106.hp1 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-29+4151T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009774 | |||||||
chr7:23009966 | G | T | 1 | a0001c0002t0106g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+3959C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009966 | |||||||
chr7:23009967 | T | A | 93 | a0001c0001t0002g0258 a0001c0002t0001g0001 a0001c0002t0001g0008 others(90): Show |
105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-29+3958A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009967 | |||||||
chr7:23009984 | T | C | 1 | a0005c0010t0002g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-29+3941A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009984 | |||||||
chr7:23010074 | T | G | 1 | a0001c0001t0011g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29+3851A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010074 | |||||||
chr7:23010121 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+3804A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010121 | |||||||
chr7:23010213 | T | C | 195 | a0001c0001t0002g0202 a0001c0001t0002g0258 a0001c0001t0003g0057 others(192): Show |
232 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.-29+3712A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010213 | |||||||
chr7:23010510 | C | G | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+3415G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010510 | |||||||
chr7:23010566 | T | G | 1 | a0001c0001t0013g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-29+3359A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010566 | |||||||
chr7:23010638 | T | G | 2 | a0001c0001t0032g0303 a0001c0001t0032g0304 |
2 | NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-29+3287A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010638 | |||||||
chr7:23010669 | T | C | 33 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-29+3256A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010669 | |||||||
chr7:23010779 | T | C | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+3146A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010779 | |||||||
chr7:23010794 | A | G | 2 | a0001c0002t0035g0059 a0001c0002t0091g0058 |
2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-29+3131T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010794 | |||||||
chr7:23011086 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0050g0306 a0001c0001t0054g0307 |
5 | HG00544.hp2 NA19010.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+2839G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011086 | |||||||
chr7:23011104 | G | A | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+2821C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011104 | |||||||
chr7:23011186 | T | C | 1 | a0001c0002t0007g0305 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-29+2739A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011186 | |||||||
chr7:23011537 | G | A | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+2388C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011537 | |||||||
chr7:23011743 | G | A | 1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+2182C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011743 | |||||||
chr7:23011884 | C | A | 33 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0010 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-29+2041G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011884 | |||||||
chr7:23011910 | G | C | 1 | a0001c0001t0072g0329 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+2015C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011910 | |||||||
chr7:23011920 | T | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+2005A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011920 | |||||||
chr7:23012026 | G | C | 1 | a0001c0001t0006g0330 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29+1899C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012026 | |||||||
chr7:23012417 | C | G | 14 | a0001c0001t0003g0057 a0001c0001t0024g0029 a0001c0001t0024g0030 others(11): Show |
14 | HG01081.hp2 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29+1508G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012417 | |||||||
chr7:23012467 | G | C | 2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-29+1458C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012467 | |||||||
chr7:23012512 | G | A | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+1413C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012512 | |||||||
chr7:23012535 | T | C | 2 | a0001c0001t0019g0333 a0001c0001t0019g0334 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-29+1390A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012535 | |||||||
chr7:23012548 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-29+1377T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012548 | |||||||
chr7:23012642 | T | C | 1 | a0001c0001t0016g0335 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-29+1283A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012642 | |||||||
chr7:23012718 | C | T | 1 | a0006c0008t0008g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-29+1207G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012718 | |||||||
chr7:23012807 | A | T | 11 | a0001c0001t0011g0003 a0001c0001t0011g0011 a0001c0001t0011g0045 others(8): Show |
18 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29+1118T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012807 | |||||||
chr7:23012897 | T | C | 1 | a0001c0001t0002g0336 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29+1028A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012897 | |||||||
chr7:23012993 | A | G | 11 | a0001c0001t0011g0003 a0001c0001t0011g0011 a0001c0001t0011g0045 others(8): Show |
18 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29+932T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012993 | |||||||
chr7:23012994 | G | C | 4 | a0001c0001t0024g0029 a0001c0001t0024g0030 a0001c0001t0043g0028 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+931C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012994 | |||||||
chr7:23013114 | T | C | 1 | a0001c0002t0005g0027 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-29+811A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013114 | |||||||
chr7:23013196 | C | A | 1 | a0001c0001t0044g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+729G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013196 | |||||||
chr7:23013267 | G | A | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+658C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013267 | |||||||
chr7:23013412 | T | C | 1 | a0008c0009t0073g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+513A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013412 | |||||||
chr7:23013472 | G | A | 1 | a0001c0001t0075g0338 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+453C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013472 | |||||||
chr7:23013635 | G | T | 1 | a0001c0002t0046g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+290C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013635 | |||||||
chr7:23013645 | G | T | 2 | a0001c0002t0104g0037 a0001c0002t0105g0036 |
2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-29+280C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013645 | |||||||
chr7:23013756 | C | T | 2 | a0001c0001t0037g0034 a0001c0001t0037g0035 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+169G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013756 | |||||||
chr7:23013823 | C | T | 1 | a0001c0002t0005g0033 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29+102G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013823 |