Item | Value |
---|---|
geneid | 140545 |
ensemblid | ENSG00000105982.17 |
hgncid | 17118 |
symbol | RNF32 |
name | ring finger protein 32 |
refseq_nuc | NM_030936.4 |
refseq_prot | NP_112198.1 |
ensembl_nuc | ENST00000317955.10 |
ensembl_prot | ENSP00000315950.5 |
mane_status | MANE Select |
chr | chr7 |
start | 156640774 |
end | 156677130 |
strand | + |
ver | v1.2 |
region | chr7:156640774-156677130 |
region5000 | chr7:156635774-156682130 |
regionname0 | RNF32_chr7_156640774_156677130 |
regionname5000 | RNF32_chr7_156635774_156682130 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 362 | 200 | 26 | 41 | 90 | 8 | 33 | 70 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0002 | 0/0 | 362 | 178 | 43 | 26 | 93 | 7 | 9 | 77 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0003 | 0/0 | 362 | 50 | 14 | 2 | 30 | 1 | 3 | 24 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0004 | 0/0 | 362 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0005 | 0/0 | 362 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0006 | 0/0 | 362 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0007 | 0/0 | 362 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0008 | 0/0 | 362 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0009 | 0/0 | 362 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0010 | 0/0 | 362 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
a0011 | 0/0 | 362 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | MLKNK others(357): Show |
chr7 | 156635774 | 156682130 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1086 | 185 | 12 | 41 | 89 | 8 | 33 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0001c0004 | 0/0 | 1086 | 15 | 14 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0002c0002 | 0/0 | 1086 | 178 | 43 | 26 | 93 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0003c0003 | 0/0 | 1086 | 50 | 14 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0004c0005 | 0/0 | 1086 | 7 | 7 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0004c0012 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0005c0006 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0006c0008 | 0/0 | 1086 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0007c0007 | 0/0 | 1086 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0008c0009 | 0/0 | 1086 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0009c0013 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0010c0011 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 | ||
a0011c0010 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | ATGTT others(1081): Show |
chr7 | 156635774 | 156682130 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/1 | 1679 | 136 | 6 | 35 | 55 | 8 | 30 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0001c0001t0003 | 0/0 | 1679 | 49 | 6 | 6 | 34 | 0 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0001c0004t0002 | 0/0 | 1679 | 3 | 2 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0001c0004t0003 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0001c0004t0005 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0001c0004t0006 | 0/0 | 1679 | 10 | 10 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0002c0002t0001 | 0/0 | 1679 | 160 | 42 | 25 | 77 | 7 | 9 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0002c0002t0005 | 0/0 | 1679 | 18 | 1 | 1 | 16 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0003c0003t0002 | 0/0 | 1679 | 6 | 6 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0003c0003t0004 | 0/0 | 1679 | 42 | 6 | 2 | 30 | 1 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0003c0003t0007 | 0/0 | 1679 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGAAG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0004c0005t0002 | 0/0 | 1679 | 7 | 7 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0004c0012t0002 | 0/0 | 1679 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0005c0006t0004 | 0/0 | 1679 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0006c0008t0002 | 0/0 | 1679 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0007c0007t0001 | 0/0 | 1679 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0008c0009t0001 | 0/0 | 1679 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0009c0013t0001 | 0/0 | 1679 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0010c0011t0002 | 0/0 | 1679 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
a0011c0010t0001 | 0/0 | 1679 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | AGACG others(1674): Show |
chr7 | 156635774 | 156682130 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 27 | 1 | 4 | 16 | 1 | 5 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0005 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0014 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0003 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0001c0004t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0002 | 0/0 | 14 | 2 | 2 | 9 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0004 | 0/0 | 11 | 1 | 3 | 2 | 2 | 3 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0011 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0002c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0003c0003t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0005t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0004c0012t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0005c0006t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0006c0008t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0007c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0008c0009t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0009c0013t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0010c0011t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
a0011c0010t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0164 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0217 | EUR | GBR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0165 | EUR | FIN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | FIN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00438 | hp2 | a0003 | c0003 | t0004 | g0066 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00609 | hp2 | a0003 | c0003 | t0004 | g0083 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00639 | hp1 | a0002 | c0002 | t0005 | g0064 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01168 | hp2 | a0003 | c0003 | t0004 | g0188 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01256 | hp1 | a0003 | c0003 | t0004 | g0144 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01433 | hp1 | a0009 | c0013 | t0001 | g0011 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0139 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | IBS | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01884 | hp1 | a0004 | c0005 | t0002 | g0059 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01884 | hp2 | a0004 | c0005 | t0002 | g0267 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02015 | hp1 | a0002 | c0002 | t0005 | g0006 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02027 | hp2 | a0003 | c0003 | t0004 | g0088 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02071 | hp2 | a0002 | c0002 | t0005 | g0006 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02074 | hp2 | a0001 | c0004 | t0002 | g0222 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02132 | hp1 | a0002 | c0002 | t0005 | g0006 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02135 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02145 | hp2 | a0003 | c0003 | t0004 | g0074 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02155 | hp1 | a0003 | c0003 | t0004 | g0090 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02155 | hp2 | a0002 | c0002 | t0005 | g0006 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | CDX | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02257 | hp1 | a0002 | c0002 | t0005 | g0249 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02257 | hp2 | a0003 | c0003 | t0002 | g0189 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0079 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02280 | hp1 | a0001 | c0004 | t0006 | g0094 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02280 | hp2 | a0004 | c0005 | t0002 | g0266 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02523 | hp1 | a0003 | c0003 | t0004 | g0070 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02615 | hp1 | a0003 | c0003 | t0002 | g0228 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02622 | hp2 | a0001 | c0004 | t0002 | g0216 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02630 | hp1 | a0003 | c0003 | t0004 | g0098 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02683 | hp1 | a0006 | c0008 | t0002 | g0033 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02698 | hp1 | a0006 | c0008 | t0002 | g0033 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0231 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02723 | hp1 | a0004 | c0005 | t0002 | g0269 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02809 | hp2 | a0004 | c0012 | t0002 | g0264 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0232 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02896 | hp1 | a0001 | c0004 | t0006 | g0093 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02896 | hp2 | a0001 | c0004 | t0002 | g0163 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02897 | hp1 | a0001 | c0004 | t0006 | g0096 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0052 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02976 | hp2 | a0004 | c0005 | t0002 | g0268 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03041 | hp2 | a0001 | c0004 | t0006 | g0013 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03098 | hp1 | a0004 | c0005 | t0002 | g0265 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03098 | hp2 | a0001 | c0004 | t0006 | g0095 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03139 | hp2 | a0005 | c0006 | t0004 | g0021 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03195 | hp1 | a0001 | c0004 | t0003 | g0247 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03195 | hp2 | a0005 | c0006 | t0004 | g0021 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03209 | hp1 | a0001 | c0004 | t0006 | g0013 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03453 | hp2 | a0001 | c0004 | t0006 | g0013 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03490 | hp2 | a0003 | c0003 | t0004 | g0049 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03492 | hp1 | a0003 | c0003 | t0004 | g0049 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0078 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0097 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0256 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03927 | hp2 | a0010 | c0011 | t0002 | g0042 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04204 | hp2 | a0003 | c0003 | t0004 | g0229 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | STU | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18522 | hp1 | a0004 | c0005 | t0002 | g0059 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18747 | hp1 | a0002 | c0002 | t0005 | g0006 | EAS | CHB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18944 | hp1 | a0002 | c0002 | t0005 | g0254 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18946 | hp2 | a0002 | c0002 | t0005 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18952 | hp2 | a0003 | c0003 | t0004 | g0085 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18953 | hp1 | a0003 | c0003 | t0004 | g0068 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18954 | hp1 | a0007 | c0007 | t0001 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18956 | hp2 | a0003 | c0003 | t0004 | g0016 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18962 | hp1 | a0003 | c0003 | t0004 | g0034 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18963 | hp1 | a0003 | c0003 | t0004 | g0069 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18964 | hp1 | a0002 | c0002 | t0005 | g0244 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18968 | hp1 | a0002 | c0002 | t0005 | g0241 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18974 | hp2 | a0002 | c0002 | t0005 | g0239 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18975 | hp2 | a0003 | c0003 | t0004 | g0016 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18981 | hp1 | a0003 | c0003 | t0004 | g0072 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18982 | hp1 | a0002 | c0002 | t0005 | g0006 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18985 | hp2 | a0008 | c0009 | t0001 | g0015 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18986 | hp1 | a0003 | c0003 | t0004 | g0034 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18991 | hp1 | a0002 | c0002 | t0005 | g0055 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18991 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18992 | hp1 | a0003 | c0003 | t0004 | g0067 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18997 | hp1 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18998 | hp2 | a0003 | c0003 | t0004 | g0082 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19000 | hp2 | a0003 | c0003 | t0004 | g0084 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19003 | hp2 | a0003 | c0003 | t0004 | g0099 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19007 | hp1 | a0002 | c0002 | t0005 | g0055 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19010 | hp2 | a0003 | c0003 | t0004 | g0089 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19012 | hp2 | a0003 | c0003 | t0004 | g0080 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19030 | hp2 | a0001 | c0004 | t0005 | g0246 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19043 | hp2 | a0003 | c0003 | t0007 | g0271 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19054 | hp1 | a0003 | c0003 | t0004 | g0086 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19054 | hp2 | a0008 | c0009 | t0001 | g0015 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19055 | hp2 | a0002 | c0002 | t0005 | g0240 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19062 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19065 | hp1 | a0003 | c0003 | t0004 | g0087 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19066 | hp2 | a0003 | c0003 | t0004 | g0016 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19067 | hp1 | a0002 | c0002 | t0005 | g0242 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19068 | hp2 | a0007 | c0007 | t0001 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19072 | hp1 | a0002 | c0002 | t0005 | g0237 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19074 | hp2 | a0003 | c0003 | t0004 | g0071 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19082 | hp2 | a0011 | c0010 | t0001 | g0221 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19085 | hp1 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19087 | hp2 | a0003 | c0003 | t0004 | g0091 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19089 | hp1 | a0003 | c0003 | t0004 | g0081 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20129 | hp1 | a0003 | c0003 | t0004 | g0075 | AFR | ASW | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ASW | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20752 | hp2 | a0003 | c0003 | t0004 | g0203 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0133 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02559 | hp1 | a0001 | c0004 | t0006 | g0013 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG02559 | hp2 | a0005 | c0006 | t0004 | g0021 | AFR | ACB | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03471 | hp1 | a0001 | c0004 | t0006 | g0092 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
HG06807 | hp2 | a0003 | c0003 | t0007 | g0270 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0052 | AFR | USA | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
NA21309 | hp2 | a0001 | c0004 | t0006 | g0130 | AFR | LWK | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0148 | REF | REF | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0014 | REF | REF | RNF32_chr7_156635774_156682130 | RNF32 | chr7 | 156635774 | 156682130 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156644527 | C | A | 1 | a0011 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.44C>A | p.Ala15Glu | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 159/1679 | 44/1089 | 15/362 | chr7 | 156644527 | |||
chr7:156644606 | G | C | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.123G>C | p.Lys41Asn | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 238/1679 | 123/1089 | 41/362 | chr7 | 156644606 | |||
chr7:156644608 | C | A | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.125C>A | p.Thr42Lys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 240/1679 | 125/1089 | 42/362 | chr7 | 156644608 | |||
chr7:156644611 | A | T | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.128A>T | p.Gln43Leu | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 243/1679 | 128/1089 | 43/362 | chr7 | 156644611 | |||
chr7:156654631 | G | C | 1 | a0007 | 2 | NA18954.hp1 NA19068.hp2 |
missense_variant | MODERATE | c.330G>C | p.Trp110Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/9 | 445/1679 | 330/1089 | 110/362 | chr7 | 156654631 | |||
chr7:156675781 | T | C | 1 | a0005 | 3 | HG02559.hp2 HG03139.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.770T>C | p.Ile257Thr | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/9 | 885/1679 | 770/1089 | 257/362 | chr7 | 156675781 | |||
chr7:156675787 | G | A | 1 | a0004 | 8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
missense_variant | MODERATE | c.776G>A | p.Arg259Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/9 | 891/1679 | 776/1089 | 259/362 | chr7 | 156675787 | |||
chr7:156676429 | G | A | 2 | a0003 a0005 |
53 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(50): Show |
missense_variant | MODERATE | c.863G>A | p.Arg288Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 978/1679 | 863/1089 | 288/362 | chr7 | 156676429 | |||
chr7:156676439 | C | G | 5 | a0002 a0007 a0008 others(2): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
missense_variant | MODERATE | c.873C>G | p.His291Gln | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 988/1679 | 873/1089 | 291/362 | chr7 | 156676439 | |||
chr7:156676485 | C | T | 4 | a0002 a0007 a0009 others(1): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
missense_variant | MODERATE | c.919C>T | p.Arg307Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1034/1679 | 919/1089 | 307/362 | chr7 | 156676485 | |||
chr7:156676528 | C | T | 1 | a0006 | 2 | HG02683.hp1 HG02698.hp1 |
missense_variant | MODERATE | c.962C>T | p.Ser321Phe | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1077/1679 | 962/1089 | 321/362 | chr7 | 156676528 | |||
chr7:156676620 | C | T | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1054C>T | p.Arg352Cys | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1169/1679 | 1054/1089 | 352/362 | chr7 | 156676620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156644609 | A | T | 1 | a0010c0011 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.126A>T | p.Thr42Thr | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/9 | 241/1679 | 126/1089 | 42/362 | chr7 | 156644609 | |||
chr7:156676496 | A | G | 10 | a0001c0004 a0002c0002 a0003c0003 others(7): Show |
260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
synonymous_variant | LOW | c.930A>G | p.Ala310Ala | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1045/1679 | 930/1089 | 310/362 | chr7 | 156676496 | |||
chr7:156676589 | C | T | 1 | a0004c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1023C>T | p.Asp341Asp | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 1138/1679 | 1023/1089 | 341/362 | chr7 | 156676589 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156640777 | C | A | 1 | a0003c0003t0007 | 2 | HG06807.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-112C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3101 | chr7 | 156640777 | ||||||
chr7:156640803 | G | A | 4 | a0001c0001t0003 a0001c0004t0003 a0001c0004t0005 others(1): Show |
69 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3075 | chr7 | 156640803 | ||||||
chr7:156640804 | G | T | 1 | a0003c0003t0007 | 2 | HG06807.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-85G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/9 | 3074 | chr7 | 156640804 | ||||||
chr7:156676707 | T | C | 1 | a0001c0004t0006 | 10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 52 | chr7 | 156676707 | ||||||
chr7:156676760 | C | T | 2 | a0003c0003t0004 a0005c0006t0004 |
45 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 105 | chr7 | 156676760 | ||||||
chr7:156676926 | T | C | 7 | a0001c0004t0005 a0002c0002t0001 a0002c0002t0005 others(4): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 9/9 | 271 | chr7 | 156676926 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:156640814 | A | C | 4 | a0001c0001t0002g0061 a0001c0001t0002g0272 a0002c0002t0001g0273 others(1): Show |
5 | HG00423.hp1 HG01123.hp1 HG01257.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.-78+3A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640814 | |||||||
chr7:156640861 | C | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG02145.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-78+50C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640861 | |||||||
chr7:156640914 | T | C | 1 | a0002c0002t0005g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-78+103T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640914 | |||||||
chr7:156640985 | T | C | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG02145.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-78+174T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156640985 | |||||||
chr7:156641027 | A | C | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+216A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641027 | |||||||
chr7:156641034 | G | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-78+223G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641034 | |||||||
chr7:156641147 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-78+336T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641147 | |||||||
chr7:156641353 | T | G | 1 | a0003c0003t0004g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-78+542T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641353 | |||||||
chr7:156641452 | C | G | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+641C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641452 | |||||||
chr7:156641462 | C | T | 1 | a0001c0001t0002g0060 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-78+651C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641462 | |||||||
chr7:156641475 | T | G | 39 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0004t0006g0013 others(36): Show |
51 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-78+664T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641475 | |||||||
chr7:156641490 | G | T | 1 | a0003c0003t0004g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-78+679G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641490 | |||||||
chr7:156641491 | G | A | 37 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0004t0006g0013 others(34): Show |
49 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-78+680G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641491 | |||||||
chr7:156641523 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+712A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641523 | |||||||
chr7:156641852 | A | G | 196 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(193): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-78+1041A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641852 | |||||||
chr7:156641858 | GAACTTAT others(6): Show |
G | 7 | a0001c0001t0002g0017 a0001c0004t0006g0013 a0001c0004t0006g0092 others(4): Show |
12 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78+1048_-78+1060d others(15): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641858 | |||||||
chr7:156641981 | A | G | 42 | a0001c0001t0002g0262 a0001c0001t0003g0003 a0001c0001t0003g0031 others(39): Show |
70 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-78+1170A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156641981 | |||||||
chr7:156642029 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-78+1218G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642029 | |||||||
chr7:156642084 | A | T | 42 | a0001c0001t0002g0262 a0001c0001t0003g0003 a0001c0001t0003g0031 others(39): Show |
70 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-78+1273A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642084 | |||||||
chr7:156642181 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+1370G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642181 | |||||||
chr7:156642222 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+1411A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642222 | |||||||
chr7:156642308 | A | G | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-1493A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642308 | |||||||
chr7:156642421 | A | G | 1 | a0003c0003t0004g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-77-1380A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642421 | |||||||
chr7:156642515 | C | A | 1 | a0002c0002t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-77-1286C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642515 | |||||||
chr7:156642525 | C | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-1276C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642525 | |||||||
chr7:156642673 | G | A | 1 | a0001c0001t0003g0233 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-77-1128G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642673 | |||||||
chr7:156642703 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-1098A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642703 | |||||||
chr7:156642746 | T | G | 1 | a0002c0002t0001g0162 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-77-1055T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642746 | |||||||
chr7:156642750 | C | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-1051C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642750 | |||||||
chr7:156642756 | G | A | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-77-1045G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642756 | |||||||
chr7:156642850 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-77-951C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642850 | |||||||
chr7:156642905 | G | A | 10 | a0001c0001t0002g0073 a0003c0003t0004g0009 a0003c0003t0004g0016 others(7): Show |
17 | HG00558.hp2 HG02135.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.-77-896G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156642905 | |||||||
chr7:156643086 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-715G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643086 | |||||||
chr7:156643103 | A | G | 1 | a0002c0002t0001g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77-698A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643103 | |||||||
chr7:156643344 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-457A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643344 | |||||||
chr7:156643426 | C | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-375C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 1/8 | chr7 | 156643426 | |||||||
chr7:156643968 | A | G | 1 | a0002c0002t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.15+76A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156643968 | |||||||
chr7:156644021 | G | A | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.15+129G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644021 | |||||||
chr7:156644042 | C | CA | 3 | a0003c0003t0004g0074 a0003c0003t0004g0097 a0003c0003t0004g0098 |
3 | HG02145.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.15+151dupA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 156644042 | ||||||
chr7:156644075 | C | T | 220 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(217): Show |
348 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.15+183C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644075 | |||||||
chr7:156644127 | G | T | 2 | a0002c0002t0001g0051 a0002c0002t0001g0226 |
3 | NA18955.hp1 NA19007.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.15+235G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644127 | |||||||
chr7:156644154 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15+262C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644154 | |||||||
chr7:156644171 | G | A | 193 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(190): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.15+279G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644171 | |||||||
chr7:156644252 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-247G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644252 | |||||||
chr7:156644300 | A | C | 102 | a0001c0001t0002g0142 a0001c0001t0002g0186 a0001c0001t0002g0199 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.16-199A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644300 | |||||||
chr7:156644356 | C | T | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.16-143C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 2/8 | chr7 | 156644356 | |||||||
chr7:156644777 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.274+20C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156644777 | |||||||
chr7:156644952 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+195A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156644952 | |||||||
chr7:156645030 | T | G | 2 | a0002c0002t0001g0076 a0003c0003t0004g0075 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274+273T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645030 | |||||||
chr7:156645146 | T | C | 40 | a0001c0001t0002g0073 a0001c0004t0006g0013 a0001c0004t0006g0092 others(37): Show |
50 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.274+389T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645146 | |||||||
chr7:156645378 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274+621A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645378 | |||||||
chr7:156645394 | A | G | 2 | a0002c0002t0001g0223 a0002c0002t0001g0224 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.274+637A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645394 | |||||||
chr7:156645524 | T | G | 1 | a0004c0012t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274+767T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645524 | |||||||
chr7:156645559 | A | G | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.274+802A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645559 | |||||||
chr7:156645729 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+972T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645729 | |||||||
chr7:156645768 | T | C | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+1011T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645768 | |||||||
chr7:156645821 | G | A | 101 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0216 others(98): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.274+1064G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645821 | |||||||
chr7:156645851 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+1094A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645851 | |||||||
chr7:156645969 | C | T | 6 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(3): Show |
9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+1212C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156645969 | |||||||
chr7:156646030 | G | A | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.274+1273G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646030 | |||||||
chr7:156646040 | T | C | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.274+1283T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646040 | |||||||
chr7:156646075 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+1318G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646075 | |||||||
chr7:156646103 | T | C | 95 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0216 others(92): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.274+1346T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646103 | |||||||
chr7:156646252 | A | C | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+1495A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646252 | |||||||
chr7:156646321 | T | C | 1 | a0002c0002t0001g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.274+1564T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646321 | |||||||
chr7:156646352 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0060 a0001c0001t0002g0140 |
6 | HG01167.hp2 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1595C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646352 | |||||||
chr7:156646392 | C | T | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+1635C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646392 | |||||||
chr7:156646450 | T | A | 2 | a0002c0002t0001g0076 a0003c0003t0004g0075 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274+1693T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646450 | |||||||
chr7:156646861 | G | GT | 9 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0101 others(6): Show |
19 | HG00423.hp1 NA18747.hp2 NA18951.hp1 others(16): Show |
intron_variant | MODIFIER | c.274+2112dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156646861 | ||||||
chr7:156646914 | C | T | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274+2157C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156646914 | |||||||
chr7:156647043 | G | A | 4 | a0002c0002t0001g0065 a0002c0002t0001g0164 a0002c0002t0001g0165 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+2286G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647043 | |||||||
chr7:156647098 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.274+2341C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647098 | |||||||
chr7:156647132 | G | A | 43 | a0001c0001t0002g0017 a0001c0001t0003g0003 a0001c0001t0003g0031 others(40): Show |
73 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.274+2375G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647132 | |||||||
chr7:156647153 | G | GT | 36 | a0001c0001t0002g0073 a0001c0001t0003g0058 a0001c0001t0003g0260 others(33): Show |
44 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.274+2405dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647153 | ||||||
chr7:156647163 | A | T | 199 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(196): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.274+2406A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647163 | |||||||
chr7:156647167 | T | TTTTG | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2418_274+2421d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647167 | ||||||
chr7:156647195 | CT | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2444delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156647195 | ||||||
chr7:156647208 | T | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0216 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+2451T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647208 | |||||||
chr7:156647374 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+2617A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647374 | |||||||
chr7:156647541 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274+2784C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647541 | |||||||
chr7:156647654 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.274+2897C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647654 | |||||||
chr7:156647862 | A | T | 1 | a0004c0012t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274+3105A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647862 | |||||||
chr7:156647996 | G | C | 1 | a0001c0001t0002g0101 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.274+3239G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156647996 | |||||||
chr7:156648028 | T | A | 1 | a0003c0003t0004g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.274+3271T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648028 | |||||||
chr7:156648028 | TG | T | 29 | a0001c0001t0002g0073 a0003c0003t0004g0009 a0003c0003t0004g0016 others(26): Show |
37 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.274+3272delG | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648028 | |||||||
chr7:156648029 | G | GT | 111 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(108): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+3284dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156648029 | ||||||
chr7:156648029 | G | T | 9 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0003c0003t0004g0074 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+3272G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648029 | |||||||
chr7:156648066 | G | A | 1 | a0001c0001t0003g0031 | 3 | HG02083.hp1 HG02129.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.274+3309G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648066 | |||||||
chr7:156648167 | T | C | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0216 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.274+3410T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648167 | |||||||
chr7:156648209 | G | A | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+3452G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648209 | |||||||
chr7:156648411 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.274+3654G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648411 | |||||||
chr7:156648536 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+3779G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648536 | |||||||
chr7:156648615 | T | A | 1 | a0002c0002t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.274+3858T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648615 | |||||||
chr7:156648625 | G | A | 1 | a0001c0001t0003g0053 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.274+3868G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156648625 | |||||||
chr7:156649156 | C | CT | 8 | a0002c0002t0001g0218 a0004c0005t0002g0059 a0004c0005t0002g0265 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+4410dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156649156 | ||||||
chr7:156649234 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274+4477C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649234 | |||||||
chr7:156649295 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+4538C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649295 | |||||||
chr7:156649341 | T | C | 95 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0002c0002t0001g0002 others(92): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.274+4584T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649341 | |||||||
chr7:156649481 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.274+4724G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649481 | |||||||
chr7:156649498 | G | A | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+4741G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649498 | |||||||
chr7:156649509 | T | C | 200 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(197): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.274+4752T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649509 | |||||||
chr7:156649701 | T | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4875T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649701 | |||||||
chr7:156649711 | G | A | 6 | a0001c0004t0002g0222 a0002c0002t0001g0015 a0002c0002t0001g0030 others(3): Show |
10 | HG00423.hp2 HG01069.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-4865G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649711 | |||||||
chr7:156649747 | G | A | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-4829G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649747 | |||||||
chr7:156649747 | G | T | 1 | a0003c0003t0004g0091 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.275-4829G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156649747 | |||||||
chr7:156650025 | G | GCT | 200 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(197): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.275-4550_275-4549d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156650025 | ||||||
chr7:156650204 | G | A | 1 | a0003c0003t0004g0067 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.275-4372G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650204 | |||||||
chr7:156650322 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4254C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650322 | |||||||
chr7:156650350 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4226T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650350 | |||||||
chr7:156650445 | C | T | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-4131C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650445 | |||||||
chr7:156650447 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4129C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650447 | |||||||
chr7:156650475 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-4101T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650475 | |||||||
chr7:156650545 | G | T | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.275-4031G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650545 | |||||||
chr7:156650667 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3909T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650667 | |||||||
chr7:156650678 | G | A | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.275-3898G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650678 | |||||||
chr7:156650768 | C | T | 4 | a0001c0001t0003g0032 a0001c0001t0003g0256 a0001c0001t0003g0257 others(1): Show |
6 | HG00597.hp2 HG00609.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-3808C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650768 | |||||||
chr7:156650790 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3786G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156650790 | |||||||
chr7:156651000 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3576C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651000 | |||||||
chr7:156651092 | A | C | 1 | a0001c0001t0003g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.275-3484A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651092 | |||||||
chr7:156651213 | T | G | 1 | a0002c0002t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.275-3363T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651213 | |||||||
chr7:156651215 | C | CT | 9 | a0001c0001t0002g0039 a0001c0001t0002g0100 a0001c0004t0002g0163 others(6): Show |
14 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.275-3345dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | ||||||
chr7:156651215 | C | CTT | 44 | a0001c0001t0002g0017 a0001c0001t0002g0262 a0001c0001t0003g0003 others(41): Show |
74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.275-3346_275-3345d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | ||||||
chr7:156651215 | CT | C | 51 | a0001c0001t0002g0073 a0001c0001t0002g0103 a0001c0001t0002g0104 others(48): Show |
63 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.275-3345delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156651215 | ||||||
chr7:156651288 | A | G | 40 | a0001c0001t0002g0073 a0001c0004t0006g0013 a0001c0004t0006g0092 others(37): Show |
50 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.275-3288A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651288 | |||||||
chr7:156651296 | C | T | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-3280C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651296 | |||||||
chr7:156651474 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3102A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651474 | |||||||
chr7:156651511 | G | A | 6 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(3): Show |
9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-3065G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651511 | |||||||
chr7:156651522 | A | C | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-3054A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651522 | |||||||
chr7:156651545 | C | T | 29 | a0001c0001t0002g0073 a0002c0002t0001g0076 a0003c0003t0004g0009 others(26): Show |
36 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.275-3031C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651545 | |||||||
chr7:156651651 | T | C | 44 | a0001c0001t0002g0017 a0001c0001t0002g0262 a0001c0001t0003g0003 others(41): Show |
74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.275-2925T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651651 | |||||||
chr7:156651671 | C | T | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.275-2905C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651671 | |||||||
chr7:156651753 | C | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-2823C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156651753 | |||||||
chr7:156652005 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.275-2571C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652005 | |||||||
chr7:156652120 | C | T | 3 | a0002c0002t0001g0050 a0002c0002t0001g0214 a0002c0002t0001g0215 |
4 | HG03041.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-2456C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652120 | |||||||
chr7:156652285 | C | T | 1 | a0003c0003t0004g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.275-2291C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652285 | |||||||
chr7:156652303 | G | A | 4 | a0003c0003t0004g0144 a0003c0003t0007g0270 a0003c0003t0007g0271 others(1): Show |
6 | HG01256.hp1 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-2273G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652303 | |||||||
chr7:156652474 | CTTGA | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-2099_275-2096d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652474 | ||||||
chr7:156652530 | C | T | 1 | a0002c0002t0005g0254 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.275-2046C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652530 | |||||||
chr7:156652694 | A | T | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.275-1882A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652694 | |||||||
chr7:156652739 | T | TATA | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1836_275-1835i others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652739 | ||||||
chr7:156652793 | T | A | 2 | a0001c0001t0002g0018 a0001c0001t0002g0101 |
4 | NA18967.hp2 NA18975.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-1783T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652793 | |||||||
chr7:156652870 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1706A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652870 | |||||||
chr7:156652870 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.275-1706A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652870 | |||||||
chr7:156652929 | TA | T | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-1641delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156652929 | ||||||
chr7:156652948 | G | T | 1 | a0003c0003t0004g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-1628G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156652948 | |||||||
chr7:156653001 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1575A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653001 | |||||||
chr7:156653039 | T | C | 1 | a0001c0001t0003g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.275-1537T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653039 | |||||||
chr7:156653091 | GCACT | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-1476_275-1473d others(6): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156653091 | ||||||
chr7:156653200 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1376A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653200 | |||||||
chr7:156653211 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1365A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653211 | |||||||
chr7:156653220 | A | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-1356A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653220 | |||||||
chr7:156653351 | A | G | 155 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(152): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.275-1225A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653351 | |||||||
chr7:156653380 | C | T | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-1196C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653380 | |||||||
chr7:156653415 | C | T | 8 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(5): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-1161C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653415 | |||||||
chr7:156653444 | T | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.275-1132T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653444 | |||||||
chr7:156653476 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG01243.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.275-1100G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653476 | |||||||
chr7:156653556 | C | T | 2 | a0001c0004t0006g0013 a0001c0004t0006g0095 |
5 | HG02559.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-1020C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653556 | |||||||
chr7:156653618 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.275-958T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653618 | |||||||
chr7:156653624 | C | T | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-952C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653624 | |||||||
chr7:156653706 | A | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-870A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653706 | |||||||
chr7:156653802 | T | A | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-774T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653802 | |||||||
chr7:156653815 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-761A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653815 | |||||||
chr7:156653911 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.275-665G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156653911 | |||||||
chr7:156654113 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.275-463A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654113 | |||||||
chr7:156654122 | C | T | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.275-454C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654122 | |||||||
chr7:156654142 | A | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-434A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654142 | |||||||
chr7:156654154 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-422C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654154 | |||||||
chr7:156654166 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.275-410A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654166 | |||||||
chr7:156654211 | T | TA | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-359dupA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156654211 | ||||||
chr7:156654229 | CAATAT | C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0006c0008t0002g0033 |
4 | HG00738.hp2 HG01175.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-342_275-338del others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 156654229 | ||||||
chr7:156654377 | A | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.275-199A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654377 | |||||||
chr7:156654483 | A | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0146 a0001c0001t0002g0147 others(1): Show |
6 | NA18950.hp2 NA18952.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-93A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 3/8 | chr7 | 156654483 | |||||||
chr7:156654731 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.417+13C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156654731 | |||||||
chr7:156654858 | T | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.417+140T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156654858 | |||||||
chr7:156655014 | G | A | 36 | a0001c0001t0002g0186 a0002c0002t0001g0004 a0002c0002t0001g0024 others(33): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.417+296G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655014 | |||||||
chr7:156655232 | C | CGG | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+515_417+516ins others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655232 | ||||||
chr7:156655237 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.417+519G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655237 | |||||||
chr7:156655239 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+521G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655239 | |||||||
chr7:156655239 | G | GCA | 19 | a0001c0001t0002g0005 a0001c0001t0002g0022 a0001c0001t0002g0023 others(16): Show |
33 | HG00280.hp2 HG00642.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.417+544_417+545dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | ||||||
chr7:156655239 | G | GCACA | 2 | a0001c0001t0002g0040 a0001c0001t0002g0149 |
3 | HG03704.hp2 HG03834.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.417+542_417+545dup others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | ||||||
chr7:156655239 | GCA | G | 45 | a0001c0001t0002g0073 a0001c0001t0002g0136 a0001c0004t0006g0013 others(42): Show |
57 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.417+544_417+545del others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655239 | ||||||
chr7:156655262 | C | CAG | 3 | a0001c0001t0003g0236 a0002c0002t0001g0227 a0003c0003t0002g0189 |
3 | HG02027.hp1 HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.417+558_417+559dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655262 | ||||||
chr7:156655262 | C | G | 182 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(179): Show |
291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.417+544C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655262 | |||||||
chr7:156655293 | T | G | 101 | a0001c0001t0002g0102 a0001c0001t0002g0107 a0001c0001t0002g0110 others(98): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.417+575T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655293 | |||||||
chr7:156655295 | G | T | 50 | a0001c0001t0002g0005 a0001c0001t0002g0022 a0001c0001t0002g0040 others(47): Show |
73 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.417+577G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655295 | |||||||
chr7:156655297 | G | T | 3 | a0001c0001t0002g0156 a0001c0001t0003g0057 a0001c0001t0003g0253 |
4 | NA18948.hp2 NA18990.hp1 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+579G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655297 | |||||||
chr7:156655416 | G | A | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.417+698G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655416 | |||||||
chr7:156655421 | T | C | 1 | a0001c0001t0002g0017 | 3 | HG01243.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.417+703T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655421 | |||||||
chr7:156655424 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0116 |
3 | HG00408.hp2 HG02056.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.417+706G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655424 | |||||||
chr7:156655449 | C | T | 148 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(145): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.417+731C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655449 | |||||||
chr7:156655451 | T | C | 4 | a0002c0002t0001g0050 a0002c0002t0001g0214 a0002c0002t0001g0215 others(1): Show |
5 | HG03041.hp1 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+733T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655451 | |||||||
chr7:156655453 | G | T | 2 | a0003c0003t0004g0144 a0005c0006t0004g0021 |
4 | HG01256.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+735G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655453 | |||||||
chr7:156655609 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.417+891G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655609 | |||||||
chr7:156655747 | A | G | 1 | a0001c0001t0002g0038 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.417+1029A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655747 | |||||||
chr7:156655787 | T | TTAGTAAT others(344): Show |
1 | a0001c0001t0003g0257 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.417+1081_417+1082i others(353): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | ||||||
chr7:156655787 | T | TTAGTAAT others(345): Show |
1 | a0001c0001t0003g0258 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.417+1081_417+1082i others(354): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | ||||||
chr7:156655787 | T | TTAGTAAT others(350): Show |
1 | a0001c0001t0003g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.417+1081_417+1082i others(359): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 156655787 | ||||||
chr7:156655998 | C | T | 155 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(152): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.417+1280C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156655998 | |||||||
chr7:156656018 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+1300C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656018 | |||||||
chr7:156656520 | T | C | 1 | a0002c0002t0001g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.418-1021T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656520 | |||||||
chr7:156656566 | G | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-975G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656566 | |||||||
chr7:156656762 | A | C | 199 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(196): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.418-779A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656762 | |||||||
chr7:156656764 | C | A | 43 | a0001c0001t0002g0017 a0001c0001t0002g0262 a0001c0001t0003g0003 others(40): Show |
73 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.418-777C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656764 | |||||||
chr7:156656857 | T | C | 38 | a0001c0001t0002g0073 a0001c0004t0006g0013 a0001c0004t0006g0092 others(35): Show |
48 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.418-684T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656857 | |||||||
chr7:156656925 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.418-616T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156656925 | |||||||
chr7:156657046 | A | G | 2 | a0004c0005t0002g0059 a0004c0005t0002g0269 |
3 | HG01884.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.418-495A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657046 | |||||||
chr7:156657215 | C | G | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418-326C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657215 | |||||||
chr7:156657366 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.418-175G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657366 | |||||||
chr7:156657384 | C | T | 1 | a0003c0003t0004g0085 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418-157C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 4/8 | chr7 | 156657384 | |||||||
chr7:156657866 | C | T | 1 | a0001c0004t0002g0216 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.451-262C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 5/8 | chr7 | 156657866 | |||||||
chr7:156658269 | C | T | 1 | a0002c0002t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.575+17C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 6/8 | chr7 | 156658269 | |||||||
chr7:156658276 | C | T | 1 | a0001c0001t0002g0060 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.575+24C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 6/8 | chr7 | 156658276 | |||||||
chr7:156658652 | T | C | 1 | a0002c0002t0001g0047 | 2 | NA18971.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.684+82T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658652 | |||||||
chr7:156658740 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684+170C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658740 | |||||||
chr7:156658998 | T | C | 1 | a0011c0010t0001g0221 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.684+428T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156658998 | |||||||
chr7:156659022 | A | G | 3 | a0002c0002t0001g0077 a0003c0003t0004g0078 a0003c0003t0004g0079 |
3 | HG02258.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.684+452A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659022 | |||||||
chr7:156659066 | A | G | 5 | a0001c0001t0002g0017 a0001c0001t0003g0053 a0001c0001t0003g0248 others(2): Show |
8 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+496A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659066 | |||||||
chr7:156659114 | C | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+544C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659114 | |||||||
chr7:156659272 | A | C | 2 | a0001c0001t0003g0234 a0001c0001t0003g0236 |
2 | HG02015.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.684+702A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659272 | |||||||
chr7:156659395 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0101 a0001c0001t0002g0119 |
5 | NA18967.hp2 NA18975.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+825G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659395 | |||||||
chr7:156659512 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.684+942C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659512 | |||||||
chr7:156659534 | CATA | C | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+965_684+967del others(3): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659534 | |||||||
chr7:156659553 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+983A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659553 | |||||||
chr7:156659584 | C | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+1014C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659584 | |||||||
chr7:156659858 | T | G | 1 | a0001c0001t0002g0150 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.684+1288T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156659858 | |||||||
chr7:156660040 | A | G | 1 | a0002c0002t0001g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.684+1470A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660040 | |||||||
chr7:156660108 | C | A | 6 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(3): Show |
9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+1538C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660108 | |||||||
chr7:156660130 | G | T | 1 | a0002c0002t0001g0181 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.684+1560G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660130 | |||||||
chr7:156660559 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.684+1989G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660559 | |||||||
chr7:156660642 | T | C | 1 | a0002c0002t0001g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.684+2072T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660642 | |||||||
chr7:156660695 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2125G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660695 | |||||||
chr7:156660719 | T | G | 1 | a0002c0002t0001g0044 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.684+2149T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660719 | |||||||
chr7:156660820 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2250T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660820 | |||||||
chr7:156660821 | G | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2251G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660821 | |||||||
chr7:156660828 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.684+2258G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660828 | |||||||
chr7:156660960 | T | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0112 |
3 | HG00099.hp1 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.684+2390T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660960 | |||||||
chr7:156660966 | A | G | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+2396A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156660966 | |||||||
chr7:156661066 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+2496T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661066 | |||||||
chr7:156661074 | G | A | 1 | a0002c0002t0001g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.684+2504G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661074 | |||||||
chr7:156661116 | G | T | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+2546G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661116 | |||||||
chr7:156661146 | C | T | 2 | a0003c0003t0007g0270 a0003c0003t0007g0271 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.684+2576C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661146 | |||||||
chr7:156661210 | C | CATA | 161 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(158): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.684+2642_684+2644d others(5): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661210 | ||||||
chr7:156661240 | G | A | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+2670G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661240 | |||||||
chr7:156661298 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.684+2728C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661298 | |||||||
chr7:156661299 | G | A | 2 | a0003c0003t0002g0231 a0003c0003t0002g0232 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.684+2729G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661299 | |||||||
chr7:156661302 | C | A | 1 | a0002c0002t0001g0192 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.684+2732C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661302 | |||||||
chr7:156661322 | A | AT | 139 | a0001c0001t0002g0073 a0001c0001t0002g0106 a0001c0001t0002g0111 others(136): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.684+2767dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661322 | ||||||
chr7:156661322 | A | ATT | 10 | a0001c0004t0002g0163 a0002c0002t0001g0178 a0002c0002t0001g0179 others(7): Show |
10 | HG02738.hp1 HG02896.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+2766_684+2767d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156661322 | ||||||
chr7:156661479 | C | T | 1 | a0004c0012t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.684+2909C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661479 | |||||||
chr7:156661617 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+3047T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661617 | |||||||
chr7:156661729 | T | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+3159T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661729 | |||||||
chr7:156661786 | G | T | 1 | a0002c0002t0001g0133 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.684+3216G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156661786 | |||||||
chr7:156662011 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.684+3441T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662011 | |||||||
chr7:156662169 | G | A | 107 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(104): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.684+3599G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662169 | |||||||
chr7:156662367 | T | C | 1 | a0003c0003t0004g0034 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.684+3797T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662367 | |||||||
chr7:156662395 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.684+3825T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662395 | |||||||
chr7:156662559 | C | G | 4 | a0002c0002t0001g0230 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+3989C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662559 | |||||||
chr7:156662611 | G | A | 8 | a0003c0003t0002g0231 a0004c0005t0002g0059 a0004c0005t0002g0265 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.684+4041G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662611 | |||||||
chr7:156662631 | C | T | 33 | a0001c0001t0002g0073 a0002c0002t0001g0076 a0002c0002t0001g0077 others(30): Show |
40 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.684+4061C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156662631 | |||||||
chr7:156662847 | C | CT | 12 | a0001c0001t0002g0037 a0001c0001t0002g0107 a0001c0001t0002g0132 others(9): Show |
15 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.684+4295dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156662847 | ||||||
chr7:156662847 | CT | C | 12 | a0001c0004t0002g0163 a0002c0002t0001g0170 a0002c0002t0001g0184 others(9): Show |
13 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.684+4295delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156662847 | ||||||
chr7:156663061 | C | A | 9 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0028 others(6): Show |
20 | HG00408.hp1 HG00423.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.684+4491C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663061 | |||||||
chr7:156663157 | A | C | 154 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(151): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.684+4587A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663157 | |||||||
chr7:156663585 | C | T | 146 | a0001c0001t0002g0073 a0001c0001t0002g0186 a0001c0001t0002g0199 others(143): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.684+5015C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663585 | |||||||
chr7:156663673 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.684+5103T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663673 | |||||||
chr7:156663815 | AAAATTAT others(3): Show |
A | 1 | a0002c0002t0001g0207 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.684+5247_684+5256d others(12): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156663815 | ||||||
chr7:156663913 | C | G | 1 | a0002c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.684+5343C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663913 | |||||||
chr7:156663996 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.684+5426T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156663996 | |||||||
chr7:156664021 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+5451G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664021 | |||||||
chr7:156664043 | A | G | 194 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(191): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.684+5473A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664043 | |||||||
chr7:156664059 | G | A | 12 | a0002c0002t0001g0024 a0002c0002t0001g0027 a0002c0002t0001g0045 others(9): Show |
18 | HG02080.hp2 HG02135.hp1 NA18943.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+5489G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664059 | |||||||
chr7:156664085 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.684+5515T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664085 | |||||||
chr7:156664098 | C | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+5528C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664098 | |||||||
chr7:156664136 | G | A | 3 | a0002c0002t0001g0046 a0002c0002t0001g0175 a0002c0002t0001g0185 |
4 | HG00597.hp1 NA18960.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+5566G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664136 | |||||||
chr7:156664164 | A | G | 197 | a0001c0001t0002g0017 a0001c0001t0002g0073 a0001c0001t0002g0186 others(194): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.684+5594A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664164 | |||||||
chr7:156664183 | C | T | 1 | a0003c0003t0004g0089 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.684+5613C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664183 | |||||||
chr7:156664218 | T | C | 2 | a0002c0002t0001g0161 a0003c0003t0002g0189 |
2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.684+5648T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664218 | |||||||
chr7:156664275 | A | C | 4 | a0002c0002t0001g0010 a0002c0002t0001g0048 a0002c0002t0001g0192 others(1): Show |
8 | NA18942.hp2 NA18954.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+5705A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664275 | |||||||
chr7:156664318 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0120 |
3 | HG01261.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.684+5748G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664318 | |||||||
chr7:156664321 | C | G | 102 | a0001c0001t0002g0186 a0001c0001t0002g0199 a0001c0004t0002g0163 others(99): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.684+5751C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664321 | |||||||
chr7:156664322 | G | T | 1 | a0002c0002t0001g0205 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.684+5752G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664322 | |||||||
chr7:156664329 | C | T | 2 | a0001c0001t0002g0042 a0010c0011t0002g0042 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.684+5759C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664329 | |||||||
chr7:156664330 | G | A | 44 | a0001c0001t0002g0017 a0001c0001t0003g0003 a0001c0001t0003g0031 others(41): Show |
74 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.684+5760G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664330 | |||||||
chr7:156664333 | C | T | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+5763C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664333 | |||||||
chr7:156664375 | A | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+5805A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664375 | |||||||
chr7:156664381 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.684+5811C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664381 | |||||||
chr7:156664385 | C | T | 1 | a0002c0002t0001g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.684+5815C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664385 | |||||||
chr7:156664484 | A | T | 2 | a0004c0005t0002g0059 a0004c0005t0002g0269 |
3 | HG01884.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.684+5914A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664484 | |||||||
chr7:156664583 | T | C | 12 | a0001c0001t0002g0199 a0002c0002t0001g0008 a0002c0002t0001g0193 others(9): Show |
17 | HG00639.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+6013T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664583 | |||||||
chr7:156664739 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+6169T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664739 | |||||||
chr7:156664988 | G | A | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.684+6418G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156664988 | |||||||
chr7:156665086 | CT | C | 4 | a0001c0001t0003g0057 a0001c0001t0003g0251 a0001c0001t0003g0253 others(1): Show |
5 | NA18939.hp2 NA18948.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+6519delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156665086 | ||||||
chr7:156665314 | CT | C | 29 | a0001c0001t0002g0073 a0002c0002t0001g0076 a0003c0003t0004g0009 others(26): Show |
36 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.684+6745delT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665314 | |||||||
chr7:156665624 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+7054A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665624 | |||||||
chr7:156665641 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.684+7071A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665641 | |||||||
chr7:156665670 | CCT | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+7101_684+7102d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665670 | |||||||
chr7:156665768 | T | C | 50 | a0001c0001t0002g0073 a0001c0004t0006g0013 a0001c0004t0006g0092 others(47): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.684+7198T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665768 | |||||||
chr7:156665852 | G | T | 38 | a0001c0001t0002g0017 a0001c0001t0003g0003 a0001c0001t0003g0031 others(35): Show |
66 | HG00673.hp1 HG01243.hp1 HG01358.hp2 others(63): Show |
intron_variant | MODIFIER | c.684+7282G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665852 | |||||||
chr7:156665877 | G | C | 3 | a0001c0004t0002g0222 a0002c0002t0001g0015 a0008c0009t0001g0015 |
5 | HG00423.hp2 HG02056.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+7307G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156665877 | |||||||
chr7:156666032 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+7462A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666032 | |||||||
chr7:156666046 | T | C | 1 | a0001c0001t0003g0258 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.684+7476T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666046 | |||||||
chr7:156666061 | G | A | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.684+7491G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666061 | |||||||
chr7:156666144 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.684+7574G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666144 | |||||||
chr7:156666383 | C | G | 5 | a0002c0002t0001g0050 a0002c0002t0001g0161 a0002c0002t0001g0214 others(2): Show |
6 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+7813C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666383 | |||||||
chr7:156666510 | T | C | 5 | a0002c0002t0001g0050 a0002c0002t0001g0161 a0002c0002t0001g0214 others(2): Show |
6 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+7940T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666510 | |||||||
chr7:156666656 | G | A | 1 | a0002c0002t0001g0230 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.684+8086G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666656 | |||||||
chr7:156666680 | G | A | 19 | a0001c0001t0002g0005 a0001c0001t0002g0023 a0001c0001t0002g0040 others(16): Show |
32 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.684+8110G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666680 | |||||||
chr7:156666726 | T | G | 9 | a0001c0004t0002g0222 a0002c0002t0001g0015 a0002c0002t0001g0030 others(6): Show |
13 | HG00423.hp2 HG01069.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.684+8156T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666726 | |||||||
chr7:156666866 | T | G | 4 | a0002c0002t0001g0143 a0003c0003t0002g0052 a0003c0003t0002g0231 others(1): Show |
5 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+8296T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666866 | |||||||
chr7:156666988 | G | A | 1 | a0002c0002t0001g0200 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.684+8418G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156666988 | |||||||
chr7:156667002 | C | T | 3 | a0004c0005t0002g0059 a0004c0005t0002g0268 a0004c0005t0002g0269 |
4 | HG01884.hp1 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+8432C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667002 | |||||||
chr7:156667037 | C | G | 4 | a0001c0001t0002g0019 a0001c0001t0002g0107 a0001c0001t0002g0108 others(1): Show |
6 | HG00140.hp1 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+8467C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667037 | |||||||
chr7:156667341 | T | A | 1 | a0003c0003t0004g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.685-8355T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667341 | |||||||
chr7:156667348 | A | T | 1 | a0003c0003t0004g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-8348A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667348 | |||||||
chr7:156667491 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-8205T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667491 | |||||||
chr7:156667510 | T | C | 3 | a0003c0003t0002g0052 a0003c0003t0002g0231 a0003c0003t0002g0232 |
4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-8186T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667510 | |||||||
chr7:156667561 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.685-8135A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667561 | |||||||
chr7:156667665 | ACACGGAA others(9): Show |
A | 1 | a0001c0001t0002g0121 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.685-8030_685-8015d others(18): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667665 | |||||||
chr7:156667737 | A | G | 7 | a0001c0004t0006g0013 a0001c0004t0006g0093 a0001c0004t0006g0094 others(4): Show |
10 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-7959A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667737 | |||||||
chr7:156667769 | G | C | 1 | a0002c0002t0001g0201 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.685-7927G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667769 | |||||||
chr7:156667820 | C | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(48): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.685-7876C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667820 | |||||||
chr7:156667866 | A | C | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-7830A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667866 | |||||||
chr7:156667920 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.685-7776G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667920 | |||||||
chr7:156667925 | A | G | 10 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(7): Show |
15 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-7771A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156667925 | |||||||
chr7:156668051 | C | G | 8 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(5): Show |
12 | HG02280.hp1 HG02559.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-7645C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668051 | |||||||
chr7:156668077 | A | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-7619A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668077 | |||||||
chr7:156668157 | A | C | 3 | a0001c0001t0003g0031 a0001c0001t0003g0234 a0001c0004t0002g0222 |
5 | HG02015.hp2 HG02074.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-7539A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668157 | |||||||
chr7:156668174 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.685-7522G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668174 | |||||||
chr7:156668360 | T | C | 1 | a0002c0002t0001g0273 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.685-7336T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668360 | |||||||
chr7:156668488 | C | A | 103 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(100): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.685-7208C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668488 | |||||||
chr7:156668491 | C | CAGTGACT others(11): Show |
1 | a0001c0001t0002g0121 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.685-7204_685-7187d others(20): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156668491 | ||||||
chr7:156668513 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-7183T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668513 | |||||||
chr7:156668521 | C | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-7175C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668521 | |||||||
chr7:156668535 | C | T | 3 | a0003c0003t0002g0189 a0003c0003t0007g0270 a0003c0003t0007g0271 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-7161C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668535 | |||||||
chr7:156668568 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.685-7128C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668568 | |||||||
chr7:156668596 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.685-7100G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668596 | |||||||
chr7:156668654 | G | A | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-7042G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668654 | |||||||
chr7:156668684 | A | G | 7 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(4): Show |
10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-7012A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668684 | |||||||
chr7:156668687 | G | A | 1 | a0003c0003t0004g0049 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.685-7009G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668687 | |||||||
chr7:156668773 | T | C | 1 | a0003c0003t0004g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.685-6923T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668773 | |||||||
chr7:156668774 | G | A | 2 | a0003c0003t0004g0086 a0003c0003t0004g0091 |
2 | NA19054.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.685-6922G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668774 | |||||||
chr7:156668928 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.685-6768T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156668928 | |||||||
chr7:156669178 | A | G | 1 | a0002c0002t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-6518A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669178 | |||||||
chr7:156669215 | G | A | 2 | a0003c0003t0004g0081 a0006c0008t0002g0033 |
3 | HG02683.hp1 HG02698.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.685-6481G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669215 | |||||||
chr7:156669248 | G | T | 7 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(4): Show |
10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-6448G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669248 | |||||||
chr7:156669264 | G | A | 37 | a0001c0001t0002g0186 a0002c0002t0001g0076 a0003c0003t0004g0009 others(34): Show |
47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-6432G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669264 | |||||||
chr7:156669266 | A | G | 45 | a0001c0001t0002g0186 a0001c0004t0006g0013 a0001c0004t0006g0092 others(42): Show |
58 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.685-6430A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669266 | |||||||
chr7:156669273 | G | A | 1 | a0002c0002t0001g0025 | 3 | NA18953.hp2 NA18973.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.685-6423G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669273 | |||||||
chr7:156669409 | G | A | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-6287G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669409 | |||||||
chr7:156669412 | G | A | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-6284G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669412 | |||||||
chr7:156669537 | G | A | 1 | a0002c0002t0001g0173 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.685-6159G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669537 | |||||||
chr7:156669641 | C | G | 2 | a0001c0004t0002g0163 a0001c0004t0002g0216 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-6055C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669641 | |||||||
chr7:156669670 | A | G | 14 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(11): Show |
18 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.685-6026A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669670 | |||||||
chr7:156669742 | G | A | 1 | a0004c0005t0002g0268 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.685-5954G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669742 | |||||||
chr7:156669884 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.685-5812C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669884 | |||||||
chr7:156669886 | G | A | 5 | a0003c0003t0004g0066 a0003c0003t0004g0071 a0003c0003t0004g0080 others(2): Show |
5 | HG00438.hp2 NA18998.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-5810G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669886 | |||||||
chr7:156669888 | A | G | 1 | a0002c0002t0001g0207 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.685-5808A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669888 | |||||||
chr7:156669934 | C | T | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-5762C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669934 | |||||||
chr7:156669968 | A | T | 3 | a0002c0002t0005g0241 a0002c0002t0005g0242 a0002c0002t0005g0254 |
3 | NA18944.hp1 NA18968.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.685-5728A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156669968 | |||||||
chr7:156670051 | T | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5645T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670051 | |||||||
chr7:156670096 | C | T | 105 | a0001c0004t0002g0222 a0002c0002t0001g0002 a0002c0002t0001g0004 others(102): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.685-5600C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670096 | |||||||
chr7:156670163 | C | T | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5533C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670163 | |||||||
chr7:156670255 | C | T | 3 | a0001c0004t0002g0222 a0002c0002t0001g0015 a0008c0009t0001g0015 |
5 | HG00423.hp2 HG02056.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-5441C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670255 | |||||||
chr7:156670327 | G | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-5369G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670327 | |||||||
chr7:156670328 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.685-5368G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670328 | |||||||
chr7:156670599 | C | T | 1 | a0002c0002t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.685-5097C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670599 | |||||||
chr7:156670677 | G | A | 2 | a0001c0004t0002g0163 a0001c0004t0002g0216 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-5019G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670677 | |||||||
chr7:156670932 | C | T | 3 | a0002c0002t0001g0012 a0002c0002t0001g0213 a0002c0002t0001g0230 |
7 | HG01952.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-4764C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156670932 | |||||||
chr7:156671064 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-4632C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671064 | |||||||
chr7:156671134 | A | G | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-4562A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671134 | |||||||
chr7:156671286 | T | C | 182 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(179): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.685-4410T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671286 | |||||||
chr7:156671395 | G | A | 181 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(178): Show |
298 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.685-4301G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671395 | |||||||
chr7:156671417 | G | A | 225 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(222): Show |
353 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.685-4279G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671417 | |||||||
chr7:156671452 | A | G | 1 | a0001c0004t0002g0163 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.685-4244A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671452 | |||||||
chr7:156671520 | T | C | 60 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(57): Show |
98 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.685-4176T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671520 | |||||||
chr7:156671534 | A | T | 106 | a0001c0004t0002g0222 a0002c0002t0001g0002 a0002c0002t0001g0004 others(103): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.685-4162A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671534 | |||||||
chr7:156671587 | A | C | 14 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(11): Show |
18 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.685-4109A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671587 | |||||||
chr7:156671645 | A | G | 71 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(68): Show |
112 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.685-4051A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671645 | |||||||
chr7:156671652 | T | C | 1 | a0003c0003t0004g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.685-4044T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671652 | |||||||
chr7:156671656 | T | TGCGGTAC others(53): Show |
1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-4031_685-4030i others(62): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156671656 | ||||||
chr7:156671666 | G | A | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-4030G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671666 | |||||||
chr7:156671698 | C | G | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-3998C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671698 | |||||||
chr7:156671720 | C | T | 2 | a0001c0004t0002g0163 a0001c0004t0002g0216 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-3976C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671720 | |||||||
chr7:156671756 | C | T | 1 | a0003c0003t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.685-3940C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671756 | |||||||
chr7:156671765 | T | G | 9 | a0002c0002t0001g0046 a0002c0002t0001g0175 a0002c0002t0001g0183 others(6): Show |
11 | HG00597.hp1 NA18940.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-3931T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671765 | |||||||
chr7:156671773 | T | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-3923T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671773 | |||||||
chr7:156671817 | G | A | 164 | a0001c0001t0002g0186 a0001c0004t0006g0013 a0001c0004t0006g0092 others(161): Show |
254 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.685-3879G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671817 | |||||||
chr7:156671840 | A | AT | 104 | a0001c0004t0002g0222 a0002c0002t0001g0002 a0002c0002t0001g0004 others(101): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.685-3848dupT | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156671840 | ||||||
chr7:156671848 | T | A | 3 | a0003c0003t0002g0052 a0003c0003t0002g0231 a0003c0003t0002g0232 |
4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-3848T>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671848 | |||||||
chr7:156671849 | A | T | 5 | a0001c0004t0006g0094 a0002c0002t0005g0240 a0003c0003t0002g0189 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-3847A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671849 | |||||||
chr7:156671884 | G | A | 184 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(181): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.685-3812G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156671884 | |||||||
chr7:156672045 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.685-3651G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672045 | |||||||
chr7:156672045 | GA | G | 20 | a0001c0001t0002g0005 a0001c0001t0002g0023 a0001c0001t0002g0040 others(17): Show |
33 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.685-3649delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156672045 | ||||||
chr7:156672488 | C | G | 1 | a0001c0001t0003g0251 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.685-3208C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672488 | |||||||
chr7:156672515 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.685-3181T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672515 | |||||||
chr7:156672660 | A | G | 3 | a0003c0003t0004g0078 a0003c0003t0004g0079 a0005c0006t0004g0021 |
5 | HG02258.hp1 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-3036A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672660 | |||||||
chr7:156672666 | G | A | 3 | a0003c0003t0002g0189 a0003c0003t0007g0270 a0003c0003t0007g0271 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-3030G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672666 | |||||||
chr7:156672736 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-2960T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672736 | |||||||
chr7:156672821 | G | A | 1 | a0002c0002t0001g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.685-2875G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672821 | |||||||
chr7:156672987 | C | T | 1 | a0011c0010t0001g0221 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.685-2709C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156672987 | |||||||
chr7:156673002 | A | G | 225 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(222): Show |
353 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.685-2694A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673002 | |||||||
chr7:156673528 | G | T | 1 | a0003c0003t0004g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-2168G>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673528 | |||||||
chr7:156673543 | T | C | 1 | a0006c0008t0002g0033 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.685-2153T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673543 | |||||||
chr7:156673548 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.685-2148C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673548 | |||||||
chr7:156673631 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.685-2065C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673631 | |||||||
chr7:156673684 | C | T | 31 | a0001c0001t0002g0186 a0002c0002t0001g0076 a0003c0003t0004g0009 others(28): Show |
39 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.685-2012C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673684 | |||||||
chr7:156673906 | T | TAA | 6 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(3): Show |
9 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-1775_685-1774d others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | ||||||
chr7:156673906 | T | TAAAAA | 6 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1778_685-1774d others(7): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | ||||||
chr7:156673906 | TA | T | 60 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(57): Show |
98 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.685-1774delA | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673906 | ||||||
chr7:156673907 | A | T | 3 | a0003c0003t0002g0052 a0003c0003t0002g0231 a0003c0003t0002g0232 |
4 | HG02717.hp2 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-1789A>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673907 | |||||||
chr7:156673915 | A | AAG | 5 | a0002c0002t0001g0045 a0002c0002t0001g0051 a0002c0002t0001g0171 others(2): Show |
7 | NA18522.hp2 NA18943.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-1780_685-1779i others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673915 | ||||||
chr7:156673918 | A | G | 59 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(56): Show |
97 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.685-1778A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673918 | |||||||
chr7:156673919 | A | AAG | 100 | a0001c0004t0002g0222 a0002c0002t0001g0002 a0002c0002t0001g0004 others(97): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.685-1776_685-1775i others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156673919 | ||||||
chr7:156673919 | A | G | 5 | a0002c0002t0001g0045 a0002c0002t0001g0051 a0002c0002t0001g0171 others(2): Show |
7 | NA18522.hp2 NA18943.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-1777A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673919 | |||||||
chr7:156673922 | AG | A | 37 | a0001c0001t0002g0186 a0002c0002t0001g0076 a0003c0003t0004g0009 others(34): Show |
47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-1773delG | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673922 | |||||||
chr7:156673925 | A | G | 37 | a0001c0001t0002g0186 a0002c0002t0001g0076 a0003c0003t0004g0009 others(34): Show |
47 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.685-1771A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673925 | |||||||
chr7:156673985 | A | C | 1 | a0002c0002t0001g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-1711A>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156673985 | |||||||
chr7:156674072 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685-1624C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674072 | |||||||
chr7:156674105 | G | A | 3 | a0001c0001t0002g0102 a0001c0001t0002g0153 a0002c0002t0001g0224 |
3 | HG00280.hp2 HG02451.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.685-1591G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674105 | |||||||
chr7:156674166 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.685-1530G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674166 | |||||||
chr7:156674226 | G | A | 8 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(5): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.685-1470G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674226 | |||||||
chr7:156674518 | G | A | 3 | a0003c0003t0002g0189 a0003c0003t0007g0270 a0003c0003t0007g0271 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-1178G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674518 | |||||||
chr7:156674531 | G | A | 24 | a0001c0001t0002g0073 a0001c0001t0002g0136 a0001c0001t0003g0003 others(21): Show |
43 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.685-1165G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674531 | |||||||
chr7:156674547 | T | C | 185 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0022 others(182): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.685-1149T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674547 | |||||||
chr7:156674548 | G | A | 1 | a0002c0002t0001g0227 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.685-1148G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674548 | |||||||
chr7:156674601 | G | A | 1 | a0002c0002t0001g0048 | 2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.685-1095G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674601 | |||||||
chr7:156674624 | T | C | 7 | a0004c0005t0002g0059 a0004c0005t0002g0265 a0004c0005t0002g0266 others(4): Show |
8 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-1072T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674624 | |||||||
chr7:156674660 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0132 |
3 | HG00438.hp1 HG02080.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.685-1036C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674660 | |||||||
chr7:156674729 | C | T | 1 | a0001c0001t0002g0036 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.685-967C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674729 | |||||||
chr7:156674730 | G | A | 1 | a0002c0002t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.685-966G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674730 | |||||||
chr7:156674811 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.685-885T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156674811 | |||||||
chr7:156675016 | G | C | 1 | a0002c0002t0001g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.685-680G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675016 | |||||||
chr7:156675032 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-664G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675032 | |||||||
chr7:156675070 | G | A | 58 | a0001c0001t0002g0186 a0001c0004t0006g0013 a0001c0004t0006g0092 others(55): Show |
74 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.685-626G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675070 | |||||||
chr7:156675115 | AGACCCGA others(12): Show |
A | 1 | a0001c0001t0002g0140 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.685-571_685-553del others(19): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr7 | 156675115 | ||||||
chr7:156675134 | C | A | 205 | a0001c0001t0002g0017 a0001c0001t0002g0022 a0001c0001t0002g0073 others(202): Show |
320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.685-562C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675134 | |||||||
chr7:156675227 | A | G | 20 | a0001c0004t0002g0163 a0001c0004t0003g0247 a0001c0004t0006g0013 others(17): Show |
25 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.685-469A>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675227 | |||||||
chr7:156675379 | G | A | 1 | a0003c0003t0004g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.685-317G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675379 | |||||||
chr7:156675500 | G | A | 1 | a0001c0004t0003g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.685-196G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675500 | |||||||
chr7:156675683 | G | A | 1 | a0002c0002t0005g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.685-13G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675683 | |||||||
chr7:156675683 | G | C | 162 | a0001c0004t0003g0247 a0001c0004t0006g0013 a0001c0004t0006g0092 others(159): Show |
252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.685-13G>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675683 | |||||||
chr7:156675684 | C | A | 102 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(99): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.685-12C>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675684 | |||||||
chr7:156675684 | C | T | 7 | a0001c0004t0006g0013 a0001c0004t0006g0092 a0001c0004t0006g0093 others(4): Show |
10 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-12C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675684 | |||||||
chr7:156675685 | C | G | 3 | a0003c0003t0002g0189 a0003c0003t0007g0270 a0003c0003t0007g0271 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685-11C>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675685 | |||||||
chr7:156675685 | C | T | 1 | a0002c0002t0005g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.685-11C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 7/8 | chr7 | 156675685 | |||||||
chr7:156675865 | T | C | 44 | a0002c0002t0001g0076 a0003c0003t0002g0052 a0003c0003t0002g0189 others(41): Show |
55 | HG00438.hp2 HG00609.hp2 HG01168.hp2 others(52): Show |
splice_donor_variant&intron_variant | HIGH | c.852+2T>C | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675865 | |||||||
chr7:156675916 | G | A | 1 | a0002c0002t0001g0176 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.852+53G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675916 | |||||||
chr7:156675962 | G | A | 116 | a0001c0001t0003g0235 a0002c0002t0001g0002 a0002c0002t0001g0004 others(113): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.852+99G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675962 | |||||||
chr7:156675962 | G | GAGCCTAG others(76): Show |
1 | a0001c0004t0003g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.852+130_852+131ins others(83): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156675962 | ||||||
chr7:156675971 | A | AGTGTCAG others(61): Show |
1 | a0001c0001t0002g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.852+109_852+176dup others(68): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156675971 | ||||||
chr7:156675994 | G | A | 8 | a0001c0004t0003g0247 a0001c0004t0006g0013 a0001c0004t0006g0092 others(5): Show |
11 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.852+131G>A | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156675994 | |||||||
chr7:156676062 | T | G | 207 | a0001c0001t0002g0017 a0001c0001t0002g0022 a0001c0001t0002g0073 others(204): Show |
322 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.852+199T>G | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676062 | |||||||
chr7:156676065 | C | T | 109 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(106): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.852+202C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676065 | |||||||
chr7:156676245 | G | GTA | 8 | a0001c0004t0003g0247 a0001c0004t0006g0013 a0001c0004t0006g0092 others(5): Show |
11 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-164_853-163dup others(2): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156676245 | ||||||
chr7:156676245 | G | GTGTA | 110 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(107): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.853-173_853-172ins others(4): Show |
RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 156676245 | ||||||
chr7:156676402 | C | T | 118 | a0001c0001t0002g0019 a0001c0001t0002g0037 a0001c0001t0002g0100 others(115): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.853-17C>T | RNF32 | ENSG00000105982.17 | transcript | ENST00000317955.10 | protein_coding | 8/8 | chr7 | 156676402 |