Item | Value |
---|---|
geneid | 101929355 |
ensemblid | ENSG00000283361.3 |
hgncid | 53789 |
symbol | CFAP97D2 |
name | CFAP97 domain containing 2 |
refseq_nuc | NM_001395229.1 |
refseq_prot | NP_001382158.1 |
ensembl_nuc | ENST00000636692.2 |
ensembl_prot | ENSP00000489989.1 |
mane_status | MANE Select |
chr | chr13 |
start | 114179257 |
end | 114223085 |
strand | + |
ver | v1.2 |
region | chr13:114179257-114223085 |
region5000 | chr13:114174257-114228085 |
regionname0 | CFAP97D2_chr13_114179257_114223085 |
regionname5000 | CFAP97D2_chr13_114174257_114228085 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 98 | 399 | 94 | 78 | 175 | 10 | 40 | 137 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | MHGAP others(93): Show |
chr13 | 114174257 | 114228085 |
a0002 | 0/0 | 98 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | MHGAP others(93): Show |
chr13 | 114174257 | 114228085 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 294 | 396 | 92 | 77 | 175 | 10 | 40 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ATGCA others(289): Show |
chr13 | 114174257 | 114228085 | ||
a0001c0002 | 0/0 | 294 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ATGCA others(289): Show |
chr13 | 114174257 | 114228085 | ||
a0001c0004 | 0/0 | 294 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ATGCA others(289): Show |
chr13 | 114174257 | 114228085 | ||
a0002c0003 | 0/0 | 294 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ATGCA others(289): Show |
chr13 | 114174257 | 114228085 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 949 | 152 | 67 | 32 | 26 | 5 | 21 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0002 | 1/0 | 949 | 79 | 4 | 25 | 36 | 4 | 9 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0003 | 0/0 | 949 | 75 | 1 | 6 | 62 | 0 | 6 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0004 | 0/0 | 949 | 35 | 0 | 2 | 31 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0005 | 0/0 | 958 | 23 | 13 | 2 | 8 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(953): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0006 | 0/0 | 958 | 15 | 0 | 7 | 7 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(953): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0007 | 0/0 | 958 | 7 | 4 | 1 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(953): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0008 | 0/0 | 949 | 4 | 1 | 1 | 0 | 1 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0009 | 0/0 | 949 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0010 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0011 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0012 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0001t0013 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0002t0001 | 0/0 | 949 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0001c0004t0001 | 0/0 | 949 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
a0002c0003t0001 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | ACAGC others(944): Show |
chr13 | 114174257 | 114228085 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0010g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0012g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0001t0013g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0090 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0278 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | FIN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0117 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01169 | hp2 | a0001 | c0001 | t0010 | g0317 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0333 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0324 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0234 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01993 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0336 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0338 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0330 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02129 | hp2 | a0001 | c0001 | t0013 | g0109 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02273 | hp1 | a0001 | c0001 | t0006 | g0339 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0329 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0328 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0091 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0325 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0013 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0104 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | CHB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0334 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0335 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18999 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19001 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19066 | hp2 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19084 | hp2 | a0001 | c0001 | t0012 | g0320 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0332 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19089 | hp2 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0246 | REF | REF | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0308 | REF | REF | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:114196436 | T | C | 1 | a0002 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.131T>C | p.Leu44Pro | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 205/949 | 131/297 | 44/98 | chr13 | 114196436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:114196434 | G | A | 1 | a0001c0002 | 2 | HG00733.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.129G>A | p.Pro43Pro | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 203/949 | 129/297 | 43/98 | chr13 | 114196434 | |||
chr13:114196440 | G | A | 1 | a0001c0004 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.135G>A | p.Thr45Thr | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 209/949 | 135/297 | 45/98 | chr13 | 114196440 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:114179266 | C | T | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0013 |
28 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 65 | chr13 | 114179266 | ||||||
chr13:114179306 | T | G | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 25 | chr13 | 114179306 | ||||||
chr13:114179310 | C | T | 1 | a0001c0001t0006 | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-21C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 21 | chr13 | 114179310 | ||||||
chr13:114222557 | A | C | 1 | a0001c0001t0011 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 50 | chr13 | 114222557 | ||||||
chr13:114222561 | A | ACAGATTC others(2): Show |
3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*55insCAGATTCA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 55 | chr13 | 114222561 | ||||||
chr13:114222562 | G | A | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 55 | chr13 | 114222562 | ||||||
chr13:114222602 | G | A | 3 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0013 |
37 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*95G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 95 | chr13 | 114222602 | ||||||
chr13:114222619 | A | G | 1 | a0001c0001t0009 | 2 | HG02818.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*112A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 112 | chr13 | 114222619 | ||||||
chr13:114222669 | C | T | 2 | a0001c0001t0003 a0001c0001t0011 |
76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 162 | chr13 | 114222669 | ||||||
chr13:114222709 | C | T | 1 | a0001c0001t0006 | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*202C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 202 | chr13 | 114222709 | ||||||
chr13:114222921 | G | T | 1 | a0001c0001t0010 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 414 | chr13 | 114222921 | ||||||
chr13:114222922 | T | G | 1 | a0001c0001t0010 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 415 | chr13 | 114222922 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:114179436 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.90+16A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179436 | |||||||
chr13:114179460 | C | T | 1 | a0001c0001t0003g0340 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.90+40C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179460 | |||||||
chr13:114179515 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0341 others(1): Show |
4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+95G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179515 | |||||||
chr13:114179626 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+206C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179626 | |||||||
chr13:114179626 | CT | C | 8 | a0001c0001t0001g0046 a0001c0001t0002g0049 a0001c0001t0002g0050 others(5): Show |
8 | HG01496.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+218delT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114179626 | ||||||
chr13:114179756 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG02165.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.90+336C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179756 | |||||||
chr13:114179894 | A | C | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+474A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179894 | |||||||
chr13:114179921 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(7): Show |
13 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+501G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179921 | |||||||
chr13:114179941 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.90+521G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179941 | |||||||
chr13:114180080 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+660C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180080 | |||||||
chr13:114180170 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+750A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180170 | |||||||
chr13:114180268 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+848A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180268 | |||||||
chr13:114180364 | G | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+944G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180364 | |||||||
chr13:114180392 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(245): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.90+972G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180392 | |||||||
chr13:114180445 | C | T | 1 | a0001c0001t0007g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.90+1025C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180445 | |||||||
chr13:114180464 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1044A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180464 | |||||||
chr13:114180471 | T | C | 1 | a0001c0001t0003g0015 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.90+1051T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180471 | |||||||
chr13:114180497 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(260): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.90+1077T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180497 | |||||||
chr13:114180516 | C | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.90+1096C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180516 | |||||||
chr13:114180566 | G | A | 1 | a0001c0004t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.90+1146G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180566 | |||||||
chr13:114180621 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+1201C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180621 | |||||||
chr13:114180635 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+1215C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180635 | |||||||
chr13:114180671 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.90+1251T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180671 | |||||||
chr13:114180868 | G | A | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.90+1448G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180868 | |||||||
chr13:114180996 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1576T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180996 | |||||||
chr13:114181099 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0326 |
2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.90+1679C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181099 | |||||||
chr13:114181155 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+1735T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181155 | |||||||
chr13:114181217 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0046 others(48): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.90+1797C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181217 | |||||||
chr13:114181285 | A | T | 1 | a0001c0001t0001g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+1865A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181285 | |||||||
chr13:114181383 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.90+1963A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181383 | |||||||
chr13:114181418 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1998C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181418 | |||||||
chr13:114181481 | C | T | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.90+2061C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181481 | |||||||
chr13:114181495 | C | A | 1 | a0001c0001t0002g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.90+2075C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181495 | |||||||
chr13:114181512 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+2092C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181512 | |||||||
chr13:114181541 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
36 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.90+2121C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181541 | |||||||
chr13:114181717 | T | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | NA18966.hp2 NA18973.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.90+2297T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181717 | |||||||
chr13:114181717 | T | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(55): Show |
66 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.90+2297T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181717 | |||||||
chr13:114181839 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.90+2419C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181839 | |||||||
chr13:114181918 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.90+2498G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181918 | |||||||
chr13:114181919 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.90+2499T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181919 | |||||||
chr13:114181963 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+2543C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181963 | |||||||
chr13:114181979 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(39): Show |
47 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.90+2559G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181979 | |||||||
chr13:114181983 | T | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0081 others(3): Show |
8 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+2563T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181983 | |||||||
chr13:114181993 | A | G | 2 | a0001c0001t0002g0323 a0001c0001t0002g0324 |
2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.90+2573A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181993 | |||||||
chr13:114181997 | A | G | 73 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0192 others(70): Show |
83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.90+2577A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181997 | |||||||
chr13:114182011 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0029 others(112): Show |
128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.90+2591T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182011 | |||||||
chr13:114182032 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.90+2612G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182032 | |||||||
chr13:114182043 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.90+2623T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182043 | |||||||
chr13:114182059 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2639C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182059 | |||||||
chr13:114182060 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0003g0195 |
3 | HG01243.hp1 NA18906.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.90+2640A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182060 | |||||||
chr13:114182068 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+2648T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182068 | |||||||
chr13:114182079 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.90+2659C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182079 | |||||||
chr13:114182082 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.90+2662C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182082 | |||||||
chr13:114182095 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.90+2675T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182095 | |||||||
chr13:114182126 | A | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.90+2706A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182126 | |||||||
chr13:114182128 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.90+2708T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182128 | |||||||
chr13:114182129 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2709A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182129 | |||||||
chr13:114182131 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2711T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182131 | |||||||
chr13:114182137 | A | G | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+2717A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182137 | |||||||
chr13:114182160 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0235 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+2740G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182160 | |||||||
chr13:114182164 | G | A | 1 | a0001c0001t0006g0330 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2744G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182164 | |||||||
chr13:114182168 | A | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0034 others(51): Show |
68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.90+2748A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182168 | |||||||
chr13:114182170 | A | AC | 9 | a0001c0001t0001g0059 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
9 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.90+2750_90+2751ins others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182170 | |||||||
chr13:114182170 | A | C | 1 | a0001c0001t0006g0330 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2750A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182170 | |||||||
chr13:114182172 | C | CAT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0034 others(54): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.90+2752_90+2753ins others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182172 | |||||||
chr13:114182172 | C | CGT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2754_90+2755dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114182172 | ||||||
chr13:114182172 | C | T | 11 | a0001c0001t0001g0059 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG01243.hp1 HG02040.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+2752C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182172 | |||||||
chr13:114182181 | A | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0222 others(42): Show |
57 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.90+2761A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182181 | |||||||
chr13:114182185 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(234): Show |
275 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.90+2765G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182185 | |||||||
chr13:114182189 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
68 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.90+2769A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182189 | |||||||
chr13:114182190 | T | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0198 |
2 | HG03195.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.90+2770T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182190 | |||||||
chr13:114182191 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0006g0330 |
2 | HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2771G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182191 | |||||||
chr13:114182194 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(79): Show |
103 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.90+2774G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182194 | |||||||
chr13:114182196 | A | G | 1 | a0001c0001t0006g0330 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2776A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182196 | |||||||
chr13:114182199 | T | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0085 others(6): Show |
10 | HG02886.hp1 HG02886.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2779T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182199 | |||||||
chr13:114182200 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
6 | HG01243.hp1 HG01496.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+2780A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182200 | |||||||
chr13:114182201 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): Show |
69 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.90+2781A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182201 | |||||||
chr13:114182205 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0235 a0001c0001t0002g0314 |
3 | HG00733.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+2785C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182205 | |||||||
chr13:114182206 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.90+2786A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182206 | |||||||
chr13:114182211 | A | G | 90 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0058 others(87): Show |
101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.90+2791A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182211 | |||||||
chr13:114182213 | G | A | 2 | a0001c0001t0002g0272 a0001c0001t0006g0330 |
2 | HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2793G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182213 | |||||||
chr13:114182214 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0089 a0001c0001t0001g0205 |
3 | HG01109.hp1 HG03195.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.90+2794G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182214 | |||||||
chr13:114182216 | AC | A | 69 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0051 others(66): Show |
77 | HG00621.hp1 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.90+2797delC | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182216 | |||||||
chr13:114182222 | C | A | 48 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0065 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.90+2802C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182222 | |||||||
chr13:114182225 | G | A | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0131 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2805G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182225 | |||||||
chr13:114182226 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.90+2806G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182226 | |||||||
chr13:114182228 | T | C | 47 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0051 others(44): Show |
49 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.90+2808T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182228 | |||||||
chr13:114182229 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01346.hp2 HG01496.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+2809G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182229 | |||||||
chr13:114182230 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0002g0272 |
3 | HG03098.hp1 HG03209.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2810T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182230 | |||||||
chr13:114182231 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0002g0280 a0001c0001t0002g0281 others(1): Show |
4 | HG01243.hp1 HG01346.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+2811G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182231 | |||||||
chr13:114182232 | C | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | HG01433.hp1 HG01981.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2812C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182232 | |||||||
chr13:114182234 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+2814C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182234 | |||||||
chr13:114182235 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.90+2815G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182235 | |||||||
chr13:114182235 | G | T | 1 | a0001c0001t0006g0330 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2815G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182235 | |||||||
chr13:114182236 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0206 |
2 | HG02615.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.90+2816T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182236 | |||||||
chr13:114182237 | A | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG01243.hp1 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2817A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182237 | |||||||
chr13:114182238 | G | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0029 others(62): Show |
72 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.90+2818G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182238 | |||||||
chr13:114182239 | G | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0077 others(18): Show |
25 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.90+2819G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182239 | |||||||
chr13:114182242 | A | G | 1 | a0001c0001t0005g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+2822A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182242 | |||||||
chr13:114182256 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
7 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+2836C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182256 | |||||||
chr13:114182257 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2837T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182257 | |||||||
chr13:114182259 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0004g0234 a0001c0001t0004g0262 |
3 | HG01258.hp2 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.90+2839C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182259 | |||||||
chr13:114182260 | G | A | 158 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(155): Show |
178 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.90+2840G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182260 | |||||||
chr13:114182262 | C | T | 10 | a0001c0001t0001g0114 a0001c0001t0001g0202 a0001c0001t0005g0018 others(7): Show |
12 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+2842C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182262 | |||||||
chr13:114182265 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0005g0102 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.90+2845A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182265 | |||||||
chr13:114182275 | T | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0064 others(9): Show |
12 | HG00735.hp2 HG01081.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+2855T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182275 | |||||||
chr13:114182278 | A | C | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0112 others(4): Show |
7 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2858A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182278 | |||||||
chr13:114182279 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0112 others(4): Show |
7 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2859G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182279 | |||||||
chr13:114182293 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0064 a0001c0001t0007g0266 |
3 | HG00735.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.90+2873G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182293 | |||||||
chr13:114182298 | C | T | 7 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(4): Show |
7 | HG02129.hp2 HG02132.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+2878C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182298 | |||||||
chr13:114182302 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0002g0284 |
3 | HG01081.hp2 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.90+2882A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182302 | |||||||
chr13:114182306 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.90+2886C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182306 | |||||||
chr13:114182325 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0007g0121 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2905G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182325 | |||||||
chr13:114182331 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0205 a0001c0001t0001g0207 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2911G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182331 | |||||||
chr13:114182335 | T | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0003g0154 others(2): Show |
5 | HG00621.hp1 HG00741.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+2915T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182335 | |||||||
chr13:114182335 | T | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0316 a0001c0001t0002g0286 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+2915T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182335 | |||||||
chr13:114182339 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0002g0286 a0001c0001t0008g0104 |
3 | HG02602.hp1 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.90+2919T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182339 | |||||||
chr13:114182341 | T | G | 1 | a0001c0001t0002g0287 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.90+2921T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182341 | |||||||
chr13:114182344 | C | A | 1 | a0001c0001t0002g0287 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.90+2924C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182344 | |||||||
chr13:114182346 | T | G | 3 | a0001c0001t0001g0199 a0001c0001t0002g0286 a0001c0001t0008g0104 |
3 | HG02602.hp1 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.90+2926T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182346 | |||||||
chr13:114182353 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2933G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182353 | |||||||
chr13:114182370 | A | G | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+2950A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182370 | |||||||
chr13:114182374 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.90+2954G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182374 | |||||||
chr13:114182385 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0137 |
2 | HG02647.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.90+2965C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182385 | |||||||
chr13:114182386 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2966G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182386 | |||||||
chr13:114182398 | T | C | 1 | a0001c0001t0005g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.90+2978T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182398 | |||||||
chr13:114182412 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2992A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182412 | |||||||
chr13:114182414 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2994G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182414 | |||||||
chr13:114182420 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182420 | |||||||
chr13:114182425 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.90+3005C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182425 | |||||||
chr13:114182432 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+3012T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182432 | |||||||
chr13:114182444 | A | T | 14 | a0001c0001t0003g0015 a0001c0001t0003g0118 a0001c0001t0003g0182 others(11): Show |
18 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.90+3024A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182444 | |||||||
chr13:114182450 | C | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3030C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182450 | |||||||
chr13:114182451 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3031C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182451 | |||||||
chr13:114182451 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.90+3031C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182451 | |||||||
chr13:114182452 | T | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3032T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182452 | |||||||
chr13:114182454 | C | T | 28 | a0001c0001t0001g0101 a0001c0001t0005g0018 a0001c0001t0005g0019 others(25): Show |
31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.90+3034C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182454 | |||||||
chr13:114182461 | T | G | 108 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0085 others(105): Show |
123 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.90+3041T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182461 | |||||||
chr13:114182464 | T | C | 2 | a0001c0001t0001g0138 a0001c0004t0001g0060 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.90+3044T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182464 | |||||||
chr13:114182465 | A | C | 1 | a0001c0001t0001g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+3045A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182465 | |||||||
chr13:114182466 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+3046A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182466 | |||||||
chr13:114182467 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0316 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3047T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182467 | |||||||
chr13:114182470 | A | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0316 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3050A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182470 | |||||||
chr13:114182472 | C | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG03704.hp2 HG03831.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3052C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182472 | |||||||
chr13:114182475 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90+3055A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182475 | |||||||
chr13:114182490 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3070C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182490 | |||||||
chr13:114182491 | C | G | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0138 others(7): Show |
10 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+3071C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182491 | |||||||
chr13:114182494 | T | A | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3074T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182494 | |||||||
chr13:114182496 | T | C | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0331 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3076T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182496 | |||||||
chr13:114182498 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3078G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182498 | |||||||
chr13:114182505 | G | A | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0331 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3085G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182505 | |||||||
chr13:114182507 | T | G | 30 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0087 others(27): Show |
34 | HG00408.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.90+3087T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182507 | |||||||
chr13:114182510 | A | G | 16 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0087 others(13): Show |
17 | HG00408.hp2 HG00733.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3090A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182510 | |||||||
chr13:114182528 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0087 others(11): Show |
15 | HG00408.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3108C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182528 | |||||||
chr13:114182531 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3111C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182531 | |||||||
chr13:114182532 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.90+3112G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182532 | |||||||
chr13:114182538 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0085 a0001c0001t0001g0086 others(15): Show |
19 | HG00408.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.90+3118G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182538 | |||||||
chr13:114182539 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0086 a0001c0001t0001g0087 others(11): Show |
15 | HG00408.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3119T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182539 | |||||||
chr13:114182542 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3122T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182542 | |||||||
chr13:114182559 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3139G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182559 | |||||||
chr13:114182567 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3147C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182567 | |||||||
chr13:114182581 | C | A | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3161C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182581 | |||||||
chr13:114182582 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3162G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182582 | |||||||
chr13:114182584 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3164T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182584 | |||||||
chr13:114182605 | C | T | 13 | a0001c0001t0004g0035 a0001c0001t0004g0260 a0001c0001t0006g0013 others(10): Show |
17 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3185C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182605 | |||||||
chr13:114182613 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
272 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.90+3193T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182613 | |||||||
chr13:114182614 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3194G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182614 | |||||||
chr13:114182622 | T | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0316 a0001c0001t0010g0317 |
3 | HG01167.hp2 HG01169.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.90+3202T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182622 | |||||||
chr13:114182623 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3203T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182623 | |||||||
chr13:114182626 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.90+3206G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182626 | |||||||
chr13:114182672 | T | C | 4 | a0001c0001t0004g0047 a0001c0001t0004g0230 a0001c0001t0004g0243 others(1): Show |
4 | NA18990.hp1 NA19009.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+3252T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182672 | |||||||
chr13:114182688 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG01884.hp1 HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.90+3268G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182688 | |||||||
chr13:114182705 | C | T | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0331 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3285C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182705 | |||||||
chr13:114182719 | C | G | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0331 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3299C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182719 | |||||||
chr13:114182739 | T | C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+3319T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182739 | |||||||
chr13:114182752 | G | A | 28 | a0001c0001t0001g0064 a0001c0001t0001g0079 a0001c0001t0005g0018 others(25): Show |
31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.90+3332G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182752 | |||||||
chr13:114182760 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3340A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182760 | |||||||
chr13:114182783 | T | G | 1 | a0001c0001t0003g0157 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.90+3363T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182783 | |||||||
chr13:114182819 | T | C | 73 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(70): Show |
83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.90+3399T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182819 | |||||||
chr13:114182936 | A | G | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+3516A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182936 | |||||||
chr13:114182947 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.90+3527G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182947 | |||||||
chr13:114183048 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.90+3628G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183048 | |||||||
chr13:114183054 | T | C | 1 | a0001c0001t0003g0148 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.90+3634T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183054 | |||||||
chr13:114183099 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(104): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.90+3679C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183099 | |||||||
chr13:114183163 | A | ATTATTTA others(5): Show |
12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3754_90+3765dup others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114183163 | ||||||
chr13:114183198 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3778A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183198 | |||||||
chr13:114183311 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+3891C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183311 | |||||||
chr13:114183321 | C | T | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+3901C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183321 | |||||||
chr13:114183419 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0136 |
3 | HG02723.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.90+3999C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183419 | |||||||
chr13:114183420 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.90+4000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183420 | |||||||
chr13:114183460 | A | T | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.90+4040A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183460 | |||||||
chr13:114183463 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+4043C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183463 | |||||||
chr13:114183570 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0004g0234 a0001c0001t0004g0262 |
3 | HG01928.hp2 HG01952.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.90+4150G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183570 | |||||||
chr13:114183596 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+4176T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183596 | |||||||
chr13:114183621 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4201A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183621 | |||||||
chr13:114183675 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.90+4255G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183675 | |||||||
chr13:114183765 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG00735.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.90+4345G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183765 | |||||||
chr13:114183771 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90+4351C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183771 | |||||||
chr13:114183835 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+4415G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183835 | |||||||
chr13:114183839 | C | G | 77 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(74): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+4419C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183839 | |||||||
chr13:114183907 | G | C | 1 | a0001c0001t0002g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.90+4487G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183907 | |||||||
chr13:114183960 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4540C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183960 | |||||||
chr13:114184001 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4581G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184001 | |||||||
chr13:114184164 | G | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+4744G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184164 | |||||||
chr13:114184250 | T | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(92): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.90+4830T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184250 | |||||||
chr13:114184336 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4916T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184336 | |||||||
chr13:114184352 | G | A | 31 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0249 others(28): Show |
39 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+4932G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184352 | |||||||
chr13:114184552 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(43): Show |
51 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.90+5132G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184552 | |||||||
chr13:114184595 | G | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+5175G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184595 | |||||||
chr13:114184604 | G | A | 34 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(31): Show |
37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+5184G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184604 | |||||||
chr13:114184623 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.90+5203T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184623 | |||||||
chr13:114184638 | T | C | 34 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(31): Show |
37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+5218T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184638 | |||||||
chr13:114184682 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+5262T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184682 | |||||||
chr13:114184719 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+5299T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184719 | |||||||
chr13:114184800 | A | G | 1 | a0001c0001t0004g0259 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.90+5380A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184800 | |||||||
chr13:114184821 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+5401A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184821 | |||||||
chr13:114184959 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+5539T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184959 | |||||||
chr13:114185195 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90+5775C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185195 | |||||||
chr13:114185271 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0114 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.90+5851G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185271 | |||||||
chr13:114185292 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+5872C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185292 | |||||||
chr13:114185293 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+5873G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185293 | |||||||
chr13:114185518 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0326 |
2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.90+6098C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185518 | |||||||
chr13:114185583 | C | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(18): Show |
27 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+6163C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185583 | |||||||
chr13:114185597 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+6177G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185597 | |||||||
chr13:114185656 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+6236C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185656 | |||||||
chr13:114185832 | G | GC | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6413dupC | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114185832 | ||||||
chr13:114185854 | C | T | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.90+6434C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185854 | |||||||
chr13:114185895 | C | G | 1 | a0001c0001t0003g0024 | 2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.90+6475C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185895 | |||||||
chr13:114185964 | T | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6544T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185964 | |||||||
chr13:114185975 | T | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6555T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185975 | |||||||
chr13:114186066 | C | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6646C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186066 | |||||||
chr13:114186132 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.90+6712G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186132 | |||||||
chr13:114186143 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6723T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186143 | |||||||
chr13:114186229 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+6809G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186229 | |||||||
chr13:114186229 | G | T | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.90+6809G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186229 | |||||||
chr13:114186318 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6898T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186318 | |||||||
chr13:114186357 | C | T | 36 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(33): Show |
39 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.90+6937C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186357 | |||||||
chr13:114186420 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+7000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186420 | |||||||
chr13:114186441 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+7021C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186441 | |||||||
chr13:114186584 | T | G | 48 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(45): Show |
54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.90+7164T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186584 | |||||||
chr13:114186695 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.90+7275G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186695 | |||||||
chr13:114186705 | T | C | 34 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(31): Show |
37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+7285T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186705 | |||||||
chr13:114186842 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+7422C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186842 | |||||||
chr13:114186875 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.90+7455T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186875 | |||||||
chr13:114186893 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+7473C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186893 | |||||||
chr13:114186938 | C | T | 39 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(36): Show |
43 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.90+7518C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186938 | |||||||
chr13:114187098 | G | A | 77 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(74): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+7678G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187098 | |||||||
chr13:114187398 | A | G | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+7978A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187398 | |||||||
chr13:114187556 | G | C | 77 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(74): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+8136G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187556 | |||||||
chr13:114187556 | G | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+8136G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187556 | |||||||
chr13:114187645 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+8225A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187645 | |||||||
chr13:114187724 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0122 others(1): Show |
5 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+8304C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187724 | |||||||
chr13:114188081 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.91-8315C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188081 | |||||||
chr13:114188115 | CA | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(21): Show |
30 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.91-8268delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188115 | ||||||
chr13:114188158 | C | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.91-8238C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188158 | |||||||
chr13:114188271 | C | CA | 9 | a0001c0001t0001g0125 a0001c0001t0001g0141 a0001c0001t0001g0212 others(6): Show |
9 | HG01167.hp1 HG01243.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-8107dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | ||||||
chr13:114188271 | CA | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0029 others(43): Show |
53 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.91-8107delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | ||||||
chr13:114188271 | CAA | C | 86 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(83): Show |
99 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-8108_91-8107del others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | ||||||
chr13:114188516 | G | A | 51 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0224 others(48): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.91-7880G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188516 | |||||||
chr13:114188634 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.91-7762G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188634 | |||||||
chr13:114188689 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-7707A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188689 | |||||||
chr13:114188776 | C | CAA | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-7606_91-7605dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188776 | ||||||
chr13:114188776 | CA | C | 6 | a0001c0001t0001g0211 a0001c0001t0001g0227 a0001c0001t0002g0050 others(3): Show |
6 | HG01496.hp1 HG02976.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-7605delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188776 | ||||||
chr13:114188807 | A | G | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-7589A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188807 | |||||||
chr13:114189218 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-7178C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189218 | |||||||
chr13:114189250 | A | C | 1 | a0001c0001t0008g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.91-7146A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189250 | |||||||
chr13:114189436 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-6960C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189436 | |||||||
chr13:114189613 | T | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6783T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189613 | |||||||
chr13:114189635 | G | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0203 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.91-6761G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189635 | |||||||
chr13:114189682 | G | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-6714G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189682 | |||||||
chr13:114189709 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6687A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189709 | |||||||
chr13:114189726 | TCATATC | T | 52 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0224 others(49): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.91-6669_91-6664del others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189726 | |||||||
chr13:114189855 | T | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-6541T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189855 | |||||||
chr13:114189898 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0002g0297 |
2 | HG01081.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.91-6498T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189898 | |||||||
chr13:114189912 | A | C | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.91-6484A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189912 | |||||||
chr13:114189948 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91-6448C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189948 | |||||||
chr13:114189959 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(138): Show |
163 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.91-6437T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189959 | |||||||
chr13:114190001 | A | G | 48 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(45): Show |
54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.91-6395A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190001 | |||||||
chr13:114190004 | C | T | 77 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(74): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.91-6392C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190004 | |||||||
chr13:114190061 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.91-6335G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190061 | |||||||
chr13:114190106 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.91-6290C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190106 | |||||||
chr13:114190137 | G | A | 67 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0003g0006 others(64): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.91-6259G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190137 | |||||||
chr13:114190137 | G | C | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-6259G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190137 | |||||||
chr13:114190141 | TA | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(36): Show |
44 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.91-6245delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114190141 | ||||||
chr13:114190153 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6243G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190153 | |||||||
chr13:114190220 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.91-6176A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190220 | |||||||
chr13:114190262 | C | T | 48 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(45): Show |
54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.91-6134C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190262 | |||||||
chr13:114190271 | C | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG00140.hp1 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-6125C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190271 | |||||||
chr13:114190357 | G | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-6039G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190357 | |||||||
chr13:114190402 | C | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-5994C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190402 | |||||||
chr13:114190406 | TAATC | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(215): Show |
250 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.91-5986_91-5983del others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114190406 | ||||||
chr13:114190455 | A | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5941A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190455 | |||||||
chr13:114190679 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-5717T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190679 | |||||||
chr13:114190993 | A | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5403A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190993 | |||||||
chr13:114191080 | A | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5316A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191080 | |||||||
chr13:114191175 | G | T | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.91-5221G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191175 | |||||||
chr13:114191235 | C | G | 1 | a0001c0001t0012g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.91-5161C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191235 | |||||||
chr13:114191298 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(92): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.91-5098G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191298 | |||||||
chr13:114191346 | G | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5050G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191346 | |||||||
chr13:114191369 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91-5027C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191369 | |||||||
chr13:114191559 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.91-4837C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191559 | |||||||
chr13:114191827 | A | G | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4569A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191827 | |||||||
chr13:114191828 | G | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4568G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191828 | |||||||
chr13:114191829 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4567A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191829 | |||||||
chr13:114191855 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4541A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191855 | |||||||
chr13:114191856 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4540T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191856 | |||||||
chr13:114191857 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4539A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191857 | |||||||
chr13:114191858 | A | C | 2 | a0001c0002t0001g0201 a0001c0002t0001g0203 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.91-4538A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191858 | |||||||
chr13:114191895 | T | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-4501T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191895 | |||||||
chr13:114191910 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0297 |
2 | HG01081.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.91-4486G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191910 | |||||||
chr13:114192057 | C | T | 1 | a0001c0001t0002g0309 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.91-4339C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192057 | |||||||
chr13:114192082 | G | A | 8 | a0001c0001t0003g0148 a0001c0001t0003g0160 a0001c0001t0006g0013 others(5): Show |
10 | HG00642.hp2 HG01993.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.91-4314G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192082 | |||||||
chr13:114192148 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(6): Show |
12 | HG01070.hp1 HG01168.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-4248C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192148 | |||||||
chr13:114192182 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0138 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91-4214T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192182 | |||||||
chr13:114192213 | C | T | 46 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(43): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.91-4183C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192213 | |||||||
chr13:114192251 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.91-4145G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192251 | |||||||
chr13:114192262 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.91-4134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192262 | |||||||
chr13:114192404 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-3992T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192404 | |||||||
chr13:114192406 | T | A | 1 | a0001c0001t0003g0158 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.91-3990T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192406 | |||||||
chr13:114192435 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.91-3961C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192435 | |||||||
chr13:114192529 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0249 |
2 | NA18986.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.91-3867A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192529 | |||||||
chr13:114192636 | C | G | 1 | a0001c0001t0002g0038 | 2 | HG01192.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.91-3760C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192636 | |||||||
chr13:114192692 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91-3704G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192692 | |||||||
chr13:114192698 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.91-3698A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192698 | |||||||
chr13:114192708 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91-3688G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192708 | |||||||
chr13:114192806 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.91-3590T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192806 | |||||||
chr13:114192973 | A | G | 1 | a0001c0001t0005g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.91-3423A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192973 | |||||||
chr13:114193218 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.91-3178A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193218 | |||||||
chr13:114193219 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.91-3177T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193219 | |||||||
chr13:114193379 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-3017A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193379 | |||||||
chr13:114193401 | T | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-2995T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193401 | |||||||
chr13:114193405 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2991T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193405 | |||||||
chr13:114193736 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91-2660G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193736 | |||||||
chr13:114193768 | C | G | 1 | a0001c0001t0003g0150 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.91-2628C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193768 | |||||||
chr13:114193860 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0341 others(1): Show |
4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-2536G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193860 | |||||||
chr13:114193917 | C | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2479C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193917 | |||||||
chr13:114194033 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-2363G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194033 | |||||||
chr13:114194163 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2233T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194163 | |||||||
chr13:114194389 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0065 others(34): Show |
41 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.91-2007A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194389 | |||||||
chr13:114194424 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-1972G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194424 | |||||||
chr13:114194426 | A | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-1970A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194426 | |||||||
chr13:114194585 | C | T | 74 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(71): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.91-1811C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194585 | |||||||
chr13:114194688 | C | T | 13 | a0001c0001t0001g0125 a0001c0001t0006g0013 a0001c0001t0006g0040 others(10): Show |
16 | HG00642.hp2 HG01361.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.91-1708C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194688 | |||||||
chr13:114194702 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.91-1694C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194702 | |||||||
chr13:114194734 | C | CT | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.91-1662_91-1661ins others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194734 | |||||||
chr13:114194757 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.91-1639A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194757 | |||||||
chr13:114194803 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-1593A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194803 | |||||||
chr13:114194843 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(90): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.91-1553A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194843 | |||||||
chr13:114194956 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-1440C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194956 | |||||||
chr13:114195007 | T | C | 1 | a0001c0001t0005g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.91-1389T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195007 | |||||||
chr13:114195014 | A | C | 1 | a0001c0001t0006g0332 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.91-1382A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195014 | |||||||
chr13:114195051 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91-1345C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195051 | |||||||
chr13:114195087 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.91-1309T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195087 | |||||||
chr13:114195123 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0106 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.91-1273G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195123 | |||||||
chr13:114195207 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-1189G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195207 | |||||||
chr13:114195227 | G | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | NA18942.hp2 NA18962.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-1169G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195227 | |||||||
chr13:114195255 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.91-1141T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195255 | |||||||
chr13:114195337 | G | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-1059G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195337 | |||||||
chr13:114195555 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.91-841A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195555 | |||||||
chr13:114195864 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.91-532A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195864 | |||||||
chr13:114195916 | CA | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.91-463delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114195916 | ||||||
chr13:114195916 | CAA | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(118): Show |
136 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.91-464_91-463delAA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114195916 | ||||||
chr13:114195926 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.91-470A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195926 | |||||||
chr13:114195929 | A | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-467A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195929 | |||||||
chr13:114195931 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.91-465A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195931 | |||||||
chr13:114195956 | G | A | 1 | a0001c0001t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.91-440G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195956 | |||||||
chr13:114196008 | G | A | 129 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(126): Show |
149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.91-388G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196008 | |||||||
chr13:114196076 | C | CAAA | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-302_91-300dupAA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | ||||||
chr13:114196076 | CA | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0202 others(5): Show |
9 | HG00735.hp2 HG01071.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-300delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | ||||||
chr13:114196076 | CAA | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(58): Show |
71 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.91-301_91-300delAA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | ||||||
chr13:114196076 | CAAA | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(152): Show |
179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.91-302_91-300delAA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | ||||||
chr13:114196076 | CAAAA | C | 38 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(35): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.91-303_91-300delAA others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | ||||||
chr13:114196099 | C | T | 1 | a0001c0001t0003g0178 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.91-297C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196099 | |||||||
chr13:114196113 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-283G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196113 | |||||||
chr13:114196262 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG00735.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.91-134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196262 | |||||||
chr13:114196286 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91-110G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196286 | |||||||
chr13:114196642 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.171+166G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114196642 | |||||||
chr13:114197026 | G | A | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
10 | NA18954.hp2 NA18963.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+550G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197026 | |||||||
chr13:114197032 | T | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+556T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197032 | |||||||
chr13:114197143 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.171+667T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197143 | |||||||
chr13:114197280 | TA | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+805delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197280 | |||||||
chr13:114197281 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0220 a0001c0001t0001g0223 |
4 | HG02818.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+805A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197281 | |||||||
chr13:114197326 | C | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.171+850C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197326 | |||||||
chr13:114197478 | G | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1002G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197478 | |||||||
chr13:114197529 | G | A | 74 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(71): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.171+1053G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197529 | |||||||
chr13:114197565 | A | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1089A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197565 | |||||||
chr13:114197611 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1135G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197611 | |||||||
chr13:114197622 | GA | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1148delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114197622 | ||||||
chr13:114197735 | T | TCCAGTGA others(45): Show |
8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1260_171+1311d others(54): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114197735 | ||||||
chr13:114197846 | T | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1370T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197846 | |||||||
chr13:114197856 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1380C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197856 | |||||||
chr13:114197961 | A | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(65): Show |
78 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.171+1485A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197961 | |||||||
chr13:114198147 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.171+1671C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198147 | |||||||
chr13:114198162 | T | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0080 others(12): Show |
16 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+1686T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198162 | |||||||
chr13:114198282 | G | A | 67 | a0001c0001t0001g0120 a0001c0001t0003g0006 a0001c0001t0003g0007 others(64): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.171+1806G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198282 | |||||||
chr13:114198362 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(178): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.171+1886C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198362 | |||||||
chr13:114198366 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0135 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.171+1890C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198366 | |||||||
chr13:114198384 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1908A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198384 | |||||||
chr13:114198429 | A | G | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1896A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198429 | |||||||
chr13:114198507 | C | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1818C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198507 | |||||||
chr13:114198519 | C | G | 1 | a0001c0001t0003g0340 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.172-1806C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198519 | |||||||
chr13:114198534 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-1791C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198534 | |||||||
chr13:114198585 | C | G | 1 | a0001c0001t0003g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.172-1740C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198585 | |||||||
chr13:114198605 | G | C | 67 | a0001c0001t0001g0120 a0001c0001t0003g0006 a0001c0001t0003g0007 others(64): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-1720G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198605 | |||||||
chr13:114198619 | T | TGGTCCCC others(32): Show |
12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1692_172-1691i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | ||||||
chr13:114198619 | T | TGGTCCCC others(500): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0241 |
3 | HG01168.hp2 HG04228.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | ||||||
chr13:114198619 | T | TGGTCCCC others(461): Show |
13 | a0001c0001t0001g0046 a0001c0001t0001g0119 a0001c0001t0001g0224 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1671_172-1670i others(470): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | ||||||
chr13:114198619 | T | TGGTCCCC others(500): Show |
1 | a0001c0001t0001g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | ||||||
chr13:114198619 | TGGTCCCC others(71): Show |
T | 1 | a0001c0001t0002g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.172-1670_172-1593d others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | ||||||
chr13:114198623 | C | T | 74 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(71): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.172-1702C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198623 | |||||||
chr13:114198629 | TGAGGGGT others(266): Show |
T | 1 | a0001c0001t0001g0022 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.172-1670_172-1398d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198629 | ||||||
chr13:114198640 | GGCGCGTC others(188): Show |
G | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1670_172-1476d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198640 | ||||||
chr13:114198654 | T | TGTACGGT others(266): Show |
1 | a0001c0001t0004g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(384): Show |
1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(344): Show |
2 | a0001c0001t0001g0227 a0001c0001t0004g0260 |
2 | HG02976.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(383): Show |
5 | a0001c0001t0001g0265 a0001c0001t0004g0031 a0001c0001t0004g0238 others(2): Show |
6 | HG00140.hp1 HG02083.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1671_172-1670i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(969): Show |
1 | a0001c0001t0004g0009 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(978): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(969): Show |
1 | a0001c0001t0004g0009 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(978): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(851): Show |
1 | a0001c0001t0012g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(860): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(968): Show |
3 | a0001c0001t0004g0009 a0001c0001t0004g0244 a0001c0001t0004g0256 |
3 | NA18947.hp1 NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(977): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(1046): Show |
1 | a0001c0001t0004g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(1055): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(344): Show |
1 | a0001c0004t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(968): Show |
1 | a0001c0001t0004g0248 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(977): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(344): Show |
1 | a0001c0001t0004g0253 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | T | TGTACGGT others(188): Show |
1 | a0001c0001t0001g0207 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | TTTACGGT others(32): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172-1670_172-1632d others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198654 | TTTACGGT others(656): Show |
T | 1 | a0001c0001t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-1670_172-1008d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | |||||||
chr13:114198655 | T | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(162): Show |
192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.172-1670T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198655 | |||||||
chr13:114198657 | A | ACGGTCCC others(149): Show |
1 | a0001c0001t0002g0003 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198657 | ||||||
chr13:114198666 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(78): Show |
94 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.172-1659G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198666 | |||||||
chr13:114198666 | G | GCTGAGGG others(32): Show |
5 | a0001c0001t0001g0084 a0001c0001t0001g0127 a0001c0001t0001g0129 others(2): Show |
5 | HG01243.hp1 HG01258.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198666 | ||||||
chr13:114198666 | G | GCTGAGGG others(110): Show |
12 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0232 others(9): Show |
13 | HG00733.hp2 HG02129.hp2 HG03471.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198666 | ||||||
chr13:114198668 | T | TGAGGGGT others(151): Show |
1 | a0001c0001t0001g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-1653_172-1652i others(160): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(71): Show |
4 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
6 | HG00741.hp2 HG02155.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(149): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(8): Show |
14 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(227): Show |
8 | a0001c0001t0001g0263 a0001c0001t0004g0032 a0001c0001t0004g0035 others(5): Show |
10 | HG00673.hp1 HG02145.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(236): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(110): Show |
1 | a0001c0001t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.172-1653_172-1652i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(149): Show |
9 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0112 others(6): Show |
9 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(188): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0122 others(2): Show |
6 | HG02630.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | T | TGAGGGGT others(188): Show |
1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.172-1653_172-1652i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198668 | TGAGGCGT others(890): Show |
T | 1 | a0001c0001t0008g0090 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172-1646_172-750de others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | ||||||
chr13:114198671 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1654G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198671 | |||||||
chr13:114198673 | C | CGTGACGG others(383): Show |
1 | a0001c0001t0005g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | ||||||
chr13:114198673 | C | CGTGACGG others(344): Show |
1 | a0001c0001t0001g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | ||||||
chr13:114198673 | C | CGTGACGG others(383): Show |
24 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(21): Show |
26 | HG00408.hp1 HG01891.hp1 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | ||||||
chr13:114198673 | C | CGTGACGG others(344): Show |
1 | a0001c0001t0001g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | ||||||
chr13:114198673 | C | CGTGACGG others(383): Show |
1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | ||||||
chr13:114198673 | C | G | 40 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(37): Show |
44 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.172-1652C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198673 | |||||||
chr13:114198679 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
305 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.172-1646A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198679 | |||||||
chr13:114198681 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
310 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.172-1644T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198681 | |||||||
chr13:114198683 | G | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
310 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.172-1642G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198683 | |||||||
chr13:114198693 | C | CTTACGGT others(32): Show |
8 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
9 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1632_172-1631i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | |||||||
chr13:114198693 | C | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(142): Show |
171 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.172-1632C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | |||||||
chr13:114198693 | C | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0004g0009 others(5): Show |
10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1632C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | |||||||
chr13:114198694 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1631G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198694 | |||||||
chr13:114198694 | G | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0065 others(45): Show |
52 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.172-1631G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198694 | |||||||
chr13:114198698 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172-1627G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198698 | |||||||
chr13:114198705 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0138 others(6): Show |
11 | HG00741.hp2 HG01169.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-1620G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198705 | |||||||
chr13:114198707 | T | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(121): Show |
145 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.172-1618T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198707 | |||||||
chr13:114198712 | G | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(159): Show |
188 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.172-1613G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198712 | |||||||
chr13:114198718 | G | A | 3 | a0001c0001t0001g0242 a0001c0001t0004g0234 a0001c0001t0004g0262 |
3 | HG01169.hp1 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.172-1607G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198718 | |||||||
chr13:114198732 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.172-1593T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198732 | |||||||
chr13:114198732 | T | G | 124 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(121): Show |
143 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.172-1593T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198732 | |||||||
chr13:114198732 | T | TGTACGGT others(305): Show |
1 | a0001c0001t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.172-1589_172-1588i others(314): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198732 | ||||||
chr13:114198733 | G | GTACGGTC others(149): Show |
21 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0066 others(18): Show |
22 | HG02602.hp1 HG02698.hp2 HG03486.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-1589_172-1588i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | ||||||
chr13:114198733 | G | GTACGGTC others(188): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0213 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.172-1589_172-1588i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | ||||||
chr13:114198733 | G | GTACGGTC others(227): Show |
1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.172-1589_172-1588i others(236): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | ||||||
chr13:114198733 | G | GTACGGTC others(500): Show |
1 | a0001c0001t0005g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.172-1589_172-1588i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | ||||||
chr13:114198733 | G | GTACGGTC others(149): Show |
8 | a0001c0001t0001g0079 a0001c0001t0001g0212 a0001c0001t0001g0215 others(5): Show |
8 | HG00408.hp2 HG00621.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-1589_172-1588i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | ||||||
chr13:114198733 | G | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
34 | HG00609.hp2 HG00673.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.172-1592G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198733 | |||||||
chr13:114198737 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
312 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.172-1588A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198737 | |||||||
chr13:114198744 | G | A | 10 | a0001c0001t0001g0084 a0001c0001t0001g0127 a0001c0001t0001g0128 others(7): Show |
10 | HG00558.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1581G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198744 | |||||||
chr13:114198746 | T | C | 104 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(101): Show |
120 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.172-1579T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198746 | |||||||
chr13:114198749 | G | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0244 a0001c0001t0004g0248 others(1): Show |
6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1576G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198749 | |||||||
chr13:114198751 | G | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(133): Show |
159 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-1574G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198751 | |||||||
chr13:114198757 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172-1568G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198757 | |||||||
chr13:114198771 | C | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(106): Show |
125 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.172-1554C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198771 | |||||||
chr13:114198771 | C | T | 18 | a0001c0001t0001g0316 a0001c0001t0002g0310 a0001c0001t0004g0253 others(15): Show |
21 | HG00544.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-1554C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198771 | |||||||
chr13:114198772 | T | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(148): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.172-1553T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198772 | |||||||
chr13:114198782 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.172-1543T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198782 | |||||||
chr13:114198783 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(91): Show |
110 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.172-1542G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198783 | |||||||
chr13:114198785 | T | C | 26 | a0001c0001t0001g0084 a0001c0001t0001g0114 a0001c0001t0001g0120 others(23): Show |
29 | HG00733.hp2 HG00741.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-1540T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198785 | |||||||
chr13:114198788 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1537G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198788 | |||||||
chr13:114198790 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(74): Show |
91 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.172-1535C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198790 | |||||||
chr13:114198790 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1535C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198790 | |||||||
chr13:114198796 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.172-1529A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198796 | |||||||
chr13:114198798 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.172-1527T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198798 | |||||||
chr13:114198800 | G | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.172-1525G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198800 | |||||||
chr13:114198801 | G | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(68): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.172-1524G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198801 | |||||||
chr13:114198806 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-1519C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198806 | |||||||
chr13:114198808 | T | TGCTTACG others(186): Show |
1 | a0001c0001t0001g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.172-1516_172-1515i others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198808 | ||||||
chr13:114198810 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(142): Show |
164 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.172-1515T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198810 | |||||||
chr13:114198810 | T | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(104): Show |
123 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.172-1515T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198810 | |||||||
chr13:114198810 | T | TGTACGGT others(110): Show |
2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.172-1502_172-1501i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198810 | ||||||
chr13:114198811 | G | GTACGGTC others(344): Show |
1 | a0001c0001t0005g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.172-1497_172-1496i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198811 | ||||||
chr13:114198811 | G | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0029 others(78): Show |
89 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.172-1514G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198811 | |||||||
chr13:114198817 | T | TCCCCGCT others(73): Show |
1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172-1497_172-1496i others(82): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198817 | ||||||
chr13:114198822 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0192 a0001c0001t0002g0310 others(1): Show |
4 | HG00558.hp2 HG01123.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1503G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198822 | |||||||
chr13:114198824 | T | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(87): Show |
105 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-1501T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198824 | |||||||
chr13:114198829 | C | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0059 others(66): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.172-1496C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198829 | |||||||
chr13:114198835 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
312 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.172-1490A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198835 | |||||||
chr13:114198840 | G | T | 1 | a0001c0001t0003g0153 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.172-1485G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198840 | |||||||
chr13:114198847 | T | TGCTTACG others(264): Show |
1 | a0001c0001t0012g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.172-1477_172-1476i others(273): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | ||||||
chr13:114198847 | T | TGCTTACG others(420): Show |
1 | a0001c0001t0005g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.172-1477_172-1476i others(429): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | ||||||
chr13:114198847 | T | TGCTTACG others(537): Show |
1 | a0001c0001t0005g0098 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.172-1477_172-1476i others(546): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | ||||||
chr13:114198849 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0029 others(142): Show |
159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-1476T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198849 | |||||||
chr13:114198849 | T | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(107): Show |
133 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.172-1476T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198849 | |||||||
chr13:114198850 | G | GCT | 3 | a0001c0001t0005g0092 a0001c0001t0005g0098 a0001c0001t0012g0320 |
3 | HG00423.hp2 HG01257.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.172-1475_172-1474i others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198850 | |||||||
chr13:114198850 | G | T | 108 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0041 others(105): Show |
119 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.172-1475G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198850 | |||||||
chr13:114198853 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172-1472C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198853 | |||||||
chr13:114198861 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(85): Show |
104 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.172-1464G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198861 | |||||||
chr13:114198863 | T | C | 13 | a0001c0001t0001g0120 a0001c0001t0001g0128 a0001c0001t0001g0192 others(10): Show |
13 | HG00558.hp2 HG01123.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1462T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198863 | |||||||
chr13:114198866 | G | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0244 a0001c0001t0004g0248 others(1): Show |
6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1459G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198866 | |||||||
chr13:114198868 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(117): Show |
142 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.172-1457G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198868 | |||||||
chr13:114198888 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.172-1437T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198888 | |||||||
chr13:114198888 | T | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(100): Show |
117 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.172-1437T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198888 | |||||||
chr13:114198889 | G | GTACGGTC others(384): Show |
1 | a0001c0001t0007g0156 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.172-1426_172-1425i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | ||||||
chr13:114198889 | G | GTACGGTC others(384): Show |
1 | a0001c0001t0008g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.172-1426_172-1425i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | ||||||
chr13:114198889 | G | GTACGGTC others(266): Show |
1 | a0001c0001t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.172-1426_172-1425i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | ||||||
chr13:114198889 | G | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0034 others(79): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.172-1436G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198889 | |||||||
chr13:114198900 | A | ACTGAGGC others(32): Show |
1 | a0001c0001t0006g0338 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.172-1424_172-1423i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198900 | ||||||
chr13:114198900 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
298 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.172-1425A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198900 | |||||||
chr13:114198902 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
216 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.172-1423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198902 | |||||||
chr13:114198907 | G | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0030 others(112): Show |
133 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.172-1418G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198907 | |||||||
chr13:114198916 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1409G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198916 | |||||||
chr13:114198917 | C | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1408C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198917 | |||||||
chr13:114198923 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1402C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198923 | |||||||
chr13:114198927 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(156): Show |
182 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.172-1398T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198927 | |||||||
chr13:114198927 | T | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(81): Show |
97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.172-1398T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198927 | |||||||
chr13:114198928 | G | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(50): Show |
60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.172-1397G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198928 | |||||||
chr13:114198939 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(66): Show |
80 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.172-1386G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198939 | |||||||
chr13:114198941 | T | C | 17 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0001g0242 others(14): Show |
19 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.172-1384T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198941 | |||||||
chr13:114198944 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1381G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198944 | |||||||
chr13:114198946 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
171 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.172-1379T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198946 | |||||||
chr13:114198946 | T | G | 129 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0029 others(126): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.172-1379T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198946 | |||||||
chr13:114198951 | T | C | 339 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
396 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(393): Show |
intron_variant | MODIFIER | c.172-1374T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198951 | |||||||
chr13:114198966 | G | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(149): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.172-1359G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198966 | |||||||
chr13:114198966 | G | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
101 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.172-1359G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198966 | |||||||
chr13:114198967 | G | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(54): Show |
63 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.172-1358G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198967 | |||||||
chr13:114198978 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
302 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.172-1347A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198978 | |||||||
chr13:114198980 | T | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(72): Show |
86 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.172-1345T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198980 | |||||||
chr13:114198980 | T | TGAGGCGT others(32): Show |
1 | a0001c0001t0002g0310 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1335_172-1334i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198980 | ||||||
chr13:114198985 | C | G | 131 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(128): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.172-1340C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198985 | |||||||
chr13:114198991 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.172-1334A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198991 | |||||||
chr13:114198993 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1332C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198993 | |||||||
chr13:114198994 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1331G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198994 | |||||||
chr13:114198995 | C | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1330C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198995 | |||||||
chr13:114198995 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1330C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198995 | |||||||
chr13:114198996 | G | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1329G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198996 | |||||||
chr13:114199001 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1324C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199001 | |||||||
chr13:114199003 | T | TGCTTACG others(30): Show |
11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1321_172-1320i others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | ||||||
chr13:114199003 | T | TGCTTACG others(537): Show |
1 | a0001c0001t0007g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.172-1321_172-1320i others(546): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | ||||||
chr13:114199003 | T | TGCTTACG others(225): Show |
1 | a0001c0001t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-1321_172-1320i others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | ||||||
chr13:114199005 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.172-1320T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | |||||||
chr13:114199005 | T | CTTACGGT others(32): Show |
1 | a0001c0001t0006g0338 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.172-1321_172-1320i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | |||||||
chr13:114199005 | T | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0022 others(75): Show |
92 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.172-1320T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | |||||||
chr13:114199006 | G | GCTTACGG others(34): Show |
11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1319_172-1318i others(43): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199006 | |||||||
chr13:114199006 | G | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0064 others(76): Show |
88 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.172-1319G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199006 | |||||||
chr13:114199008 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1317A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199008 | |||||||
chr13:114199009 | C | T | 38 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0025 others(35): Show |
42 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.172-1316C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199009 | |||||||
chr13:114199019 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.172-1306C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199019 | |||||||
chr13:114199022 | G | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0244 a0001c0001t0004g0248 others(1): Show |
6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1303G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199022 | |||||||
chr13:114199024 | G | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0022 others(87): Show |
104 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.172-1301G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199024 | |||||||
chr13:114199034 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1291C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199034 | |||||||
chr13:114199044 | G | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(147): Show |
170 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.172-1281G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199044 | |||||||
chr13:114199044 | G | T | 39 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(36): Show |
46 | HG00408.hp1 HG00639.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-1281G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199044 | |||||||
chr13:114199045 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1280G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199045 | |||||||
chr13:114199045 | G | T | 65 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(62): Show |
68 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.172-1280G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199045 | |||||||
chr13:114199048 | C | T | 7 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0149 others(4): Show |
9 | HG00544.hp1 HG02135.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1277C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199048 | |||||||
chr13:114199056 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0002g0310 a0001c0001t0003g0175 |
4 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1269G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199056 | |||||||
chr13:114199058 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
99 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.172-1267T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199058 | |||||||
chr13:114199063 | C | CGTGACGG others(188): Show |
1 | a0001c0001t0001g0263 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-1243_172-1242i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199063 | ||||||
chr13:114199063 | C | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0029 others(112): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.172-1262C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199063 | |||||||
chr13:114199071 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172-1254C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199071 | |||||||
chr13:114199074 | G | T | 1 | a0001c0001t0002g0310 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1251G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199074 | |||||||
chr13:114199083 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(150): Show |
177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.172-1242T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199083 | |||||||
chr13:114199083 | T | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0022 others(87): Show |
105 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-1242T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199083 | |||||||
chr13:114199084 | G | GTACGGTC others(188): Show |
7 | a0001c0001t0004g0032 a0001c0001t0004g0035 a0001c0001t0004g0252 others(4): Show |
9 | HG00673.hp1 HG03490.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-1224_172-1223i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199084 | ||||||
chr13:114199084 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(47): Show |
56 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-1241G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199084 | |||||||
chr13:114199095 | G | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0271 a0001c0001t0003g0176 |
4 | HG00323.hp2 HG01074.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1230G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199095 | |||||||
chr13:114199097 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0022 others(81): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.172-1228T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199097 | |||||||
chr13:114199102 | C | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.172-1223C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199102 | |||||||
chr13:114199113 | G | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0271 |
3 | HG00323.hp2 HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-1212G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199113 | |||||||
chr13:114199122 | G | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.172-1203G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199122 | |||||||
chr13:114199122 | G | T | 40 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0089 others(37): Show |
46 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-1203G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199122 | |||||||
chr13:114199122 | GGTACGGT others(71): Show |
G | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.172-1191_172-1114d others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199122 | ||||||
chr13:114199123 | G | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(32): Show |
47 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.172-1202G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199123 | |||||||
chr13:114199134 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
299 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.172-1191A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199134 | |||||||
chr13:114199136 | T | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0022 others(41): Show |
54 | HG00323.hp2 HG00544.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.172-1189T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199136 | |||||||
chr13:114199136 | T | TGAGGCGT others(32): Show |
1 | a0001c0001t0002g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.172-1125_172-1087d others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199136 | ||||||
chr13:114199141 | C | CGTGACGG others(110): Show |
2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-1165_172-1164i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199141 | ||||||
chr13:114199141 | C | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(163): Show |
187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.172-1184C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199141 | |||||||
chr13:114199152 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.172-1173G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199152 | |||||||
chr13:114199159 | T | TGCTTACG others(69): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0222 |
5 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1165_172-1164i others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199159 | ||||||
chr13:114199161 | T | C | 123 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(120): Show |
137 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-1164T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199161 | |||||||
chr13:114199161 | T | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
99 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.172-1164T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199161 | |||||||
chr13:114199162 | G | GCT | 2 | a0001c0001t0001g0002 a0001c0001t0001g0222 |
5 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1163_172-1162i others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199162 | |||||||
chr13:114199162 | G | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0029 others(77): Show |
85 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.172-1163G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199162 | |||||||
chr13:114199173 | G | A | 1 | a0001c0001t0002g0037 | 2 | HG00323.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-1152G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199173 | |||||||
chr13:114199175 | C | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
232 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.172-1150C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199175 | |||||||
chr13:114199180 | C | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
99 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.172-1145C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199180 | |||||||
chr13:114199186 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-1139G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199186 | |||||||
chr13:114199200 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(117): Show |
141 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.172-1125T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199200 | |||||||
chr13:114199200 | T | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(117): Show |
137 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-1125T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199200 | |||||||
chr13:114199201 | G | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0200 a0001c0001t0001g0213 others(19): Show |
28 | HG00609.hp2 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.172-1124G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199201 | |||||||
chr13:114199204 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1121C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199204 | |||||||
chr13:114199212 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0002g0299 a0001c0001t0003g0162 others(1): Show |
4 | HG03225.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1113G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199212 | |||||||
chr13:114199214 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.172-1111C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199214 | |||||||
chr13:114199219 | C | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(138): Show |
161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.172-1106C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199219 | |||||||
chr13:114199225 | G | A | 2 | a0001c0001t0003g0163 a0001c0001t0003g0176 |
2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1100G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199225 | |||||||
chr13:114199227 | C | T | 2 | a0001c0001t0003g0163 a0001c0001t0003g0176 |
2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1098C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199227 | |||||||
chr13:114199229 | C | G | 2 | a0001c0001t0003g0163 a0001c0001t0003g0176 |
2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1096C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199229 | |||||||
chr13:114199230 | G | T | 1 | a0001c0001t0002g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.172-1095G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199230 | |||||||
chr13:114199235 | C | CGTGCTTA others(32): Show |
2 | a0001c0001t0001g0192 a0001c0001t0003g0179 |
2 | HG02080.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-1087_172-1086i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199235 | ||||||
chr13:114199235 | C | CGTGCTTA others(266): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1087_172-1086i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199235 | ||||||
chr13:114199235 | C | T | 2 | a0001c0001t0003g0163 a0001c0001t0003g0176 |
2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1090C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199235 | |||||||
chr13:114199239 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(131): Show |
156 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-1086G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199239 | |||||||
chr13:114199239 | G | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(65): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.172-1086G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199239 | |||||||
chr13:114199240 | G | A | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1085G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199240 | |||||||
chr13:114199240 | G | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.172-1085G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199240 | |||||||
chr13:114199242 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1083A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199242 | |||||||
chr13:114199251 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
256 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.172-1074A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199251 | |||||||
chr13:114199253 | T | C | 18 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0316 others(15): Show |
21 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.172-1072T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199253 | |||||||
chr13:114199256 | G | A | 18 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(15): Show |
19 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-1069G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199256 | |||||||
chr13:114199258 | C | G | 148 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(145): Show |
169 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.172-1067C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199258 | |||||||
chr13:114199264 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1061G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199264 | |||||||
chr13:114199266 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-1059C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199266 | |||||||
chr13:114199268 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0003g0163 a0001c0001t0003g0176 others(1): Show |
4 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1057C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199268 | |||||||
chr13:114199269 | T | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
319 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.172-1056T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199269 | |||||||
chr13:114199278 | G | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
143 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.172-1047G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199278 | |||||||
chr13:114199278 | G | T | 131 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(128): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.172-1047G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199278 | |||||||
chr13:114199279 | G | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(38): Show |
55 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-1046G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199279 | |||||||
chr13:114199290 | G | A | 11 | a0001c0001t0001g0086 a0001c0001t0002g0037 a0001c0001t0002g0299 others(8): Show |
14 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1035G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199290 | |||||||
chr13:114199292 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
305 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.172-1033C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199292 | |||||||
chr13:114199295 | G | A | 11 | a0001c0001t0001g0227 a0001c0001t0004g0031 a0001c0001t0004g0032 others(8): Show |
14 | HG00673.hp1 HG02083.hp2 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1030G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199295 | |||||||
chr13:114199297 | C | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.172-1028C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199297 | |||||||
chr13:114199303 | G | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1022G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199303 | |||||||
chr13:114199305 | C | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0213 a0001c0001t0001g0269 others(1): Show |
4 | HG01243.hp2 HG02280.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1020C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199305 | |||||||
chr13:114199307 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0003g0163 a0001c0001t0003g0176 others(1): Show |
4 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1018C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199307 | |||||||
chr13:114199308 | G | T | 2 | a0001c0001t0002g0037 a0001c0001t0007g0048 |
3 | HG00323.hp2 HG02148.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-1017G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199308 | |||||||
chr13:114199313 | C | CGTGCTTA others(32): Show |
2 | a0001c0001t0003g0162 a0001c0001t0003g0164 |
2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.172-1009_172-1008i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199313 | ||||||
chr13:114199313 | C | CGTGCTTA others(266): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0055 |
4 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1009_172-1008i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199313 | ||||||
chr13:114199317 | G | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.172-1008G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199317 | |||||||
chr13:114199317 | G | T | 110 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.172-1008G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199317 | |||||||
chr13:114199318 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0034 others(48): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.172-1007G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199318 | |||||||
chr13:114199320 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0055 others(2): Show |
6 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1005A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199320 | |||||||
chr13:114199329 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
319 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.172-996A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199329 | |||||||
chr13:114199331 | T | C | 64 | a0001c0001t0001g0054 a0001c0001t0001g0085 a0001c0001t0001g0087 others(61): Show |
73 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-994T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199331 | |||||||
chr13:114199334 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0004g0247 |
2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-991G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199334 | |||||||
chr13:114199336 | C | CGTGACGG others(501): Show |
1 | a0001c0001t0001g0242 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.172-970_172-969ins others(508): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199336 | ||||||
chr13:114199336 | C | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(145): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.172-989C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199336 | |||||||
chr13:114199342 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0120 a0001c0001t0001g0192 others(3): Show |
6 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-983G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199342 | |||||||
chr13:114199344 | C | G | 41 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0041 others(38): Show |
43 | HG00408.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.172-981C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199344 | |||||||
chr13:114199344 | C | T | 5 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0163 others(2): Show |
5 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-981C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199344 | |||||||
chr13:114199346 | C | CGTCCCCG others(71): Show |
2 | a0001c0001t0003g0168 a0001c0001t0003g0169 |
2 | NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.172-970_172-969ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199346 | ||||||
chr13:114199346 | C | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0163 others(2): Show |
5 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-979C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199346 | |||||||
chr13:114199346 | C | T | 2 | a0001c0001t0003g0162 a0001c0001t0003g0164 |
2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.172-979C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199346 | |||||||
chr13:114199352 | C | CGTGCTTA others(151): Show |
1 | a0001c0001t0003g0171 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.172-970_172-969ins others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | ||||||
chr13:114199352 | C | CGTGCTTA others(150): Show |
1 | a0001c0001t0003g0186 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.172-970_172-969ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | ||||||
chr13:114199352 | C | CGTGCTTA others(149): Show |
47 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(44): Show |
55 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-970_172-969ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | ||||||
chr13:114199352 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-973C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199352 | |||||||
chr13:114199356 | G | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(92): Show |
110 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.172-969G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199356 | |||||||
chr13:114199356 | G | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(120): Show |
145 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.172-969G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199356 | |||||||
chr13:114199357 | G | A | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-968G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199357 | |||||||
chr13:114199357 | G | GTACGGTC others(461): Show |
2 | a0001c0001t0004g0234 a0001c0001t0004g0262 |
2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.172-956_172-955ins others(468): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199357 | ||||||
chr13:114199357 | G | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(20): Show |
28 | HG00544.hp2 HG00673.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.172-968G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199357 | |||||||
chr13:114199359 | A | T | 54 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0006 others(51): Show |
62 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.172-966A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199359 | |||||||
chr13:114199368 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0271 |
3 | HG00323.hp2 HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-957G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199368 | |||||||
chr13:114199368 | G | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
8 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-957G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199368 | |||||||
chr13:114199370 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
303 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.172-955C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199370 | |||||||
chr13:114199373 | G | A | 2 | a0001c0001t0004g0253 a0001c0001t0004g0260 |
2 | HG00544.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.172-952G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199373 | |||||||
chr13:114199375 | C | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(153): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.172-950C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199375 | |||||||
chr13:114199381 | G | A | 62 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(59): Show |
70 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-944G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199381 | |||||||
chr13:114199383 | C | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-942C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199383 | |||||||
chr13:114199383 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-942C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199383 | |||||||
chr13:114199385 | C | CGTCCCCG others(188): Show |
8 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(5): Show |
10 | HG00544.hp1 HG00558.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-931_172-930ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199385 | ||||||
chr13:114199385 | C | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-940C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199385 | |||||||
chr13:114199385 | C | T | 58 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0006 others(55): Show |
66 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.172-940C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199385 | |||||||
chr13:114199386 | G | T | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.172-939G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199386 | |||||||
chr13:114199391 | C | CGTGCTTA others(32): Show |
1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172-931_172-930ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199391 | ||||||
chr13:114199391 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-934C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199391 | |||||||
chr13:114199395 | G | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
148 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-930G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199395 | |||||||
chr13:114199395 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0052 others(66): Show |
79 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.172-930G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199395 | |||||||
chr13:114199396 | G | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(38): Show |
50 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.172-929G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199396 | |||||||
chr13:114199398 | A | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-927A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199398 | |||||||
chr13:114199401 | G | T | 1 | a0001c0001t0002g0295 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-924G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199401 | |||||||
chr13:114199408 | CCGAGGCG others(539): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-916_172-371del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199408 | |||||||
chr13:114199409 | C | CGAGGCGT others(305): Show |
1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.172-892_172-891ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199409 | ||||||
chr13:114199409 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.172-916C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199409 | |||||||
chr13:114199412 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.172-913G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199412 | |||||||
chr13:114199414 | C | G | 122 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(119): Show |
136 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.172-911C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199414 | |||||||
chr13:114199420 | G | A | 4 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-905G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199420 | |||||||
chr13:114199422 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0074 others(32): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.172-903C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199422 | |||||||
chr13:114199422 | C | T | 4 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-903C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199422 | |||||||
chr13:114199424 | C | G | 4 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-901C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199424 | |||||||
chr13:114199424 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-901C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199424 | |||||||
chr13:114199425 | G | GTCCCCGT others(71): Show |
1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.172-880_172-879ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199425 | ||||||
chr13:114199430 | C | CGTGCTTA others(149): Show |
1 | a0001c0001t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.172-892_172-891ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199430 | ||||||
chr13:114199430 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(8): Show |
14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.172-895C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199430 | |||||||
chr13:114199434 | G | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(144): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.172-891G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199434 | |||||||
chr13:114199434 | G | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(82): Show |
96 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.172-891G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199434 | |||||||
chr13:114199435 | G | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(99): Show |
122 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.172-890G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199435 | |||||||
chr13:114199437 | A | T | 5 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(2): Show |
5 | NA18955.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-888A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199437 | |||||||
chr13:114199446 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
302 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.172-879A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199446 | |||||||
chr13:114199448 | T | C | 3 | a0001c0001t0001g0316 a0001c0001t0002g0310 a0001c0001t0010g0317 |
3 | HG00558.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-877T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199448 | |||||||
chr13:114199453 | C | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
207 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.172-872C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199453 | |||||||
chr13:114199459 | G | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(74): Show |
89 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-866G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199459 | |||||||
chr13:114199461 | C | G | 21 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0089 others(18): Show |
22 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-864C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199461 | |||||||
chr13:114199461 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(63): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-864C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199461 | |||||||
chr13:114199463 | C | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(63): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-862C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199463 | |||||||
chr13:114199463 | C | T | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(8): Show |
11 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-862C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199463 | |||||||
chr13:114199464 | T | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
320 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.172-861T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199464 | |||||||
chr13:114199469 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(63): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-856C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199469 | |||||||
chr13:114199473 | G | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
68 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.172-852G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199473 | |||||||
chr13:114199473 | G | T | 135 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0034 others(132): Show |
155 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.172-852G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199473 | |||||||
chr13:114199474 | G | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(16): Show |
25 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.172-851G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199474 | |||||||
chr13:114199476 | A | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(63): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-849A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199476 | |||||||
chr13:114199487 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(259): Show |
301 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.172-838C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199487 | |||||||
chr13:114199490 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(14): Show |
23 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.172-835G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199490 | |||||||
chr13:114199492 | C | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(110): Show |
127 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.172-833C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199492 | |||||||
chr13:114199498 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-827G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199498 | |||||||
chr13:114199500 | C | G | 14 | a0001c0001t0001g0227 a0001c0001t0004g0031 a0001c0001t0004g0032 others(11): Show |
17 | HG00673.hp1 HG01928.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.172-825C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199500 | |||||||
chr13:114199500 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-825C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199500 | |||||||
chr13:114199502 | C | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-823C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199502 | |||||||
chr13:114199508 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0054 others(7): Show |
11 | HG01496.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-817C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199508 | |||||||
chr13:114199512 | G | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(130): Show |
158 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.172-813G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199512 | |||||||
chr13:114199512 | G | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0034 others(59): Show |
74 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.172-813G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199512 | |||||||
chr13:114199513 | G | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(49): Show |
60 | HG00323.hp2 HG00733.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.172-812G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199513 | |||||||
chr13:114199515 | A | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-810A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199515 | |||||||
chr13:114199524 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
319 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.172-801A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199524 | |||||||
chr13:114199526 | T | C | 4 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0003g0175 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-799T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199526 | |||||||
chr13:114199529 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0080 others(11): Show |
15 | HG01258.hp2 HG01516.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-796G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199529 | |||||||
chr13:114199531 | C | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(210): Show |
242 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.172-794C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199531 | |||||||
chr13:114199537 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(15): Show |
21 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-788G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199537 | |||||||
chr13:114199539 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0004g0247 |
2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-786C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199539 | |||||||
chr13:114199539 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-786C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199539 | |||||||
chr13:114199541 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-784C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199541 | |||||||
chr13:114199541 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-784C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199541 | |||||||
chr13:114199547 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-778C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199547 | |||||||
chr13:114199551 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(97): Show |
120 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.172-774T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199551 | |||||||
chr13:114199551 | T | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0074 others(43): Show |
52 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.172-774T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199551 | |||||||
chr13:114199552 | G | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(121): Show |
143 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.172-773G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199552 | |||||||
chr13:114199554 | A | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-771A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199554 | |||||||
chr13:114199563 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-762G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199563 | |||||||
chr13:114199563 | G | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-762G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199563 | |||||||
chr13:114199565 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
305 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.172-760C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199565 | |||||||
chr13:114199570 | C | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(149): Show |
175 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.172-755C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199570 | |||||||
chr13:114199576 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-749G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199576 | |||||||
chr13:114199578 | C | G | 26 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-747C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199578 | |||||||
chr13:114199578 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-747C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199578 | |||||||
chr13:114199580 | C | G | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-745C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199580 | |||||||
chr13:114199586 | C | T | 61 | a0001c0001t0001g0054 a0001c0001t0001g0192 a0001c0001t0003g0006 others(58): Show |
71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-739C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199586 | |||||||
chr13:114199590 | C | CT | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-733dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199590 | ||||||
chr13:114199590 | C | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0222 others(3): Show |
9 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-735C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199590 | |||||||
chr13:114199590 | C | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0001g0074 others(58): Show |
71 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.172-735C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199590 | |||||||
chr13:114199591 | T | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.172-734T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199591 | |||||||
chr13:114199593 | A | ACGGTCCC others(32): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0055 |
4 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-717_172-716ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199593 | ||||||
chr13:114199593 | A | ACGGTCCC others(110): Show |
1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.172-717_172-716ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199593 | ||||||
chr13:114199593 | A | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-732A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199593 | |||||||
chr13:114199604 | T | C | 5 | a0001c0001t0001g0316 a0001c0001t0002g0277 a0001c0001t0002g0288 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-721T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199604 | |||||||
chr13:114199607 | G | A | 19 | a0001c0001t0001g0114 a0001c0001t0001g0127 a0001c0001t0001g0128 others(16): Show |
22 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.172-718G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199607 | |||||||
chr13:114199609 | C | CGTGACGG others(71): Show |
2 | a0001c0001t0002g0286 a0001c0001t0002g0321 |
2 | HG00673.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.172-683_172-682ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199609 | ||||||
chr13:114199609 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.172-716C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199609 | |||||||
chr13:114199615 | G | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03225.hp1 HG03491.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-710G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199615 | |||||||
chr13:114199617 | C | G | 15 | a0001c0001t0001g0227 a0001c0001t0004g0031 a0001c0001t0004g0032 others(12): Show |
18 | HG00673.hp1 HG01928.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.172-708C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199617 | |||||||
chr13:114199617 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-708C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199617 | |||||||
chr13:114199619 | C | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-706C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199619 | |||||||
chr13:114199619 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-706C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199619 | |||||||
chr13:114199625 | C | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-700C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199625 | |||||||
chr13:114199629 | C | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0010g0317 |
3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172-696C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199629 | |||||||
chr13:114199629 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0034 others(58): Show |
70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-696C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199629 | |||||||
chr13:114199630 | G | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0074 others(50): Show |
62 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.172-695G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199630 | |||||||
chr13:114199632 | A | T | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-693A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199632 | |||||||
chr13:114199643 | C | CGAGGCGT others(149): Show |
1 | a0001c0001t0002g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.172-657_172-656ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199643 | ||||||
chr13:114199643 | C | CGAGGCGT others(188): Show |
1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.172-658_172-657ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199643 | ||||||
chr13:114199643 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.172-682C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199643 | |||||||
chr13:114199645 | A | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
9 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-680A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199645 | |||||||
chr13:114199647 | G | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-678G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199647 | |||||||
chr13:114199648 | C | CGTGACAG others(71): Show |
6 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0333 others(3): Show |
9 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-672_172-671ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199648 | ||||||
chr13:114199648 | C | CGTGACAG others(149): Show |
5 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0337 others(2): Show |
5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-672_172-671ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199648 | ||||||
chr13:114199648 | C | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(179): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.172-677C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199648 | |||||||
chr13:114199649 | G | A | 1 | a0001c0001t0008g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.172-676G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199649 | |||||||
chr13:114199654 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-671G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199654 | |||||||
chr13:114199656 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0004g0247 |
2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-669C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199656 | |||||||
chr13:114199658 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-667C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199658 | |||||||
chr13:114199660 | T | TCCCCGTG others(151): Show |
1 | a0001c0001t0002g0297 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.172-657_172-656ins others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199660 | ||||||
chr13:114199664 | C | T | 6 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(3): Show |
6 | HG04115.hp2 NA18955.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-661C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199664 | |||||||
chr13:114199668 | C | G | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-657C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199668 | |||||||
chr13:114199668 | C | T | 18 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(15): Show |
20 | HG00544.hp2 HG00609.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.172-657C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199668 | |||||||
chr13:114199669 | T | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(222): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.172-656T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199669 | |||||||
chr13:114199669 | T | TTACGGTC others(149): Show |
1 | a0001c0001t0002g0289 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.172-644_172-643ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199669 | T | TTACGGTC others(110): Show |
1 | a0001c0001t0002g0319 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172-561_172-560ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199669 | T | TTACGGTC others(110): Show |
1 | a0001c0001t0002g0306 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199669 | T | TTACGGTC others(150): Show |
1 | a0001c0001t0002g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172-579_172-578ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199669 | T | TTACGGTC others(149): Show |
43 | a0001c0001t0001g0111 a0001c0001t0002g0001 a0001c0001t0002g0003 others(40): Show |
54 | HG00609.hp1 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.172-579_172-578ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199669 | T | TTACGGTC others(32): Show |
1 | a0001c0001t0002g0310 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-639_172-638ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | ||||||
chr13:114199671 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-654A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199671 | |||||||
chr13:114199675 | T | TCCCCGCT others(150): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0274 |
2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.172-579_172-578ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199675 | ||||||
chr13:114199681 | CTGAGGCG others(188): Show |
C | 3 | a0001c0001t0001g0131 a0001c0001t0002g0278 a0001c0001t0002g0279 |
3 | HG00140.hp2 HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.172-617_172-423del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199681 | ||||||
chr13:114199682 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-643T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199682 | |||||||
chr13:114199687 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(189): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.172-638C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199687 | |||||||
chr13:114199693 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0003g0175 a0001c0001t0006g0332 |
3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-632G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199693 | |||||||
chr13:114199695 | C | G | 7 | a0001c0001t0004g0009 a0001c0001t0004g0244 a0001c0001t0004g0248 others(4): Show |
9 | HG00544.hp2 HG00609.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-630C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199695 | |||||||
chr13:114199695 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0003g0175 a0001c0001t0006g0332 |
3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-630C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199695 | |||||||
chr13:114199697 | C | G | 3 | a0001c0001t0001g0120 a0001c0001t0003g0175 a0001c0001t0006g0332 |
3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-628C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199697 | |||||||
chr13:114199703 | C | T | 63 | a0001c0001t0001g0120 a0001c0001t0003g0006 a0001c0001t0003g0007 others(60): Show |
73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-622C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199703 | |||||||
chr13:114199707 | C | T | 12 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-618C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199707 | |||||||
chr13:114199708 | G | T | 75 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0130 others(72): Show |
89 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-617G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199708 | |||||||
chr13:114199710 | A | T | 3 | a0001c0001t0001g0120 a0001c0001t0003g0175 a0001c0001t0006g0332 |
3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-615A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199710 | |||||||
chr13:114199721 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0010g0317 |
3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172-604T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199721 | |||||||
chr13:114199726 | G | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0034 others(50): Show |
60 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-599G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199726 | |||||||
chr13:114199732 | G | A | 61 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(58): Show |
71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-593G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199732 | |||||||
chr13:114199734 | C | G | 33 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(30): Show |
37 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.172-591C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199734 | |||||||
chr13:114199734 | C | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(57): Show |
70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-591C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199734 | |||||||
chr13:114199736 | C | G | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(57): Show |
70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-589C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199736 | |||||||
chr13:114199736 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-589C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199736 | |||||||
chr13:114199742 | C | T | 66 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(63): Show |
76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.172-583C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199742 | |||||||
chr13:114199743 | G | GTGCTTAC others(1012): Show |
1 | a0001c0001t0002g0300 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(1019): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | ||||||
chr13:114199743 | G | GTGCTTAC others(1008): Show |
1 | a0001c0001t0002g0303 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(1015): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | ||||||
chr13:114199743 | G | GTGCTTAC others(1007): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0307 |
2 | HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.172-579_172-578ins others(1014): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | ||||||
chr13:114199743 | G | T | 1 | a0001c0001t0008g0090 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172-582G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199743 | |||||||
chr13:114199746 | C | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0003g0175 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-579C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199746 | |||||||
chr13:114199746 | C | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(57): Show |
70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-579C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199746 | |||||||
chr13:114199747 | G | T | 28 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(25): Show |
31 | HG00642.hp2 HG01361.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.172-578G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199747 | |||||||
chr13:114199749 | A | ACGGTCCC others(71): Show |
3 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0335 |
6 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-540_172-539ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199749 | ||||||
chr13:114199749 | A | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(57): Show |
70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-576A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199749 | |||||||
chr13:114199760 | T | C | 64 | a0001c0001t0001g0120 a0001c0001t0001g0316 a0001c0001t0003g0006 others(61): Show |
74 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.172-565T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199760 | |||||||
chr13:114199760 | T | TGAGGCGT others(71): Show |
1 | a0001c0001t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.172-561_172-560ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199760 | ||||||
chr13:114199765 | G | C | 135 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(132): Show |
159 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-560G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199765 | |||||||
chr13:114199765 | G | GGTGACGG others(32): Show |
2 | a0001c0001t0002g0011 a0001c0001t0002g0039 |
2 | HG01928.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.172-527_172-489dup others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199765 | ||||||
chr13:114199771 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.172-554G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199771 | |||||||
chr13:114199773 | C | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(20): Show |
30 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.172-552C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199773 | |||||||
chr13:114199775 | C | T | 5 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0337 others(2): Show |
5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-550C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199775 | |||||||
chr13:114199781 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(2): Show |
5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-544C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199781 | |||||||
chr13:114199785 | C | CTTACGGT others(149): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.172-540_172-539ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | |||||||
chr13:114199785 | C | G | 63 | a0001c0001t0001g0316 a0001c0001t0003g0006 a0001c0001t0003g0007 others(60): Show |
73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-540C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | |||||||
chr13:114199785 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0123 others(10): Show |
16 | HG00733.hp1 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.172-540C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | |||||||
chr13:114199786 | G | T | 20 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0162 others(17): Show |
23 | HG00099.hp2 HG00642.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.172-539G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199786 | |||||||
chr13:114199798 | CTGAGGCG others(149): Show |
C | 1 | a0001c0001t0002g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.172-500_172-345del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199798 | ||||||
chr13:114199799 | T | C | 63 | a0001c0001t0001g0316 a0001c0001t0003g0006 a0001c0001t0003g0007 others(60): Show |
73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-526T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199799 | |||||||
chr13:114199804 | C | CGTGACGG others(110): Show |
1 | a0001c0001t0002g0318 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.172-489_172-488ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | CGTGACGG others(71): Show |
9 | a0001c0001t0001g0080 a0001c0001t0001g0265 a0001c0001t0004g0009 others(6): Show |
11 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | CGTGACGG others(305): Show |
3 | a0001c0001t0004g0047 a0001c0001t0004g0230 a0001c0001t0004g0245 |
3 | NA18990.hp1 NA19075.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | CGTGACGG others(305): Show |
3 | a0001c0001t0004g0010 a0001c0001t0004g0033 a0001c0001t0013g0109 |
6 | HG02129.hp2 HG02155.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | CGTGACGG others(344): Show |
4 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0001t0001g0258 others(1): Show |
4 | HG00733.hp2 HG03471.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(351): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | CGTGACGG others(305): Show |
1 | a0001c0001t0004g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | ||||||
chr13:114199804 | C | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(138): Show |
156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-521C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199804 | |||||||
chr13:114199810 | G | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0175 others(3): Show |
6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-515G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199810 | |||||||
chr13:114199812 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0084 others(8): Show |
12 | HG01258.hp2 HG01516.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-513C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199812 | |||||||
chr13:114199812 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0175 others(3): Show |
6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-513C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199812 | |||||||
chr13:114199814 | C | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0192 a0001c0001t0003g0175 others(3): Show |
6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-511C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199814 | |||||||
chr13:114199814 | C | T | 5 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0337 others(2): Show |
5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-511C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199814 | |||||||
chr13:114199820 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
18 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.172-505C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199820 | |||||||
chr13:114199824 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-501C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199824 | |||||||
chr13:114199824 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
42 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.172-501C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199824 | |||||||
chr13:114199825 | G | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(71): Show |
89 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-500G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199825 | |||||||
chr13:114199827 | A | T | 12 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-498A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199827 | |||||||
chr13:114199837 | A | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(333): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.172-488A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199837 | |||||||
chr13:114199838 | T | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0316 a0001c0001t0008g0090 others(1): Show |
4 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-487T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199838 | |||||||
chr13:114199843 | G | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0051 others(30): Show |
35 | HG00099.hp2 HG00558.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.172-482G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199843 | |||||||
chr13:114199843 | G | GGTGACAG others(71): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-477_172-476ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199843 | ||||||
chr13:114199843 | GGTGACGG others(32): Show |
G | 1 | a0001c0001t0002g0037 | 2 | HG00323.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-349_172-311del others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199843 | ||||||
chr13:114199849 | G | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(62): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-476G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199849 | |||||||
chr13:114199851 | C | CGCGTCCC others(32): Show |
1 | a0001c0001t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199851 | ||||||
chr13:114199851 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(62): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-474C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199851 | |||||||
chr13:114199853 | C | CGTCCCTG others(110): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0054 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-467_172-466ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199853 | ||||||
chr13:114199853 | C | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0057 others(62): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-472C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199853 | |||||||
chr13:114199853 | C | T | 1 | a0001c0001t0006g0332 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.172-472C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199853 | |||||||
chr13:114199859 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(56): Show |
69 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.172-466C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199859 | |||||||
chr13:114199860 | G | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0065 others(38): Show |
45 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.172-465G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199860 | |||||||
chr13:114199863 | C | CGTACGGT others(32): Show |
1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | |||||||
chr13:114199863 | C | CGTACGGT others(32): Show |
1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | |||||||
chr13:114199863 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0316 a0001c0001t0010g0317 |
3 | HG01167.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-462C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | |||||||
chr13:114199863 | C | T | 63 | a0001c0001t0001g0084 a0001c0001t0001g0130 a0001c0001t0003g0006 others(60): Show |
73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-462C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | |||||||
chr13:114199864 | T | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
308 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.172-461T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199864 | |||||||
chr13:114199866 | A | T | 61 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(58): Show |
71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-459A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199866 | |||||||
chr13:114199876 | A | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(332): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.172-449A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199876 | |||||||
chr13:114199877 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0316 a0001c0001t0010g0317 |
3 | HG01167.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-448T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199877 | |||||||
chr13:114199882 | C | CGTGACGG others(855): Show |
1 | a0001c0001t0002g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172-411_172-410ins others(862): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | ||||||
chr13:114199882 | C | CGTGACGG others(71): Show |
1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172-436_172-435ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | ||||||
chr13:114199882 | C | CGTGACGG others(110): Show |
1 | a0001c0004t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-436_172-435ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | ||||||
chr13:114199882 | C | CGTGACGG others(149): Show |
1 | a0001c0001t0001g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.172-436_172-435ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | ||||||
chr13:114199882 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(191): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.172-443C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199882 | |||||||
chr13:114199892 | C | T | 4 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0332 others(1): Show |
7 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-433C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199892 | |||||||
chr13:114199898 | C | T | 4 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-427C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199898 | |||||||
chr13:114199902 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-423C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199902 | |||||||
chr13:114199902 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(5): Show |
11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199902 | |||||||
chr13:114199903 | T | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(208): Show |
244 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.172-422T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199903 | |||||||
chr13:114199905 | A | ACGGTCCC others(1046): Show |
2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-411_172-410ins others(1053): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199905 | ||||||
chr13:114199915 | A | C | 339 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.172-410A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199915 | |||||||
chr13:114199916 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-409T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199916 | |||||||
chr13:114199921 | C | G | 121 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(118): Show |
142 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.172-404C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199921 | |||||||
chr13:114199927 | G | A | 5 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(2): Show |
5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-398G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199927 | |||||||
chr13:114199929 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(2): Show |
5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-396C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199929 | |||||||
chr13:114199931 | C | G | 5 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(2): Show |
5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-394C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199931 | |||||||
chr13:114199931 | C | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(5): Show |
11 | HG00642.hp2 HG01993.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-394C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199931 | |||||||
chr13:114199937 | C | T | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(8): Show |
11 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-388C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199937 | |||||||
chr13:114199941 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(16): Show |
22 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-384C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199941 | |||||||
chr13:114199942 | T | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
297 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.172-383T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199942 | |||||||
chr13:114199942 | T | TTACGGTC others(149): Show |
1 | a0001c0001t0006g0332 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.172-372_172-371ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199942 | ||||||
chr13:114199942 | T | TTACGGTC others(71): Show |
4 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0337 others(1): Show |
4 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-372_172-371ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199942 | ||||||
chr13:114199944 | A | T | 5 | a0001c0001t0001g0192 a0001c0001t0003g0162 a0001c0001t0003g0164 others(2): Show |
5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-381A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199944 | |||||||
chr13:114199954 | A | C | 339 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.172-371A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199954 | |||||||
chr13:114199955 | T | C | 4 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-370T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199955 | |||||||
chr13:114199955 | T | TGAGGGGT others(32): Show |
6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-366_172-365ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199955 | ||||||
chr13:114199960 | C | CGTGACGG others(32): Show |
1 | a0001c0001t0002g0322 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.172-346_172-345ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199960 | ||||||
chr13:114199960 | C | G | 8 | a0001c0001t0001g0120 a0001c0001t0006g0013 a0001c0001t0006g0040 others(5): Show |
11 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-365C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199960 | |||||||
chr13:114199966 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-359G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199966 | |||||||
chr13:114199968 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-357C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199968 | |||||||
chr13:114199969 | G | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-356G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199969 | |||||||
chr13:114199970 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-355C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199970 | |||||||
chr13:114199970 | C | T | 3 | a0001c0001t0006g0333 a0001c0001t0006g0334 a0001c0001t0006g0339 |
3 | HG01361.hp2 HG02273.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.172-355C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199970 | |||||||
chr13:114199976 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-349C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199976 | |||||||
chr13:114199980 | C | CT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-343dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199980 | ||||||
chr13:114199980 | C | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-345C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199980 | |||||||
chr13:114199980 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-345C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199980 | |||||||
chr13:114199981 | T | G | 78 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(75): Show |
88 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.172-344T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199981 | |||||||
chr13:114199981 | T | TTACGGTC others(149): Show |
1 | a0001c0001t0006g0333 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.172-333_172-332ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199981 | ||||||
chr13:114199981 | T | TTATGGTC others(32): Show |
5 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0332 others(2): Show |
5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-342_172-341ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199981 | ||||||
chr13:114199983 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-342A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199983 | |||||||
chr13:114199994 | T | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-331T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199994 | |||||||
chr13:114199999 | C | CGTAACAG others(110): Show |
1 | a0001c0001t0006g0339 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.172-324_172-323ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199999 | ||||||
chr13:114199999 | C | G | 11 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(8): Show |
14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-326C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199999 | |||||||
chr13:114200004 | C | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-321C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200004 | |||||||
chr13:114200009 | C | T | 2 | a0001c0001t0006g0334 a0001c0001t0006g0336 |
2 | HG01993.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.172-316C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200009 | |||||||
chr13:114200015 | T | C | 85 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.172-310T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200015 | |||||||
chr13:114200020 | T | G | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-305T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200020 | |||||||
chr13:114200023 | C | T | 7 | a0001c0001t0006g0330 a0001c0001t0006g0331 a0001c0001t0006g0332 others(4): Show |
7 | HG01361.hp2 HG01993.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-302C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200023 | |||||||
chr13:114200038 | G | C | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-287G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200038 | |||||||
chr13:114200044 | A | G | 74 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(71): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-281A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200044 | |||||||
chr13:114200046 | T | C | 74 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(71): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-279T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200046 | |||||||
chr13:114200048 | G | C | 71 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(68): Show |
81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.172-277G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200048 | |||||||
chr13:114200048 | G | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0335 |
6 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-277G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200048 | |||||||
chr13:114200054 | T | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-271T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200054 | |||||||
chr13:114200056 | T | TGCTTACG others(304): Show |
1 | a0001c0001t0006g0334 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.172-268_172-267ins others(311): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200056 | ||||||
chr13:114200056 | T | TGCTTACG others(303): Show |
1 | a0001c0001t0006g0336 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.172-268_172-267ins others(310): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200056 | ||||||
chr13:114200058 | T | C | 72 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(69): Show |
85 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.172-267T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200058 | |||||||
chr13:114200059 | G | T | 72 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(69): Show |
85 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.172-266G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200059 | |||||||
chr13:114200061 | T | A | 74 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(71): Show |
87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-264T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200061 | |||||||
chr13:114200061 | TCGGTCCC others(32): Show |
T | 2 | a0001c0001t0001g0120 a0001c0001t0003g0175 |
2 | HG03225.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.172-252_172-214del others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200061 | ||||||
chr13:114200072 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-253T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200072 | |||||||
chr13:114200073 | T | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.172-252T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200073 | |||||||
chr13:114200077 | G | C | 12 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-248G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200077 | |||||||
chr13:114200083 | G | A | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-242G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200083 | |||||||
chr13:114200085 | C | T | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-240C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200085 | |||||||
chr13:114200087 | T | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(27): Show |
33 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-238T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200087 | |||||||
chr13:114200087 | T | G | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-238T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200087 | |||||||
chr13:114200087 | T | TGTCCCCG others(227): Show |
2 | a0001c0001t0006g0013 a0001c0001t0006g0335 |
2 | HG02273.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.172-179_172-178ins others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200087 | ||||||
chr13:114200093 | C | T | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-232C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200093 | |||||||
chr13:114200097 | C | T | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-228C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200097 | |||||||
chr13:114200098 | T | G | 72 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(69): Show |
82 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.172-227T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200098 | |||||||
chr13:114200100 | A | ACGGTCCC others(111): Show |
1 | a0001c0001t0001g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.172-217_172-216ins others(118): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | ||||||
chr13:114200100 | A | ACGGTCCC others(110): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0088 others(1): Show |
4 | HG03491.hp1 HG03704.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-207_172-206ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | ||||||
chr13:114200100 | A | ACGGTCCC others(266): Show |
2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-210_172-209ins others(273): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | ||||||
chr13:114200100 | A | ACGGTCCC others(188): Show |
3 | a0001c0001t0003g0162 a0001c0001t0003g0164 a0001c0001t0003g0169 |
3 | NA18977.hp1 NA19000.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.172-210_172-209ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | ||||||
chr13:114200100 | A | T | 62 | a0001c0001t0001g0192 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-225A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200100 | |||||||
chr13:114200104 | T | TCCCCGCT others(112): Show |
1 | a0001c0001t0001g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.172-207_172-206ins others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200104 | ||||||
chr13:114200104 | T | TCCCCGCT others(189): Show |
1 | a0001c0001t0003g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.172-210_172-209ins others(196): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200104 | ||||||
chr13:114200141 | G | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(16): Show |
22 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-184G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200141 | |||||||
chr13:114200141 | G | GGTCCCCG others(227): Show |
2 | a0001c0001t0006g0013 a0001c0001t0006g0040 |
4 | HG00642.hp2 HG03834.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-179_172-178ins others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200141 | ||||||
chr13:114200199 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-126T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200199 | |||||||
chr13:114200502 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+59G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200502 | |||||||
chr13:114200503 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290+60G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200503 | |||||||
chr13:114200570 | CA | C | 85 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.290+128delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200570 | |||||||
chr13:114200588 | G | T | 1 | a0001c0001t0002g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.290+145G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200588 | |||||||
chr13:114200794 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+351G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200794 | |||||||
chr13:114200965 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0065 others(38): Show |
45 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+522A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200965 | |||||||
chr13:114201027 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.290+584G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201027 | |||||||
chr13:114201117 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.290+674C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201117 | |||||||
chr13:114201621 | T | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
8 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+1178T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201621 | |||||||
chr13:114201753 | C | T | 1 | a0001c0001t0007g0134 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290+1310C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201753 | |||||||
chr13:114202020 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.290+1577C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202020 | |||||||
chr13:114202021 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+1578G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202021 | |||||||
chr13:114202051 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+1608G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202051 | |||||||
chr13:114202117 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290+1674G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202117 | |||||||
chr13:114202145 | G | A | 1 | a0001c0001t0005g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.290+1702G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202145 | |||||||
chr13:114202160 | A | G | 26 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(23): Show |
29 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.290+1717A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202160 | |||||||
chr13:114202166 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.290+1723C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202166 | |||||||
chr13:114202227 | T | C | 1 | a0001c0001t0003g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.290+1784T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202227 | |||||||
chr13:114202229 | T | G | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+1786T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202229 | |||||||
chr13:114202365 | G | A | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.290+1922G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202365 | |||||||
chr13:114202414 | T | C | 1 | a0001c0001t0005g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290+1971T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202414 | |||||||
chr13:114202577 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
13 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+2134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202577 | |||||||
chr13:114202623 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0129 others(5): Show |
11 | HG01243.hp1 HG01258.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+2180C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202623 | |||||||
chr13:114202635 | T | C | 13 | a0001c0001t0002g0288 a0001c0001t0006g0013 a0001c0001t0006g0040 others(10): Show |
16 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.290+2192T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202635 | |||||||
chr13:114202704 | A | T | 1 | a0001c0001t0003g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.290+2261A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202704 | |||||||
chr13:114202747 | T | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(173): Show |
201 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.290+2304T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202747 | |||||||
chr13:114202771 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
209 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.290+2328T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202771 | |||||||
chr13:114202823 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290+2380C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202823 | |||||||
chr13:114202866 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.290+2423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202866 | |||||||
chr13:114202930 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290+2487A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202930 | |||||||
chr13:114203439 | G | T | 1 | a0001c0001t0002g0297 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290+2996G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203439 | |||||||
chr13:114203677 | A | G | 1 | a0001c0001t0005g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.290+3234A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203677 | |||||||
chr13:114203732 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0076 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+3289C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203732 | |||||||
chr13:114203757 | C | G | 50 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0224 others(47): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.290+3314C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203757 | |||||||
chr13:114203820 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0014 others(83): Show |
101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.290+3377T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203820 | |||||||
chr13:114203892 | C | A | 7 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0118 others(4): Show |
10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3449C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203892 | |||||||
chr13:114203992 | A | G | 1 | a0001c0001t0006g0335 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.290+3549A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203992 | |||||||
chr13:114204158 | A | G | 29 | a0001c0001t0001g0075 a0001c0001t0001g0227 a0001c0001t0005g0018 others(26): Show |
32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.290+3715A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204158 | |||||||
chr13:114204206 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.290+3763A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204206 | |||||||
chr13:114204244 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.290+3801C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204244 | |||||||
chr13:114204358 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0327 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.290+3915G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204358 | |||||||
chr13:114204422 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290+3979T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204422 | |||||||
chr13:114204499 | T | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+4056T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204499 | |||||||
chr13:114204529 | A | G | 1 | a0001c0001t0003g0024 | 2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.290+4086A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204529 | |||||||
chr13:114204622 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+4179G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204622 | |||||||
chr13:114204685 | C | T | 2 | a0001c0001t0002g0037 a0001c0004t0001g0060 |
3 | HG00323.hp2 HG02148.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.290+4242C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204685 | |||||||
chr13:114204776 | G | C | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+4333G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204776 | |||||||
chr13:114204805 | G | T | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+4362G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204805 | |||||||
chr13:114204811 | CAAG | C | 8 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0043 others(5): Show |
10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+4373_290+4375d others(5): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114204811 | ||||||
chr13:114204871 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.290+4428T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204871 | |||||||
chr13:114204961 | C | T | 2 | a0001c0001t0003g0184 a0001c0001t0003g0194 |
2 | NA18972.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.290+4518C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204961 | |||||||
chr13:114205187 | C | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+4744C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205187 | |||||||
chr13:114205254 | A | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+4811A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205254 | |||||||
chr13:114205381 | CA | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0167 |
3 | NA18997.hp2 NA19007.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.290+4940delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114205381 | ||||||
chr13:114205584 | T | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+5141T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205584 | |||||||
chr13:114205648 | C | A | 1 | a0001c0001t0002g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.290+5205C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205648 | |||||||
chr13:114205770 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.290+5327G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205770 | |||||||
chr13:114205980 | G | T | 9 | a0001c0001t0003g0025 a0001c0001t0003g0143 a0001c0001t0003g0147 others(6): Show |
9 | HG00558.hp1 HG02148.hp2 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+5537G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205980 | |||||||
chr13:114206104 | CT | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0029 others(149): Show |
172 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.290+5678delT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114206104 | ||||||
chr13:114206208 | T | G | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+5765T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206208 | |||||||
chr13:114206247 | C | T | 1 | a0001c0001t0004g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.290+5804C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206247 | |||||||
chr13:114206248 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0003g0143 |
2 | HG02148.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.290+5805G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206248 | |||||||
chr13:114206446 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6003C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206446 | |||||||
chr13:114206585 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+6142A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206585 | |||||||
chr13:114206690 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0055 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.290+6247C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206690 | |||||||
chr13:114206708 | T | C | 1 | a0001c0001t0007g0053 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.290+6265T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206708 | |||||||
chr13:114206869 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+6426C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206869 | |||||||
chr13:114206870 | T | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(139): Show |
160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+6427T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206870 | |||||||
chr13:114207021 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6578G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207021 | |||||||
chr13:114207052 | C | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6609C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207052 | |||||||
chr13:114207075 | A | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6632A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207075 | |||||||
chr13:114207106 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+6663C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207106 | |||||||
chr13:114207184 | T | C | 7 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0118 others(4): Show |
10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+6741T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207184 | |||||||
chr13:114207207 | A | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6764A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207207 | |||||||
chr13:114207318 | C | T | 3 | a0001c0001t0002g0303 a0001c0001t0002g0312 a0001c0001t0002g0313 |
3 | HG01099.hp1 HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.290+6875C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207318 | |||||||
chr13:114207453 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.290+7010C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207453 | |||||||
chr13:114207493 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0003g0142 |
2 | HG02698.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.290+7050C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207493 | |||||||
chr13:114207513 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+7070C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207513 | |||||||
chr13:114207590 | C | T | 7 | a0001c0001t0003g0007 a0001c0001t0003g0015 a0001c0001t0003g0118 others(4): Show |
10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+7147C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207590 | |||||||
chr13:114207644 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.290+7201C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207644 | |||||||
chr13:114207814 | C | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(139): Show |
160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+7371C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207814 | |||||||
chr13:114207833 | G | T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(48): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.290+7390G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207833 | |||||||
chr13:114208053 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+7610C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208053 | |||||||
chr13:114208064 | G | A | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+7621G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208064 | |||||||
chr13:114208066 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+7623C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208066 | |||||||
chr13:114208297 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+7854C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208297 | |||||||
chr13:114208298 | G | A | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+7855G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208298 | |||||||
chr13:114208382 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+7939A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208382 | |||||||
chr13:114208447 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+8004C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208447 | |||||||
chr13:114208625 | G | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+8182G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208625 | |||||||
chr13:114208761 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+8318A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208761 | |||||||
chr13:114208822 | T | TA | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.290+8380dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114208822 | ||||||
chr13:114208848 | C | T | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+8405C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208848 | |||||||
chr13:114208885 | C | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0080 others(13): Show |
17 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+8442C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208885 | |||||||
chr13:114208982 | G | T | 1 | a0001c0001t0003g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290+8539G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208982 | |||||||
chr13:114209077 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+8634G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209077 | |||||||
chr13:114209174 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.290+8731C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209174 | |||||||
chr13:114209220 | G | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+8777G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209220 | |||||||
chr13:114209236 | A | G | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+8793A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209236 | |||||||
chr13:114209326 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+8883A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209326 | |||||||
chr13:114209396 | T | C | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+8953T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209396 | |||||||
chr13:114209450 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.290+9007C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209450 | |||||||
chr13:114209499 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.290+9056G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209499 | |||||||
chr13:114209550 | G | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+9107G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209550 | |||||||
chr13:114209619 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+9176G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209619 | |||||||
chr13:114209633 | C | T | 1 | a0001c0001t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.290+9190C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209633 | |||||||
chr13:114209646 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+9203C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209646 | |||||||
chr13:114209648 | G | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+9205G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209648 | |||||||
chr13:114209682 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.290+9239T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209682 | |||||||
chr13:114209723 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.290+9280A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209723 | |||||||
chr13:114209739 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+9296C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209739 | |||||||
chr13:114209751 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(139): Show |
160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+9308C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209751 | |||||||
chr13:114210529 | T | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0341 others(1): Show |
4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+10086T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210529 | |||||||
chr13:114210543 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0205 a0001c0001t0001g0207 others(4): Show |
8 | NA18940.hp2 NA18942.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+10100A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210543 | |||||||
chr13:114210577 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+10134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210577 | |||||||
chr13:114210618 | A | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+10175A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210618 | |||||||
chr13:114210695 | C | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.290+10252C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210695 | |||||||
chr13:114210703 | C | T | 1 | a0001c0001t0002g0275 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.290+10260C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210703 | |||||||
chr13:114210841 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.290+10398G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210841 | |||||||
chr13:114210855 | T | TAC | 63 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0041 others(60): Show |
78 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.290+10447_290+1044 others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACAC | 30 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(27): Show |
32 | HG00140.hp1 HG00408.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.290+10445_290+1044 others(8): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACACAC | 40 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0051 others(37): Show |
45 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.290+10443_290+1044 others(10): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACACACA others(1): Show |
48 | a0001c0001t0001g0101 a0001c0001t0001g0120 a0001c0001t0001g0133 others(45): Show |
54 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.290+10441_290+1044 others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACACACA others(3): Show |
32 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0055 others(29): Show |
39 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.290+10439_290+1044 others(14): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACACACA others(5): Show |
7 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0057 others(4): Show |
8 | HG02257.hp2 HG02258.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+10437_290+1044 others(16): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | T | TACACACA others(7): Show |
3 | a0001c0001t0001g0220 a0001c0001t0003g0144 a0001c0001t0003g0172 |
3 | HG02165.hp1 HG02523.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.290+10435_290+1044 others(18): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210855 | TAC | T | 23 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0067 others(20): Show |
24 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.290+10447_290+1044 others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | ||||||
chr13:114210941 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290+10498G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210941 | |||||||
chr13:114210981 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(179): Show |
206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.290+10538T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210981 | |||||||
chr13:114211058 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+10615A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211058 | |||||||
chr13:114211090 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290+10647G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211090 | |||||||
chr13:114211198 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290+10755C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211198 | |||||||
chr13:114211293 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0130 |
2 | HG01516.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.290+10850G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211293 | |||||||
chr13:114211404 | G | A | 13 | a0001c0001t0001g0034 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.290+10961G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211404 | |||||||
chr13:114211504 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.291-10997C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211504 | |||||||
chr13:114211526 | C | G | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-10975C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211526 | |||||||
chr13:114211526 | C | T | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-10975C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211526 | |||||||
chr13:114211563 | T | TG | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-10935dupG | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114211563 | ||||||
chr13:114211685 | G | A | 1 | a0001c0001t0004g0238 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.291-10816G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211685 | |||||||
chr13:114211722 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.291-10779G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211722 | |||||||
chr13:114211810 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-10691C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211810 | |||||||
chr13:114211820 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.291-10681C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211820 | |||||||
chr13:114211953 | G | A | 2 | a0001c0001t0004g0253 a0001c0001t0013g0109 |
2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.291-10548G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211953 | |||||||
chr13:114211964 | C | T | 1 | a0001c0001t0008g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291-10537C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211964 | |||||||
chr13:114212107 | C | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-10394C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212107 | |||||||
chr13:114212214 | T | C | 1 | a0001c0001t0008g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291-10287T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212214 | |||||||
chr13:114212223 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(44): Show |
52 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.291-10278A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212223 | |||||||
chr13:114212283 | T | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-10218T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212283 | |||||||
chr13:114212307 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.291-10194G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212307 | |||||||
chr13:114212552 | T | TA | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9942dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114212552 | ||||||
chr13:114212695 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.291-9806A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212695 | |||||||
chr13:114212829 | G | A | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-9672G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212829 | |||||||
chr13:114212839 | G | A | 5 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0043 others(2): Show |
7 | HG02451.hp1 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-9662G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212839 | |||||||
chr13:114212847 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9654G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212847 | |||||||
chr13:114212852 | A | AAAAT | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9641_291-9638d others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114212852 | ||||||
chr13:114212985 | T | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9516T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212985 | |||||||
chr13:114212998 | T | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9503T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212998 | |||||||
chr13:114213080 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.291-9421A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213080 | |||||||
chr13:114213133 | C | T | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-9368C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213133 | |||||||
chr13:114213313 | AG | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9187delG | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213313 | |||||||
chr13:114213387 | T | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9114T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213387 | |||||||
chr13:114213446 | C | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-9055C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213446 | |||||||
chr13:114213516 | A | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(178): Show |
205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.291-8985A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213516 | |||||||
chr13:114213547 | C | G | 1 | a0001c0001t0003g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.291-8954C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213547 | |||||||
chr13:114213557 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291-8944C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213557 | |||||||
chr13:114213562 | C | G | 1 | a0001c0001t0003g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.291-8939C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213562 | |||||||
chr13:114213571 | C | G | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8930C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213571 | |||||||
chr13:114213621 | TACCCCTG others(154): Show |
T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-8863_291-8703d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213621 | ||||||
chr13:114213675 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(52): Show |
60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-8826A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213675 | |||||||
chr13:114213734 | C | G | 1 | a0001c0001t0005g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.291-8767C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213734 | |||||||
chr13:114213752 | T | C | 1 | a0001c0001t0004g0230 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.291-8749T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213752 | |||||||
chr13:114213767 | C | T | 38 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(35): Show |
43 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.291-8734C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213767 | |||||||
chr13:114213778 | A | C | 6 | a0001c0001t0006g0013 a0001c0001t0006g0332 a0001c0001t0006g0333 others(3): Show |
8 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-8723A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213778 | |||||||
chr13:114213799 | C | T | 38 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(35): Show |
43 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.291-8702C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213799 | |||||||
chr13:114213821 | GTGGAAGC others(57): Show |
G | 11 | a0001c0001t0006g0013 a0001c0001t0006g0330 a0001c0001t0006g0331 others(8): Show |
13 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-8661_291-8598d others(66): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213821 | ||||||
chr13:114213840 | G | A | 28 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(25): Show |
32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-8661G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213840 | |||||||
chr13:114213844 | C | T | 66 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0015 others(63): Show |
76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.291-8657C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213844 | |||||||
chr13:114213863 | C | T | 1 | a0001c0001t0006g0040 | 2 | NA18999.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291-8638C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213863 | |||||||
chr13:114213873 | A | G | 28 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(25): Show |
32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-8628A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213873 | |||||||
chr13:114213875 | CCCCACCC others(89): Show |
C | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8622_291-8527d others(98): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213875 | ||||||
chr13:114213885 | A | G | 1 | a0001c0001t0006g0040 | 2 | NA18999.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291-8616A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213885 | |||||||
chr13:114213889 | AAGCTCCA others(56): Show |
A | 1 | a0001c0001t0002g0313 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-8611_291-8549d others(65): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213889 | |||||||
chr13:114213953 | G | C | 1 | a0001c0001t0002g0313 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-8548G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213953 | |||||||
chr13:114213977 | T | C | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8524T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213977 | |||||||
chr13:114213982 | G | A | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8519G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213982 | |||||||
chr13:114214012 | G | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8489G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214012 | |||||||
chr13:114214078 | C | T | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291-8423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214078 | |||||||
chr13:114214082 | G | A | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8419G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214082 | |||||||
chr13:114214085 | C | A | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8416C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214085 | |||||||
chr13:114214101 | A | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8400A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214101 | |||||||
chr13:114214115 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-8386C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214115 | |||||||
chr13:114214137 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.291-8364T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214137 | |||||||
chr13:114214243 | G | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8258G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214243 | |||||||
chr13:114214244 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8257C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214244 | |||||||
chr13:114214246 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8255G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214246 | |||||||
chr13:114214247 | G | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8254G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214247 | |||||||
chr13:114214249 | C | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8252C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214249 | |||||||
chr13:114214250 | A | AT | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8250dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214250 | ||||||
chr13:114214267 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8234G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214267 | |||||||
chr13:114214328 | T | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-8173T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214328 | |||||||
chr13:114214372 | A | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-8129A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214372 | |||||||
chr13:114214439 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8062C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214439 | |||||||
chr13:114214582 | T | TTTTG | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
211 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.291-7900_291-7897d others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | ||||||
chr13:114214582 | T | TTTTGTTT others(5): Show |
10 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0043 others(7): Show |
12 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-7908_291-7897d others(14): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | ||||||
chr13:114214582 | T | TTTTGTTT others(9): Show |
16 | a0001c0001t0005g0020 a0001c0001t0005g0044 a0001c0001t0005g0092 others(13): Show |
17 | HG00408.hp1 HG00423.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-7912_291-7897d others(18): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | ||||||
chr13:114214647 | C | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-7854C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214647 | |||||||
chr13:114214728 | A | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0099 a0001c0001t0007g0121 |
4 | HG02572.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-7773A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214728 | |||||||
chr13:114214729 | G | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-7772G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214729 | |||||||
chr13:114214821 | A | C | 1 | a0001c0001t0003g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.291-7680A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214821 | |||||||
chr13:114214912 | CTTAAT | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(82): Show |
98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-7585_291-7581d others(7): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214912 | ||||||
chr13:114214976 | C | T | 67 | a0001c0001t0001g0120 a0001c0001t0003g0006 a0001c0001t0003g0007 others(64): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-7525C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214976 | |||||||
chr13:114215144 | G | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-7357G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215144 | |||||||
chr13:114215145 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-7356C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215145 | |||||||
chr13:114215214 | A | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-7287A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215214 | |||||||
chr13:114215228 | G | C | 1 | a0001c0001t0002g0012 | 3 | NA18957.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.291-7273G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215228 | |||||||
chr13:114215317 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-7184T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215317 | |||||||
chr13:114215518 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-6983T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215518 | |||||||
chr13:114215632 | A | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6869A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215632 | |||||||
chr13:114215751 | C | T | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(16): Show |
22 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-6750C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215751 | |||||||
chr13:114215752 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-6749C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215752 | |||||||
chr13:114215831 | C | T | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-6670C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215831 | |||||||
chr13:114215881 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
251 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.291-6620G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215881 | |||||||
chr13:114215908 | C | A | 1 | a0001c0001t0001g0008 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291-6593C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215908 | |||||||
chr13:114215985 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-6516A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215985 | |||||||
chr13:114215997 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-6504A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215997 | |||||||
chr13:114216215 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6286C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216215 | |||||||
chr13:114216282 | A | G | 1 | a0001c0001t0002g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.291-6219A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216282 | |||||||
chr13:114216332 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0059 others(14): Show |
20 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.291-6169G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216332 | |||||||
chr13:114216478 | A | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6023A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216478 | |||||||
chr13:114216592 | C | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5909C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216592 | |||||||
chr13:114216656 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5845C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216656 | |||||||
chr13:114216670 | T | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5831T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216670 | |||||||
chr13:114216753 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0022 others(6): Show |
12 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-5748G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216753 | |||||||
chr13:114216821 | G | C | 1 | a0001c0001t0002g0306 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.291-5680G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216821 | |||||||
chr13:114216911 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-5590T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216911 | |||||||
chr13:114216939 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(179): Show |
206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.291-5562T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216939 | |||||||
chr13:114217027 | T | G | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-5474T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217027 | |||||||
chr13:114217047 | G | A | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-5454G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217047 | |||||||
chr13:114217132 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5369G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217132 | |||||||
chr13:114217249 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-5252A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217249 | |||||||
chr13:114217383 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(44): Show |
52 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.291-5118A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217383 | |||||||
chr13:114217446 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.291-5055G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217446 | |||||||
chr13:114217601 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-4900G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217601 | |||||||
chr13:114217643 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0203 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.291-4858C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217643 | |||||||
chr13:114217709 | G | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-4792G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217709 | |||||||
chr13:114217801 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0126 |
3 | HG01257.hp2 HG01258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.291-4700A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217801 | |||||||
chr13:114217939 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4562G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217939 | |||||||
chr13:114217944 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4557C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217944 | |||||||
chr13:114217969 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(139): Show |
160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.291-4532A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217969 | |||||||
chr13:114218035 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.291-4466G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218035 | |||||||
chr13:114218105 | G | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-4396G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218105 | |||||||
chr13:114218283 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.291-4218C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218283 | |||||||
chr13:114218294 | AAATACCT others(3): Show |
A | 1 | a0001c0001t0003g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.291-4203_291-4194d others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114218294 | ||||||
chr13:114218316 | C | A | 1 | a0001c0001t0003g0189 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.291-4185C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218316 | |||||||
chr13:114218360 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.291-4141C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218360 | |||||||
chr13:114218405 | C | T | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-4096C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218405 | |||||||
chr13:114218406 | G | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4095G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218406 | |||||||
chr13:114218530 | G | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3971G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218530 | |||||||
chr13:114218541 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-3960G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218541 | |||||||
chr13:114218609 | T | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3892T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218609 | |||||||
chr13:114218701 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.291-3800A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218701 | |||||||
chr13:114218884 | G | A | 74 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(71): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.291-3617G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218884 | |||||||
chr13:114218898 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.291-3603A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218898 | |||||||
chr13:114218922 | G | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3579G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218922 | |||||||
chr13:114219011 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.291-3490G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219011 | |||||||
chr13:114219057 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0122 others(1): Show |
5 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-3444C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219057 | |||||||
chr13:114219097 | G | A | 1 | a0001c0001t0003g0158 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.291-3404G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219097 | |||||||
chr13:114219130 | TGACAAAG others(44): Show |
T | 1 | a0001c0001t0004g0244 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.291-3370_291-3320d others(53): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219130 | |||||||
chr13:114219221 | T | C | 1 | a0001c0001t0002g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.291-3280T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219221 | |||||||
chr13:114219223 | T | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(52): Show |
60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3278T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219223 | |||||||
chr13:114219272 | C | G | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3229C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219272 | |||||||
chr13:114219321 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(52): Show |
60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3180G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219321 | |||||||
chr13:114219408 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(52): Show |
60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3093A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219408 | |||||||
chr13:114219593 | A | T | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-2908A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219593 | |||||||
chr13:114219615 | A | C | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-2886A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219615 | |||||||
chr13:114219713 | C | T | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2788C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219713 | |||||||
chr13:114219755 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-2746G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219755 | |||||||
chr13:114220140 | A | G | 67 | a0001c0001t0001g0120 a0001c0001t0003g0006 a0001c0001t0003g0007 others(64): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-2361A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220140 | |||||||
chr13:114220162 | C | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2339C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220162 | |||||||
chr13:114220163 | C | A | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2338C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220163 | |||||||
chr13:114220173 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0136 |
3 | HG02723.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2328C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220173 | |||||||
chr13:114220239 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2262C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220239 | |||||||
chr13:114220272 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-2229G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220272 | |||||||
chr13:114220381 | G | T | 27 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(24): Show |
33 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.291-2120G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220381 | |||||||
chr13:114220392 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.291-2109C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220392 | |||||||
chr13:114220400 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(51): Show |
59 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.291-2101G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220400 | |||||||
chr13:114220427 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.291-2074T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220427 | |||||||
chr13:114220511 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.291-1990C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220511 | |||||||
chr13:114220756 | C | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0149 others(1): Show |
6 | HG00544.hp1 NA18986.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1745C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220756 | |||||||
chr13:114220773 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0149 others(1): Show |
6 | HG00544.hp1 NA18986.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1728G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220773 | |||||||
chr13:114220818 | T | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-1683T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220818 | |||||||
chr13:114221014 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0010g0317 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-1487C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221014 | |||||||
chr13:114221023 | C | T | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-1478C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221023 | |||||||
chr13:114221134 | C | T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0119 others(48): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-1367C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221134 | |||||||
chr13:114221158 | G | A | 1 | a0001c0001t0007g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-1343G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221158 | |||||||
chr13:114221179 | G | A | 1 | a0001c0001t0005g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.291-1322G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221179 | |||||||
chr13:114221198 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(98): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.291-1303C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221198 | |||||||
chr13:114221223 | G | A | 15 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-1278G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221223 | |||||||
chr13:114221242 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-1259G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221242 | |||||||
chr13:114221379 | G | A | 1 | a0001c0001t0003g0264 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.291-1122G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221379 | |||||||
chr13:114221419 | A | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(39): Show |
50 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.291-1082A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221419 | |||||||
chr13:114221580 | A | G | 42 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(39): Show |
48 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.291-921A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221580 | |||||||
chr13:114221714 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0065 others(26): Show |
33 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.291-787A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221714 | |||||||
chr13:114221762 | G | GA | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.291-730dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114221762 | ||||||
chr13:114221762 | G | GAA | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-731_291-730dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114221762 | ||||||
chr13:114221858 | G | A | 12 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(9): Show |
15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-643G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221858 | |||||||
chr13:114221860 | C | T | 2 | a0001c0001t0009g0328 a0001c0001t0009g0329 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-641C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221860 | |||||||
chr13:114221877 | G | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-624G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221877 | |||||||
chr13:114221886 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0272 a0001c0001t0002g0274 others(3): Show |
8 | HG00609.hp1 HG01099.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-615C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221886 | |||||||
chr13:114221909 | T | C | 13 | a0001c0001t0006g0013 a0001c0001t0006g0040 a0001c0001t0006g0330 others(10): Show |
16 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.291-592T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221909 | |||||||
chr13:114221989 | C | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-512C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221989 | |||||||
chr13:114221993 | G | C | 39 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(36): Show |
45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-508G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221993 | |||||||
chr13:114222083 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(83): Show |
99 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.291-418G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222083 | |||||||
chr13:114222251 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-250T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222251 | |||||||
chr13:114222276 | G | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-225G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222276 | |||||||
chr13:114222468 | G | A | 26 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(23): Show |
29 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.291-33G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222468 |