Item | Value |
---|---|
geneid | 5982 |
ensemblid | ENSG00000049541.11 |
hgncid | 9970 |
symbol | RFC2 |
name | replication factor C subunit 2 |
refseq_nuc | NM_181471.3 |
refseq_prot | NP_852136.1 |
ensembl_nuc | ENST00000055077.8 |
ensembl_prot | ENSP00000055077.3 |
mane_status | MANE Select |
chr | chr7 |
start | 74231502 |
end | 74254399 |
strand | - |
ver | v1.2 |
region | chr7:74231502-74254399 |
region5000 | chr7:74226502-74259399 |
regionname0 | RFC2_chr7_74231502_74254399 |
regionname5000 | RFC2_chr7_74226502_74259399 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 354 | 323 | 88 | 66 | 124 | 14 | 29 | 82 | RFC2_chr7_74226502_74259399 | RFC2 | MEVEA others(349): Show |
chr7 | 74226502 | 74259399 |
a0002 | 0/0 | 354 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | MEVEA others(349): Show |
chr7 | 74226502 | 74259399 |
a0003 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | MEVEA others(349): Show |
chr7 | 74226502 | 74259399 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1062 | 317 | 86 | 63 | 124 | 13 | 29 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0001c0003 | 0/0 | 1062 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0001c0004 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0001c0005 | 0/0 | 1062 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0001c0006 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0001c0008 | 0/0 | 1062 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0002c0002 | 0/0 | 1062 | 2 | 1 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 | ||
a0003c0007 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | ATGGA others(1057): Show |
chr7 | 74226502 | 74259399 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1685 | 281 | 69 | 58 | 111 | 13 | 28 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0002 | 0/0 | 1685 | 16 | 14 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0003 | 0/0 | 1685 | 12 | 0 | 1 | 11 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0004 | 0/0 | 1685 | 2 | 1 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0005 | 0/0 | 1685 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0006 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0008 | 0/0 | 1685 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0001t0009 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AGGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0003t0001 | 0/0 | 1685 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0004t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0005t0001 | 0/0 | 1685 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0006t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0001c0008t0007 | 0/0 | 1685 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0002c0002t0001 | 0/0 | 1685 | 2 | 1 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
a0003c0007t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | AAGAG others(1680): Show |
chr7 | 74226502 | 74259399 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 4 | 7 | 5 | 1 | 3 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 2 | 7 | 0 | 3 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0003 | 0/0 | 12 | 0 | 3 | 7 | 2 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0005 | 0/0 | 6 | 1 | 3 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0010 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0011 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0006t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0001c0008t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
a0003c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00280 | hp1 | a0001 | c0005 | t0001 | g0209 | EUR | FIN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00597 | hp2 | a0001 | c0001 | t0009 | g0221 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0135 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01081 | hp1 | a0001 | c0008 | t0007 | g0219 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01891 | hp2 | a0001 | c0004 | t0002 | g0046 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0175 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | CDX | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02602 | hp2 | a0001 | c0001 | t0008 | g0220 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03195 | hp1 | a0003 | c0007 | t0001 | g0189 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03471 | hp1 | a0001 | c0006 | t0002 | g0038 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0062 | REF | REF | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | RFC2_chr7_74226502_74259399 | RFC2 | chr7 | 74226502 | 74259399 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74238987 | G | A | 1 | a0002 | 2 | HG02572.hp1 HG02698.hp2 |
missense_variant&splice_region_variant | MODERATE | c.695C>T | p.Ala232Val | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/11 | 711/1685 | 695/1065 | 232/354 | chr7 | 74238987 | |||
chr7:74252454 | T | C | 1 | a0003 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.158A>G | p.Asn53Ser | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/11 | 174/1685 | 158/1065 | 53/354 | chr7 | 74252454 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74237413 | T | C | 1 | a0001c0005 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.789A>G | p.Val263Val | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/11 | 805/1685 | 789/1065 | 263/354 | chr7 | 74237413 | |||
chr7:74240030 | T | G | 1 | a0001c0006 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.601A>C | p.Arg201Arg | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/11 | 617/1685 | 601/1065 | 201/354 | chr7 | 74240030 | |||
chr7:74246709 | A | T | 1 | a0001c0004 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.387T>A | p.Thr129Thr | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/11 | 403/1685 | 387/1065 | 129/354 | chr7 | 74246709 | |||
chr7:74249032 | T | C | 1 | a0001c0003 | 2 | HG00735.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.312A>G | p.Glu104Glu | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/11 | 328/1685 | 312/1065 | 104/354 | chr7 | 74249032 | |||
chr7:74254273 | C | T | 1 | a0001c0008 | 1 | HG01081.hp1 | splice_region_variant&synonymous_variant | LOW | c.111G>A | p.Pro37Pro | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/11 | 127/1685 | 111/1065 | 37/354 | chr7 | 74254273 | |||
chr7:74254285 | G | A | 1 | a0001c0008 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.99C>T | p.His33His | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/11 | 115/1685 | 99/1065 | 33/354 | chr7 | 74254285 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74231711 | A | T | 4 | a0001c0001t0002 a0001c0004t0002 a0001c0006t0002 others(1): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*395T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 395 | chr7 | 74231711 | ||||||
chr7:74231782 | C | T | 1 | a0001c0001t0004 | 2 | HG03516.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*324G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 324 | chr7 | 74231782 | ||||||
chr7:74231783 | G | A | 1 | a0001c0001t0005 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*323C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 323 | chr7 | 74231783 | ||||||
chr7:74231847 | T | C | 1 | a0001c0001t0006 | 2 | HG02258.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*259A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 259 | chr7 | 74231847 | ||||||
chr7:74231903 | C | T | 1 | a0001c0008t0007 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 203 | chr7 | 74231903 | ||||||
chr7:74231971 | T | C | 4 | a0001c0001t0002 a0001c0004t0002 a0001c0006t0002 others(1): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 135 | chr7 | 74231971 | ||||||
chr7:74232049 | C | T | 2 | a0001c0001t0003 a0001c0001t0009 |
13 | HG00597.hp2 HG01928.hp2 HG02165.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*57G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 11/11 | 57 | chr7 | 74232049 | ||||||
chr7:74254390 | G | A | 1 | a0001c0001t0008 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/11 | 7 | chr7 | 74254390 | ||||||
chr7:74254398 | T | C | 1 | a0001c0001t0009 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/11 | 15 | chr7 | 74254398 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74232468 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.955-252C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232468 | |||||||
chr7:74232471 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.955-255G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232471 | |||||||
chr7:74232553 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.955-337C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232553 | |||||||
chr7:74232631 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-415A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232631 | |||||||
chr7:74232773 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0085 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.955-557C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232773 | |||||||
chr7:74232804 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.955-588C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74232804 | |||||||
chr7:74233023 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.955-807A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233023 | |||||||
chr7:74233097 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.955-881C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233097 | |||||||
chr7:74233108 | G | C | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.955-892C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233108 | |||||||
chr7:74233202 | C | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-986G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233202 | |||||||
chr7:74233227 | G | T | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-1011C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233227 | |||||||
chr7:74233285 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.955-1069C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233285 | |||||||
chr7:74233433 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.955-1217T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233433 | |||||||
chr7:74233476 | C | T | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.955-1260G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233476 | |||||||
chr7:74233491 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.955-1275C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233491 | |||||||
chr7:74233595 | G | GT | 40 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0029 others(37): Show |
49 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.955-1380dupA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233595 | |||||||
chr7:74233595 | GT | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0097 a0001c0001t0001g0108 others(4): Show |
11 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.955-1380delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233595 | |||||||
chr7:74233596 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.955-1380A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233596 | |||||||
chr7:74233600 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.955-1384A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233600 | |||||||
chr7:74233604 | T | A | 9 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(6): Show |
11 | HG01243.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-1388A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233604 | |||||||
chr7:74233605 | T | A | 1 | a0001c0004t0002g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-1389A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233605 | |||||||
chr7:74233605 | T | G | 1 | a0001c0003t0001g0135 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.955-1389A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233605 | |||||||
chr7:74233833 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-1617G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233833 | |||||||
chr7:74233899 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0147 a0001c0001t0001g0180 |
3 | HG02559.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.954+1633A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74233899 | |||||||
chr7:74234128 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0072 a0001c0001t0001g0075 others(1): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+1404C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234128 | |||||||
chr7:74234154 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.954+1378C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234154 | |||||||
chr7:74234156 | G | A | 6 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(3): Show |
6 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1376C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234156 | |||||||
chr7:74234204 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.954+1328T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234204 | |||||||
chr7:74234266 | T | C | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+1266A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234266 | |||||||
chr7:74234394 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.954+1138A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234394 | |||||||
chr7:74234473 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.954+1059A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234473 | |||||||
chr7:74234634 | T | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.954+898A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74234634 | |||||||
chr7:74235097 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.954+435A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74235097 | |||||||
chr7:74235374 | C | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+158G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74235374 | |||||||
chr7:74235433 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0162 a0001c0001t0001g0166 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.954+99G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74235433 | |||||||
chr7:74235495 | T | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.954+37A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 10/10 | chr7 | 74235495 | |||||||
chr7:74235874 | G | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-229C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74235874 | |||||||
chr7:74235962 | C | T | 48 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(45): Show |
60 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.841-317G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74235962 | |||||||
chr7:74236105 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.841-460A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74236105 | |||||||
chr7:74236235 | C | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.841-590G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74236235 | |||||||
chr7:74236372 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-727G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74236372 | |||||||
chr7:74236864 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.840+498A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74236864 | |||||||
chr7:74236961 | C | CATAA | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+397_840+400dup others(4): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74236961 | |||||||
chr7:74237017 | G | A | 6 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(3): Show |
6 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+345C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74237017 | |||||||
chr7:74237046 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.840+316C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74237046 | |||||||
chr7:74237062 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.840+300C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74237062 | |||||||
chr7:74237067 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.840+295T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74237067 | |||||||
chr7:74237067 | AT | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+294delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 9/10 | chr7 | 74237067 | |||||||
chr7:74237706 | T | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(13): Show |
18 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.760-264A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74237706 | |||||||
chr7:74237888 | A | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.760-446T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74237888 | |||||||
chr7:74237909 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.760-467T>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74237909 | |||||||
chr7:74237910 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.760-468C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74237910 | |||||||
chr7:74238215 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759+708C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238215 | |||||||
chr7:74238301 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.759+622C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238301 | |||||||
chr7:74238709 | A | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+214T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238709 | |||||||
chr7:74238914 | C | T | 1 | a0001c0005t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.759+9G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238914 | |||||||
chr7:74238915 | G | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02630.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.759+8C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238915 | |||||||
chr7:74238920 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | splice_region_variant&intron_variant | LOW | c.759+3A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 8/10 | chr7 | 74238920 | |||||||
chr7:74239155 | C | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0130 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.694-167G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239155 | |||||||
chr7:74239170 | C | CT | 20 | a0001c0001t0001g0028 a0001c0001t0001g0064 a0001c0001t0001g0066 others(17): Show |
21 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.694-183dupA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239170 | |||||||
chr7:74239170 | CT | C | 50 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(47): Show |
62 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.694-183delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239170 | |||||||
chr7:74239278 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.694-290G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239278 | |||||||
chr7:74239352 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.694-364C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239352 | |||||||
chr7:74239457 | G | A | 11 | a0001c0001t0002g0013 a0001c0001t0002g0043 a0001c0001t0002g0044 others(8): Show |
13 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.694-469C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239457 | |||||||
chr7:74239696 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.693+242G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239696 | |||||||
chr7:74239787 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.693+151C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239787 | |||||||
chr7:74239787 | G | C | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+151C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239787 | |||||||
chr7:74239895 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0102 |
3 | HG00741.hp2 HG01123.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.693+43G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 7/10 | chr7 | 74239895 | |||||||
chr7:74240316 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.536-221T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240316 | |||||||
chr7:74240502 | C | CA | 16 | a0001c0001t0001g0014 a0001c0001t0001g0069 a0001c0001t0001g0086 others(13): Show |
18 | HG01081.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.536-408dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240502 | |||||||
chr7:74240502 | C | CAA | 3 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0027 |
10 | HG00408.hp1 HG01257.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.536-409_536-408dup others(2): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240502 | |||||||
chr7:74240502 | CA | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0073 others(15): Show |
20 | HG01243.hp1 HG01256.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.536-408delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240502 | |||||||
chr7:74240521 | A | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(28): Show |
41 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.536-426T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240521 | |||||||
chr7:74240589 | AGGCCTCA others(17): Show |
A | 1 | a0001c0001t0002g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.536-518_536-495del others(24): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240589 | |||||||
chr7:74240590 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0116 |
2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.536-495C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240590 | |||||||
chr7:74240610 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.536-515T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240610 | |||||||
chr7:74240713 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.536-618T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240713 | |||||||
chr7:74240771 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.536-676G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240771 | |||||||
chr7:74240801 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(59): Show |
92 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.536-706A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240801 | |||||||
chr7:74240875 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.536-780G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74240875 | |||||||
chr7:74241168 | G | T | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.536-1073C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241168 | |||||||
chr7:74241311 | C | T | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.536-1216G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241311 | |||||||
chr7:74241580 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.536-1485G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241580 | |||||||
chr7:74241697 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.535+1449G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241697 | |||||||
chr7:74241718 | G | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+1428C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241718 | |||||||
chr7:74241882 | T | G | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+1264A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74241882 | |||||||
chr7:74242167 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.535+979A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242167 | |||||||
chr7:74242749 | T | TA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
90 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.535+396dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242749 | |||||||
chr7:74242749 | TA | T | 18 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0118 others(15): Show |
20 | HG00280.hp1 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.535+396delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242749 | |||||||
chr7:74242789 | T | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.535+357A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242789 | |||||||
chr7:74242816 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.535+330T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242816 | |||||||
chr7:74242922 | C | CA | 14 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0001g0117 others(11): Show |
16 | HG01243.hp1 HG01256.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.535+223dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242922 | |||||||
chr7:74242949 | G | A | 1 | a0001c0004t0002g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.535+197C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74242949 | |||||||
chr7:74243003 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.535+143C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 6/10 | chr7 | 74243003 | |||||||
chr7:74243590 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.435-344G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74243590 | |||||||
chr7:74243604 | CT | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.435-359delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74243604 | |||||||
chr7:74243665 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.435-419T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74243665 | |||||||
chr7:74243757 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.435-511G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74243757 | |||||||
chr7:74244096 | C | CA | 20 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0084 others(17): Show |
22 | HG00621.hp1 HG00741.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.435-851dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244096 | |||||||
chr7:74244096 | CA | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0001g0117 others(3): Show |
6 | HG00323.hp2 HG01081.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-851delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244096 | |||||||
chr7:74244271 | A | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.435-1025T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244271 | |||||||
chr7:74244341 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.435-1095C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244341 | |||||||
chr7:74244348 | TA | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
12 | HG00673.hp2 HG01123.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.435-1103delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244348 | |||||||
chr7:74244360 | A | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.435-1114T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244360 | |||||||
chr7:74244416 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.435-1170G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244416 | |||||||
chr7:74244734 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435-1488C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74244734 | |||||||
chr7:74245029 | AT | A | 7 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0068 others(4): Show |
7 | HG01074.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.434+1632delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245029 | |||||||
chr7:74245186 | C | T | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+1476G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245186 | |||||||
chr7:74245301 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0159 |
2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.434+1361A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245301 | |||||||
chr7:74245356 | T | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.434+1306A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245356 | |||||||
chr7:74245451 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.434+1211T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245451 | |||||||
chr7:74245466 | A | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+1196T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245466 | |||||||
chr7:74245692 | G | A | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+970C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245692 | |||||||
chr7:74245714 | C | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG00741.hp2 HG01123.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.434+948G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245714 | |||||||
chr7:74245714 | C | CA | 20 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0130 others(17): Show |
20 | HG00408.hp2 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.434+947dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245714 | |||||||
chr7:74245826 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.434+836G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245826 | |||||||
chr7:74245878 | T | C | 11 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(8): Show |
13 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.434+784A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74245878 | |||||||
chr7:74246012 | T | C | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.434+650A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246012 | |||||||
chr7:74246059 | G | C | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.434+603C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246059 | |||||||
chr7:74246169 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.434+493G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246169 | |||||||
chr7:74246206 | T | A | 6 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(3): Show |
7 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+456A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246206 | |||||||
chr7:74246214 | T | TAAATAC | 16 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0060 others(13): Show |
18 | HG01884.hp1 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.434+442_434+447dup others(6): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246214 | |||||||
chr7:74246214 | TAAATACA others(5): Show |
T | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.434+436_434+447del others(12): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246214 | |||||||
chr7:74246217 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0133 |
2 | HG00609.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.434+445T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246217 | |||||||
chr7:74246250 | T | G | 1 | a0001c0001t0002g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.434+412A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246250 | |||||||
chr7:74246265 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0218 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.434+397C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246265 | |||||||
chr7:74246398 | C | CA | 14 | a0001c0001t0001g0033 a0001c0001t0001g0059 a0001c0001t0001g0082 others(11): Show |
15 | HG00597.hp2 HG00621.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+263dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246398 | |||||||
chr7:74246398 | CA | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0089 others(2): Show |
9 | HG02895.hp2 HG02922.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.434+263delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246398 | |||||||
chr7:74246414 | C | A | 17 | a0001c0001t0001g0131 a0001c0001t0002g0013 a0001c0001t0002g0039 others(14): Show |
19 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.434+248G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246414 | |||||||
chr7:74246577 | T | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0087 a0001c0001t0001g0141 others(2): Show |
9 | HG00558.hp2 HG00673.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+85A>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 5/10 | chr7 | 74246577 | |||||||
chr7:74246840 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.333-77C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246840 | |||||||
chr7:74246975 | C | CT | 6 | a0001c0001t0001g0201 a0001c0001t0002g0039 a0001c0001t0002g0040 others(3): Show |
6 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.333-213dupA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246975 | |||||||
chr7:74246975 | C | CTT | 30 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(27): Show |
40 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.333-214_333-213dup others(2): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246975 | |||||||
chr7:74246975 | CT | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0132 a0001c0001t0002g0013 others(10): Show |
15 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.333-213delA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246975 | |||||||
chr7:74246993 | T | A | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.333-230A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246993 | |||||||
chr7:74246994 | C | T | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.333-231G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74246994 | |||||||
chr7:74247108 | G | C | 5 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.333-345C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247108 | |||||||
chr7:74247122 | C | CA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0133 others(6): Show |
9 | HG00280.hp1 HG00609.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.333-360dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247122 | |||||||
chr7:74247337 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0005g0024 |
3 | HG01256.hp1 HG01258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.333-574C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247337 | |||||||
chr7:74247409 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.333-646T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247409 | |||||||
chr7:74247524 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.333-761G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247524 | |||||||
chr7:74247562 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.333-799G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247562 | |||||||
chr7:74247639 | CA | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.333-877delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74247639 | |||||||
chr7:74248049 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG00741.hp2 HG01123.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.332+963G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248049 | |||||||
chr7:74248063 | G | A | 1 | a0001c0001t0008g0220 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.332+949C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248063 | |||||||
chr7:74248079 | A | T | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.332+933T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248079 | |||||||
chr7:74248088 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.332+924G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248088 | |||||||
chr7:74248111 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.332+901A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248111 | |||||||
chr7:74248316 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.332+696C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248316 | |||||||
chr7:74248364 | A | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.332+648T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248364 | |||||||
chr7:74248505 | G | GT | 20 | a0001c0001t0001g0161 a0001c0001t0001g0194 a0001c0001t0001g0195 others(17): Show |
22 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.332+506dupA | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248505 | |||||||
chr7:74248536 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.332+476C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248536 | |||||||
chr7:74248573 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(59): Show |
92 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.332+439G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248573 | |||||||
chr7:74248637 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
19 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.332+375C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248637 | |||||||
chr7:74248663 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.332+349T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248663 | |||||||
chr7:74248702 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.332+310T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248702 | |||||||
chr7:74248848 | C | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
12 | HG00673.hp2 HG01123.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.332+164G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 4/10 | chr7 | 74248848 | |||||||
chr7:74249121 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0102 |
2 | HG00741.hp2 HG01123.hp1 |
splice_region_variant&intron_variant | LOW | c.226-3C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 3/10 | chr7 | 74249121 | |||||||
chr7:74249305 | C | A | 1 | a0001c0001t0001g0015 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.226-187G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 3/10 | chr7 | 74249305 | |||||||
chr7:74249362 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.226-244C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 3/10 | chr7 | 74249362 | |||||||
chr7:74249552 | T | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
12 | HG00280.hp1 HG01081.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+187A>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 3/10 | chr7 | 74249552 | |||||||
chr7:74249568 | A | T | 37 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(34): Show |
47 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.225+171T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 3/10 | chr7 | 74249568 | |||||||
chr7:74249785 | G | A | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.184-5C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74249785 | |||||||
chr7:74249793 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184-13A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74249793 | |||||||
chr7:74249897 | G | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0001g0106 others(17): Show |
31 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-117C>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74249897 | |||||||
chr7:74250135 | AG | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-356delC | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250135 | |||||||
chr7:74250155 | AC | A | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.184-376delG | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250155 | |||||||
chr7:74250156 | C | CA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0088 others(3): Show |
8 | HG00741.hp1 HG01934.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-377dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250156 | |||||||
chr7:74250157 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.184-377T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250157 | |||||||
chr7:74250362 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.184-582G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250362 | |||||||
chr7:74250367 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.184-587G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250367 | |||||||
chr7:74250380 | T | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-600A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250380 | |||||||
chr7:74250585 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.184-805A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250585 | |||||||
chr7:74250753 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.184-973C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250753 | |||||||
chr7:74250763 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.184-983G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250763 | |||||||
chr7:74250956 | T | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-1176A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250956 | |||||||
chr7:74250994 | C | G | 1 | a0001c0001t0003g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.184-1214G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74250994 | |||||||
chr7:74251136 | C | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.183+1293G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251136 | |||||||
chr7:74251183 | C | T | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+1246G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251183 | |||||||
chr7:74251460 | G | C | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+969C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251460 | |||||||
chr7:74251537 | C | T | 1 | a0001c0001t0003g0150 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.183+892G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251537 | |||||||
chr7:74251566 | G | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(29): Show |
42 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.183+863C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251566 | |||||||
chr7:74251571 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(108): Show |
153 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.183+858T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251571 | |||||||
chr7:74251633 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.183+796T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251633 | |||||||
chr7:74251659 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.183+770C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251659 | |||||||
chr7:74251717 | A | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.183+712T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251717 | |||||||
chr7:74251755 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0002g0043 |
2 | HG01074.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.183+674C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251755 | |||||||
chr7:74251797 | C | CA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0026 others(9): Show |
19 | HG00140.hp1 HG00438.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.183+631dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251797 | |||||||
chr7:74251797 | CA | C | 18 | a0001c0001t0001g0183 a0001c0001t0002g0013 a0001c0001t0002g0039 others(15): Show |
20 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.183+631delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251797 | |||||||
chr7:74251823 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.183+606G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251823 | |||||||
chr7:74251861 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0142 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.183+568C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251861 | |||||||
chr7:74251864 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0218 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.183+565C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251864 | |||||||
chr7:74251968 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.183+461C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251968 | |||||||
chr7:74251969 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0177 |
2 | HG01934.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.183+460C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251969 | |||||||
chr7:74251992 | C | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.183+437G>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74251992 | |||||||
chr7:74252039 | C | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0090 a0001c0001t0001g0146 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.183+390G>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252039 | |||||||
chr7:74252090 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0044 a0001c0001t0002g0045 others(1): Show |
6 | HG02723.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+339G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252090 | |||||||
chr7:74252098 | C | CA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0149 others(34): Show |
44 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+330dupT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252098 | |||||||
chr7:74252098 | CA | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(49): Show |
82 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.183+330delT | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252098 | |||||||
chr7:74252098 | CAA | C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0212 others(7): Show |
12 | HG01081.hp2 HG01891.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+329_183+330del others(2): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252098 | |||||||
chr7:74252098 | CAAA | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(28): Show |
41 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.183+328_183+330del others(3): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252098 | |||||||
chr7:74252098 | CAAAA | C | 6 | a0001c0001t0001g0192 a0001c0001t0002g0039 a0001c0001t0002g0040 others(3): Show |
6 | HG01081.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+327_183+330del others(4): Show |
RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252098 | |||||||
chr7:74252140 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.183+289C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252140 | |||||||
chr7:74252159 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+270C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252159 | |||||||
chr7:74252174 | G | A | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+255C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252174 | |||||||
chr7:74252193 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.183+236C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252193 | |||||||
chr7:74252295 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.183+134A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252295 | |||||||
chr7:74252362 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.183+67C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 2/10 | chr7 | 74252362 | |||||||
chr7:74252505 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.114-7T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74252505 | |||||||
chr7:74252523 | C | T | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.114-25G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74252523 | |||||||
chr7:74252605 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.114-107T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74252605 | |||||||
chr7:74252647 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.114-149C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74252647 | |||||||
chr7:74252827 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.114-329A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74252827 | |||||||
chr7:74253236 | TG | T | 16 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(13): Show |
18 | HG01081.hp1 HG01243.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-739delC | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253236 | |||||||
chr7:74253292 | G | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0032 others(46): Show |
61 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.114-794C>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253292 | |||||||
chr7:74253438 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.113+833C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253438 | |||||||
chr7:74253569 | A | C | 1 | a0001c0006t0002g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.113+702T>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253569 | |||||||
chr7:74253744 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113+527C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253744 | |||||||
chr7:74253762 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.113+509A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253762 | |||||||
chr7:74253779 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113+492C>T | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253779 | |||||||
chr7:74253860 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.113+411T>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253860 | |||||||
chr7:74253926 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.113+345T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253926 | |||||||
chr7:74253943 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(27): Show |
42 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.113+328A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253943 | |||||||
chr7:74253982 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0040 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.113+289T>C | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74253982 | |||||||
chr7:74254107 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.113+164A>G | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74254107 | |||||||
chr7:74254114 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.113+157G>A | RFC2 | ENSG00000049541.11 | transcript | ENST00000055077.8 | protein_coding | 1/10 | chr7 | 74254114 |