Item | Value |
---|---|
geneid | 92241 |
ensemblid | ENSG00000198771.11 |
hgncid | 28310 |
symbol | RCSD1 |
name | RCSD domain containing 1 |
refseq_nuc | NM_052862.4 |
refseq_prot | NP_443094.3 |
ensembl_nuc | ENST00000367854.8 |
ensembl_prot | ENSP00000356828.3 |
mane_status | MANE Select |
chr | chr1 |
start | 167630232 |
end | 167708696 |
strand | + |
ver | v1.2 |
region | chr1:167630232-167708696 |
region5000 | chr1:167625232-167713696 |
regionname0 | RCSD1_chr1_167630232_167708696 |
regionname5000 | RCSD1_chr1_167625232_167713696 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 416 | 342 | 85 | 55 | 148 | 14 | 38 | 112 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERP others(411): Show |
chr1 | 167625232 | 167713696 |
a0002 | 0/0 | 416 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERP others(411): Show |
chr1 | 167625232 | 167713696 |
a0003 | 0/0 | 416 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERP others(411): Show |
chr1 | 167625232 | 167713696 |
a0004 | 0/0 | 416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERP others(411): Show |
chr1 | 167625232 | 167713696 |
a0005 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERS others(411): Show |
chr1 | 167625232 | 167713696 |
a0006 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | MEERP others(411): Show |
chr1 | 167625232 | 167713696 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1248 | 335 | 81 | 53 | 147 | 14 | 38 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0003 | 0/0 | 1248 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0005 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0008 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0009 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0010 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0001c0011 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0002c0002 | 0/0 | 1248 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0003c0004 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0004c0006 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0005c0012 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 | ||
a0006c0007 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | ATGGA others(1243): Show |
chr1 | 167625232 | 167713696 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5443 | 126 | 24 | 20 | 51 | 6 | 24 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0002 | 0/0 | 5443 | 37 | 2 | 10 | 23 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0003 | 0/0 | 5431 | 36 | 4 | 5 | 20 | 2 | 5 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0004 | 0/0 | 5443 | 24 | 0 | 3 | 16 | 2 | 3 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0005 | 0/0 | 5443 | 10 | 10 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0006 | 0/0 | 5432 | 8 | 4 | 3 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5427): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0007 | 0/0 | 5431 | 7 | 1 | 1 | 3 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0008 | 0/0 | 5447 | 6 | 6 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0009 | 0/0 | 5443 | 4 | 4 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0010 | 0/0 | 5431 | 7 | 0 | 0 | 5 | 1 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0011 | 0/0 | 5431 | 5 | 0 | 3 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0012 | 0/0 | 5443 | 5 | 0 | 0 | 5 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0013 | 0/0 | 5443 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0014 | 0/0 | 5431 | 4 | 0 | 1 | 3 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0015 | 0/0 | 5447 | 4 | 4 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0016 | 0/0 | 5448 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5443): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0017 | 0/0 | 5448 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5443): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0018 | 0/0 | 5447 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0019 | 0/0 | 5432 | 3 | 1 | 1 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5427): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0020 | 0/0 | 5443 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0021 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0022 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0023 | 0/0 | 5443 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0024 | 1/0 | 5443 | 2 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0027 | 0/0 | 5443 | 2 | 0 | 0 | 2 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0028 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0029 | 0/0 | 5442 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5437): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0030 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0031 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0032 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0033 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5427): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0034 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0035 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5424): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0036 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0037 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0038 | 0/0 | 5443 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0039 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0040 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0041 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0042 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0043 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0044 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0045 | 0/0 | 5443 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0046 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0047 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0048 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5427): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0049 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0050 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0051 | 0/0 | 5447 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0052 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0001t0053 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0001c0003t0026 | 0/0 | 5443 | 2 | 1 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0005t0008 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0008t0021 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0001c0009t0005 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0010t0001 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0001c0011t0004 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0002c0002t0009 | 0/0 | 5443 | 3 | 3 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0003c0004t0025 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5442): Show |
chr1 | 167625232 | 167713696 |
a0004c0006t0002 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5438): Show |
chr1 | 167625232 | 167713696 |
a0005c0012t0011 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5426): Show |
chr1 | 167625232 | 167713696 |
a0006c0007t0017 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | CTCTC others(5443): Show |
chr1 | 167625232 | 167713696 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0010g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0011g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0011g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0012g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0012g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0012g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0013g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0013g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0014g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0015g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0015g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0016g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0016g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0016g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0017g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0017g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0018g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0018g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0019g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0020g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0020g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0021g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0022g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0022g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0023g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0024g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0024g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0027g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0028g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0029g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0030g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0031g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0032g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0033g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0034g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0035g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0036g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0037g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0038g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0039g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0040g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0041g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0042g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0043g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0044g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0045g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0046g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0047g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0048g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0049g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0050g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0051g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0052g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0001t0053g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0003t0026g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0003t0026g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0005t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0008t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0009t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0010t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0001c0011t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0002c0002t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0002c0002t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0002c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0003c0004t0025g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0003c0004t0025g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0004c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0005c0012t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
a0006c0007t0017g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0286 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | GBR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00280 | hp2 | a0001 | c0001 | t0047 | g0065 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0127 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0126 | EUR | FIN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00408 | hp1 | a0001 | c0001 | t0051 | g0117 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00423 | hp1 | a0001 | c0001 | t0050 | g0119 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0042 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00544 | hp1 | a0001 | c0001 | t0012 | g0315 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00558 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0182 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01070 | hp1 | a0001 | c0001 | t0034 | g0183 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01074 | hp2 | a0001 | c0001 | t0014 | g0314 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01081 | hp2 | a0001 | c0001 | t0028 | g0335 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01109 | hp1 | a0001 | c0001 | t0024 | g0160 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01109 | hp2 | a0001 | c0003 | t0026 | g0218 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01175 | hp2 | a0001 | c0001 | t0011 | g0043 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01192 | hp2 | a0004 | c0006 | t0002 | g0207 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01243 | hp1 | a0001 | c0001 | t0020 | g0301 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0067 | AMR | PUR | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01255 | hp2 | a0001 | c0001 | t0033 | g0180 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01496 | hp1 | a0001 | c0010 | t0001 | g0012 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0057 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0159 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0248 | EUR | IBS | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01884 | hp1 | a0001 | c0001 | t0040 | g0156 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0339 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01891 | hp2 | a0001 | c0001 | t0044 | g0217 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01928 | hp2 | a0001 | c0001 | t0019 | g0099 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01934 | hp1 | a0001 | c0001 | t0011 | g0274 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02040 | hp2 | a0001 | c0011 | t0004 | g0250 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0326 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02083 | hp2 | a0001 | c0001 | t0037 | g0325 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0153 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0334 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0112 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02280 | hp1 | a0003 | c0004 | t0025 | g0034 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0148 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02451 | hp1 | a0002 | c0002 | t0009 | g0269 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02602 | hp2 | a0001 | c0001 | t0042 | g0215 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0329 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02622 | hp2 | a0001 | c0001 | t0039 | g0337 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0300 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02723 | hp1 | a0001 | c0001 | t0046 | g0058 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0239 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0052 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02818 | hp2 | a0001 | c0001 | t0022 | g0241 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02886 | hp1 | a0005 | c0012 | t0011 | g0234 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02895 | hp1 | a0001 | c0009 | t0005 | g0062 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02895 | hp2 | a0001 | c0001 | t0015 | g0305 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02897 | hp1 | a0001 | c0001 | t0015 | g0304 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02922 | hp1 | a0001 | c0003 | t0026 | g0303 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0327 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02965 | hp1 | a0002 | c0002 | t0009 | g0318 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02976 | hp1 | a0001 | c0008 | t0021 | g0185 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02976 | hp2 | a0003 | c0004 | t0025 | g0240 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03017 | hp1 | a0001 | c0001 | t0010 | g0073 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03041 | hp1 | a0001 | c0001 | t0052 | g0158 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03041 | hp2 | a0001 | c0001 | t0020 | g0317 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03130 | hp1 | a0001 | c0001 | t0018 | g0340 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03139 | hp2 | a0001 | c0001 | t0016 | g0253 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0341 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03225 | hp1 | a0001 | c0001 | t0041 | g0311 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0310 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03453 | hp2 | a0001 | c0001 | t0023 | g0227 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03540 | hp1 | a0006 | c0007 | t0017 | g0242 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03579 | hp2 | a0001 | c0001 | t0022 | g0342 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0118 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03834 | hp2 | a0001 | c0001 | t0045 | g0109 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0142 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04184 | hp2 | a0001 | c0001 | t0038 | g0343 | SAS | BEB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | STU | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18522 | hp2 | a0001 | c0001 | t0019 | g0157 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18906 | hp2 | a0002 | c0002 | t0009 | g0212 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18942 | hp2 | a0001 | c0001 | t0012 | g0277 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18947 | hp1 | a0001 | c0001 | t0027 | g0089 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18947 | hp2 | a0001 | c0001 | t0036 | g0280 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18952 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18956 | hp1 | a0001 | c0001 | t0010 | g0071 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18961 | hp1 | a0001 | c0001 | t0013 | g0198 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18961 | hp2 | a0001 | c0001 | t0049 | g0211 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18970 | hp1 | a0001 | c0001 | t0035 | g0203 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18970 | hp2 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18977 | hp2 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18979 | hp1 | a0001 | c0001 | t0014 | g0177 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18983 | hp1 | a0001 | c0001 | t0013 | g0199 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18984 | hp2 | a0001 | c0001 | t0012 | g0251 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18985 | hp2 | a0001 | c0001 | t0014 | g0181 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0249 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18994 | hp2 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19001 | hp2 | a0001 | c0001 | t0048 | g0102 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19002 | hp1 | a0001 | c0001 | t0032 | g0167 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0077 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19003 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19003 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19005 | hp1 | a0001 | c0001 | t0043 | g0015 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19009 | hp2 | a0001 | c0001 | t0031 | g0172 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19043 | hp1 | a0001 | c0001 | t0053 | g0096 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19043 | hp2 | a0001 | c0001 | t0017 | g0338 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19056 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19057 | hp1 | a0001 | c0001 | t0010 | g0079 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19058 | hp2 | a0001 | c0001 | t0030 | g0191 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19063 | hp2 | a0001 | c0001 | t0012 | g0312 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19067 | hp1 | a0001 | c0001 | t0029 | g0179 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19067 | hp2 | a0001 | c0001 | t0027 | g0078 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | YRI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02486 | hp1 | a0001 | c0001 | t0023 | g0259 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG02559 | hp2 | a0001 | c0005 | t0008 | g0296 | AFR | ACB | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03471 | hp1 | a0001 | c0001 | t0021 | g0005 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG03471 | hp2 | a0001 | c0001 | t0018 | g0330 | AFR | MSL | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | USA | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0074 | REF | REF | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
homoSapiens | grch38p0 | a0001 | c0001 | t0024 | g0232 | REF | REF | RCSD1_chr1_167625232_167713696 | RCSD1 | chr1 | 167625232 | 167713696 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167683906 | C | T | 1 | a0005 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.13C>T | p.Pro5Ser | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/7 | 205/5443 | 13/1251 | 5/416 | chr1 | 167683906 | |||
chr1:167697313 | C | A | 1 | a0004 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.689C>A | p.Thr230Asn | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 881/5443 | 689/1251 | 230/416 | chr1 | 167697313 | |||
chr1:167697469 | C | T | 1 | a0003 | 2 | HG02280.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.845C>T | p.Pro282Leu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1037/5443 | 845/1251 | 282/416 | chr1 | 167697469 | |||
chr1:167697572 | G | C | 2 | a0003 a0006 |
3 | HG02280.hp1 HG02976.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.948G>C | p.Glu316Asp | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1140/5443 | 948/1251 | 316/416 | chr1 | 167697572 | |||
chr1:167697775 | A | G | 1 | a0002 | 3 | HG02451.hp1 HG02965.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1151A>G | p.Gln384Arg | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1343/5443 | 1151/1251 | 384/416 | chr1 | 167697775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167694122 | T | C | 1 | a0001c0003 | 2 | HG01109.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.294T>C | p.Ala98Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 486/5443 | 294/1251 | 98/416 | chr1 | 167694122 | |||
chr1:167694161 | C | T | 1 | a0001c0011 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.333C>T | p.Leu111Leu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 525/5443 | 333/1251 | 111/416 | chr1 | 167694161 | |||
chr1:167694239 | A | G | 1 | a0001c0010 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.411A>G | p.Ala137Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/7 | 603/5443 | 411/1251 | 137/416 | chr1 | 167694239 | |||
chr1:167697296 | G | A | 1 | a0001c0005 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.672G>A | p.Ala224Ala | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 864/5443 | 672/1251 | 224/416 | chr1 | 167697296 | |||
chr1:167697404 | C | T | 1 | a0001c0009 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.780C>T | p.Asn260Asn | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 972/5443 | 780/1251 | 260/416 | chr1 | 167697404 | |||
chr1:167697821 | G | A | 1 | a0001c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1197G>A | p.Glu399Glu | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/7 | 1389/5443 | 1197/1251 | 399/416 | chr1 | 167697821 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167630289 | G | C | 1 | a0001c0001t0028 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 135 | chr1 | 167630289 | ||||||
chr1:167630296 | C | T | 9 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0019 others(6): Show |
41 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | chr1 | 167630296 | |||||||
chr1:167630346 | G | A | 12 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(9): Show |
60 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-78G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 78 | chr1 | 167630346 | ||||||
chr1:167630371 | G | A | 1 | a0001c0001t0036 | 1 | NA18947.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 53 | chr1 | 167630371 | ||||||
chr1:167630408 | T | G | 1 | a0001c0001t0013 | 4 | HG02293.hp1 NA18961.hp1 NA18983.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-16T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/7 | 16 | chr1 | 167630408 | ||||||
chr1:167704779 | C | T | 1 | a0001c0003t0026 | 2 | HG01109.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*83C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 83 | chr1 | 167704779 | ||||||
chr1:167704867 | G | A | 1 | a0001c0001t0037 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 171 | chr1 | 167704867 | ||||||
chr1:167704906 | C | T | 1 | a0003c0004t0025 | 2 | HG02280.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*210C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 210 | chr1 | 167704906 | ||||||
chr1:167705050 | CAGCTAAT others(2): Show |
C | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*359_*367delAATTTA others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 359 | INFO_REALIGN_3_PRIME | chr1 | 167705050 | |||||
chr1:167705066 | T | C | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 370 | chr1 | 167705066 | ||||||
chr1:167705069 | CTAAT | C | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*378delAATT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 375 | INFO_REALIGN_3_PRIME | chr1 | 167705069 | |||||
chr1:167705074 | T | C | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 378 | chr1 | 167705074 | ||||||
chr1:167705075 | T | G | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 379 | chr1 | 167705075 | ||||||
chr1:167705179 | G | C | 1 | a0001c0001t0038 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 483 | chr1 | 167705179 | ||||||
chr1:167705332 | T | TAA | 15 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(12): Show |
78 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*646_*647dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 648 | INFO_REALIGN_3_PRIME | chr1 | 167705332 | |||||
chr1:167705351 | A | T | 3 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0046 |
8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*655A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 655 | chr1 | 167705351 | ||||||
chr1:167705416 | C | G | 15 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(12): Show |
78 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 720 | chr1 | 167705416 | ||||||
chr1:167705432 | C | G | 1 | a0001c0001t0018 | 3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*736C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 736 | chr1 | 167705432 | ||||||
chr1:167705480 | G | A | 2 | a0001c0001t0020 a0001c0001t0039 |
3 | HG01243.hp1 HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*784G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 784 | chr1 | 167705480 | ||||||
chr1:167705540 | G | A | 4 | a0001c0001t0005 a0001c0001t0040 a0001c0003t0026 others(1): Show |
14 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*844G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 844 | chr1 | 167705540 | ||||||
chr1:167705650 | T | C | 2 | a0001c0001t0008 a0001c0005t0008 |
7 | HG01891.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*954T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 954 | chr1 | 167705650 | ||||||
chr1:167705720 | C | T | 1 | a0001c0001t0053 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1024C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1024 | chr1 | 167705720 | ||||||
chr1:167705755 | T | C | 1 | a0001c0003t0026 | 2 | HG01109.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1059 | chr1 | 167705755 | ||||||
chr1:167706172 | T | C | 1 | a0001c0001t0050 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1476 | chr1 | 167706172 | ||||||
chr1:167706298 | A | G | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1602A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1602 | chr1 | 167706298 | ||||||
chr1:167706378 | T | C | 3 | a0001c0001t0011 a0001c0001t0014 a0005c0012t0011 |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1682T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1682 | chr1 | 167706378 | ||||||
chr1:167706412 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(29): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1716T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1716 | chr1 | 167706412 | ||||||
chr1:167706448 | T | C | 2 | a0001c0001t0027 a0001c0001t0043 |
3 | NA18947.hp1 NA19005.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1752T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1752 | chr1 | 167706448 | ||||||
chr1:167706476 | A | ACTTTT | 16 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0016 others(13): Show |
31 | HG00408.hp1 HG01081.hp2 HG01884.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1784_*1785insTCTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1785 | INFO_REALIGN_3_PRIME | chr1 | 167706476 | |||||
chr1:167706509 | T | C | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0021 others(2): Show |
8 | HG02258.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 1813 | chr1 | 167706509 | ||||||
chr1:167706892 | C | T | 1 | a0001c0001t0045 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2196 | chr1 | 167706892 | ||||||
chr1:167706955 | T | C | 4 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0028 others(1): Show |
10 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2259T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2259 | chr1 | 167706955 | ||||||
chr1:167706981 | G | A | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2285G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2285 | chr1 | 167706981 | ||||||
chr1:167707084 | G | A | 5 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0028 others(2): Show |
11 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2388G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2388 | chr1 | 167707084 | ||||||
chr1:167707102 | A | C | 1 | a0001c0001t0049 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2406A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2406 | chr1 | 167707102 | ||||||
chr1:167707127 | C | A | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(26): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2431C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2431 | chr1 | 167707127 | ||||||
chr1:167707174 | T | C | 7 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0017 others(4): Show |
20 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2478T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2478 | chr1 | 167707174 | ||||||
chr1:167707383 | G | A | 1 | a0001c0001t0039 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2687 | chr1 | 167707383 | ||||||
chr1:167707481 | C | T | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(26): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2785C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2785 | chr1 | 167707481 | ||||||
chr1:167707493 | G | GA | 3 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0033 |
12 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2804dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2805 | INFO_REALIGN_3_PRIME | chr1 | 167707493 | |||||
chr1:167707507 | T | C | 1 | a0001c0001t0023 | 2 | HG02486.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2811T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2811 | chr1 | 167707507 | ||||||
chr1:167707564 | C | T | 4 | a0001c0001t0012 a0001c0001t0027 a0001c0001t0031 others(1): Show |
9 | HG00544.hp1 HG00558.hp2 NA18942.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2868C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2868 | chr1 | 167707564 | ||||||
chr1:167707631 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(29): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2935T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2935 | chr1 | 167707631 | ||||||
chr1:167707671 | CT | C | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(26): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2984delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 2984 | INFO_REALIGN_3_PRIME | chr1 | 167707671 | |||||
chr1:167707776 | C | T | 3 | a0001c0001t0009 a0001c0001t0052 a0002c0002t0009 |
8 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3080C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3080 | chr1 | 167707776 | ||||||
chr1:167708054 | A | C | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*3358A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3358 | chr1 | 167708054 | ||||||
chr1:167708121 | C | T | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(5): Show |
55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3425C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3425 | chr1 | 167708121 | ||||||
chr1:167708265 | G | A | 1 | a0003c0004t0025 | 2 | HG02280.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3569G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3569 | chr1 | 167708265 | ||||||
chr1:167708312 | C | T | 1 | a0001c0001t0044 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3616 | chr1 | 167708312 | ||||||
chr1:167708334 | C | T | 1 | a0001c0001t0030 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3638C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3638 | chr1 | 167708334 | ||||||
chr1:167708380 | C | T | 3 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0046 |
8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3684C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3684 | chr1 | 167708380 | ||||||
chr1:167708388 | A | T | 1 | a0001c0001t0042 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3692A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3692 | chr1 | 167708388 | ||||||
chr1:167708407 | C | T | 2 | a0001c0001t0005 a0001c0009t0005 |
11 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3711C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3711 | chr1 | 167708407 | ||||||
chr1:167708410 | G | A | 1 | a0001c0001t0015 | 4 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3714G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3714 | chr1 | 167708410 | ||||||
chr1:167708448 | A | C | 3 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0033 |
12 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3752A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 7/7 | 3752 | chr1 | 167708448 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:167630452 | G | A | 2 | a0001c0001t0003g0004 a0001c0001t0021g0005 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+23G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630452 | |||||||
chr1:167630684 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6+255C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630684 | |||||||
chr1:167630721 | T | TA | 10 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(7): Show |
10 | HG01169.hp1 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+324dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAA | 6 | a0001c0001t0001g0216 a0001c0001t0003g0214 a0001c0001t0009g0213 others(3): Show |
6 | HG01109.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+323_6+324dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAA | 22 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0002g0195 others(19): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.6+322_6+324dupAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAA | 29 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(26): Show |
29 | HG00609.hp2 HG00741.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.6+321_6+324dupAAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0154 others(19): Show |
23 | HG00621.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+320_6+324dupAAAA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAA | 32 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0114 others(29): Show |
32 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.6+319_6+324dupAAAA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA | 28 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(25): Show |
28 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+318_6+324dupAAAA others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(1): Show |
6 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0080 others(3): Show |
6 | HG01255.hp1 NA18945.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+317_6+324dupAAAA others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(3): Show |
5 | a0001c0001t0001g0070 a0001c0001t0004g0072 a0001c0001t0005g0069 others(2): Show |
5 | HG02145.hp2 HG03017.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+315_6+324dupAAAA others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(4): Show |
3 | a0001c0001t0001g0066 a0001c0001t0010g0068 a0001c0001t0011g0067 |
3 | HG01243.hp2 NA18946.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.6+314_6+324dupAAAA others(7): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0005g0061 others(2): Show |
5 | HG00280.hp2 HG00735.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+313_6+324dupAAAA others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(6): Show |
4 | a0001c0001t0001g0059 a0001c0001t0003g0060 a0001c0001t0007g0057 others(1): Show |
4 | HG01515.hp1 HG02723.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+312_6+324dupAAAA others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(7): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0003g0053 others(2): Show |
5 | HG02735.hp2 HG02818.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+311_6+324dupAAAA others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG00099.hp1 HG01981.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+310_6+324dupAAAA others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6+309_6+324dupAAAA others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(10): Show |
4 | a0001c0001t0002g0040 a0001c0001t0003g0041 a0001c0001t0011g0042 others(1): Show |
4 | HG00438.hp2 HG01175.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+308_6+324dupAAAA others(13): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(11): Show |
4 | a0001c0001t0001g0038 a0001c0001t0003g0037 a0001c0001t0003g0039 others(1): Show |
4 | HG02257.hp2 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+307_6+324dupAAAA others(14): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0035 a0003c0004t0025g0034 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6+306_6+324dupAAAA others(15): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0033 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6+305_6+324dupAAAA others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.6+304_6+324dupAAAA others(17): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(15): Show |
2 | a0001c0001t0001g0031 a0001c0001t0005g0030 |
2 | HG02258.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.6+303_6+324dupAAAA others(18): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.6+302_6+324dupAAAA others(19): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(17): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | NA18962.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.6+301_6+324dupAAAA others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(18): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG02055.hp1 HG02083.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+300_6+324dupAAAA others(21): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(19): Show |
3 | a0001c0001t0001g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 |
3 | HG02004.hp2 NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.6+299_6+324dupAAAA others(22): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(20): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0043g0015 |
3 | HG01099.hp1 HG01978.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.6+298_6+324dupAAAA others(23): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(21): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(2): Show |
5 | HG00621.hp2 HG01081.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+297_6+324dupAAAA others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(22): Show |
1 | a0001c0001t0012g0008 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6+296_6+324dupAAAA others(25): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(23): Show |
1 | a0001c0001t0003g0007 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6+295_6+324dupAAAA others(26): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | T | TAAAAAAA others(24): Show |
1 | a0001c0001t0003g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6+294_6+324dupAAAA others(27): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TA | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0254 a0001c0001t0001g0258 others(20): Show |
24 | HG01433.hp1 HG01934.hp1 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+324delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAA | T | 23 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0278 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+323_6+324delAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAA | T | 16 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0302 others(13): Show |
16 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+322_6+324delAAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAA | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0316 a0001c0001t0012g0315 others(3): Show |
7 | HG00544.hp1 HG01074.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+319_6+324delAAAA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0323 others(5): Show |
8 | HG02055.hp2 HG02056.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+317_6+324delAAAA others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0328 a0001c0001t0005g0332 a0001c0001t0008g0329 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+316_6+324delAAAA others(5): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAAA others(3): Show |
T | 12 | a0001c0001t0001g0333 a0001c0001t0001g0336 a0001c0001t0003g0004 others(9): Show |
12 | HG01081.hp2 HG01515.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+315_6+324delAAAA others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0344 a0001c0001t0003g0345 a0001c0001t0038g0343 |
3 | HG03239.hp2 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.6+310_6+324delAAAA others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630721 | TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6+309_6+324delAAAA others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630721 | ||||||
chr1:167630736 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.6+324_6+325insAAAA others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167630736 | ||||||
chr1:167630983 | T | C | 59 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0141 others(56): Show |
59 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.6+554T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167630983 | |||||||
chr1:167631139 | C | T | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+710C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631139 | |||||||
chr1:167631179 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+750T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631179 | |||||||
chr1:167631320 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0328 a0001c0001t0016g0327 |
3 | HG02486.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6+891G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631320 | |||||||
chr1:167631453 | G | A | 11 | a0001c0001t0001g0229 a0001c0001t0001g0320 a0001c0001t0003g0321 others(8): Show |
11 | HG00544.hp1 HG02165.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+1024G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631453 | |||||||
chr1:167631571 | G | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0252 a0001c0001t0001g0272 others(2): Show |
5 | HG01169.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+1142G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631571 | |||||||
chr1:167631581 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0336 a0001c0001t0003g0004 others(15): Show |
19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+1152C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631581 | |||||||
chr1:167631605 | C | T | 84 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(81): Show |
84 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.6+1176C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631605 | |||||||
chr1:167631627 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0103 others(153): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.6+1198A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631627 | |||||||
chr1:167631783 | T | C | 45 | a0001c0001t0002g0121 a0001c0001t0004g0056 a0001c0001t0004g0072 others(42): Show |
45 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+1354T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631783 | |||||||
chr1:167631824 | G | A | 126 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(123): Show |
126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.6+1395G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167631824 | |||||||
chr1:167632209 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0336 a0001c0001t0003g0004 others(15): Show |
19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+1780G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632209 | |||||||
chr1:167632269 | G | A | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6+1840G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632269 | |||||||
chr1:167632316 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(250): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.6+1887A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632316 | |||||||
chr1:167632317 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0016g0327 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6+1888G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632317 | |||||||
chr1:167632450 | A | T | 9 | a0001c0001t0002g0151 a0001c0001t0002g0184 a0001c0001t0002g0206 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+2021A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632450 | |||||||
chr1:167632485 | A | G | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6+2056A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632485 | |||||||
chr1:167632553 | C | G | 5 | a0001c0001t0001g0229 a0001c0001t0001g0320 a0001c0001t0003g0321 others(2): Show |
5 | HG00544.hp1 HG02165.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2124C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632553 | |||||||
chr1:167632580 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6+2151G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632580 | |||||||
chr1:167632647 | A | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(269): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.6+2218A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632647 | |||||||
chr1:167632657 | G | T | 1 | a0001c0001t0004g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6+2228G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632657 | |||||||
chr1:167632686 | TCAC | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(266): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.6+2258_6+2260delCA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632686 | |||||||
chr1:167632691 | TCCAGTAG others(7): Show |
T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(266): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.6+2263_6+2276delCC others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632691 | |||||||
chr1:167632697 | A | T | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2268A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632697 | |||||||
chr1:167632698 | GGTCACTA others(4): Show |
G | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2270_6+2280delGT others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632698 | |||||||
chr1:167632706 | A | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(266): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.6+2277A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632706 | |||||||
chr1:167632708 | CCT | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(266): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.6+2280_6+2281delCT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632708 | |||||||
chr1:167632710 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+2281T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632710 | |||||||
chr1:167632713 | T | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(268): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.6+2284T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632713 | |||||||
chr1:167632714 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(268): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.6+2285C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632714 | |||||||
chr1:167632793 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(250): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.6+2364T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632793 | |||||||
chr1:167632921 | A | G | 1 | a0001c0001t0005g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6+2492A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167632921 | |||||||
chr1:167633025 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0319 a0001c0001t0001g0328 others(18): Show |
22 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+2596A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633025 | |||||||
chr1:167633067 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(250): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.6+2638A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633067 | |||||||
chr1:167633101 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0003g0039 a0001c0005t0008g0296 |
3 | HG02559.hp2 HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.6+2672C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633101 | |||||||
chr1:167633404 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(268): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.6+2975G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633404 | |||||||
chr1:167633429 | C | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0070 |
3 | HG00099.hp1 HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.6+3000C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633429 | |||||||
chr1:167633650 | G | A | 5 | a0001c0001t0001g0229 a0001c0001t0001g0320 a0001c0001t0003g0321 others(2): Show |
5 | HG00544.hp1 HG02165.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3221G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633650 | |||||||
chr1:167633716 | A | G | 2 | a0001c0001t0003g0245 a0001c0001t0006g0271 |
2 | HG01361.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.6+3287A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633716 | |||||||
chr1:167633824 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0005g0332 a0001c0001t0008g0329 others(6): Show |
10 | HG01891.hp1 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+3395C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633824 | |||||||
chr1:167633825 | C | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(330): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.6+3396C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633825 | |||||||
chr1:167633966 | A | G | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.6+3537A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167633966 | |||||||
chr1:167634012 | T | G | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+3583T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634012 | |||||||
chr1:167634045 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0116 others(1): Show |
4 | HG03704.hp2 NA18968.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+3616C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634045 | |||||||
chr1:167634147 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0012g0315 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+3718G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634147 | |||||||
chr1:167634379 | G | GT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0309 a0001c0001t0001g0346 others(3): Show |
6 | HG02074.hp2 HG02145.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+3961dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | ||||||
chr1:167634379 | G | GTT | 8 | a0001c0001t0005g0061 a0001c0001t0008g0219 a0001c0001t0008g0310 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+3960_6+3961dupTT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | ||||||
chr1:167634379 | G | GTTT | 24 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+3959_6+3961dupTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634379 | ||||||
chr1:167634397 | C | A | 3 | a0001c0001t0001g0229 a0001c0001t0012g0315 a0001c0001t0045g0109 |
3 | HG00544.hp1 HG02165.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.6+3968C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634397 | |||||||
chr1:167634520 | T | C | 55 | a0001c0001t0001g0129 a0001c0001t0001g0254 a0001c0001t0001g0272 others(52): Show |
55 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.6+4091T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634520 | |||||||
chr1:167634658 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0028g0335 |
2 | HG01081.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.6+4229T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634658 | |||||||
chr1:167634692 | C | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0233 a0001c0001t0001g0276 others(4): Show |
7 | HG02040.hp2 NA18942.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+4263C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634692 | |||||||
chr1:167634726 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.6+4297G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634726 | |||||||
chr1:167634773 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(207): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.6+4344C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634773 | |||||||
chr1:167634937 | TGA | T | 30 | a0001c0001t0001g0254 a0001c0001t0001g0272 a0001c0001t0002g0040 others(27): Show |
30 | HG01074.hp2 HG01515.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.6+4512_6+4513delAG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634937 | ||||||
chr1:167634939 | AGAGT | A | 7 | a0001c0001t0001g0129 a0001c0001t0002g0141 a0001c0001t0002g0162 others(4): Show |
7 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+4512_6+4515delAG others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634939 | ||||||
chr1:167634941 | A | AGT | 21 | a0001c0001t0001g0279 a0001c0001t0001g0346 a0001c0001t0002g0151 others(18): Show |
21 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+4541_6+4542dupGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | ||||||
chr1:167634941 | A | AGTGT | 5 | a0001c0001t0002g0210 a0001c0001t0006g0295 a0001c0001t0008g0310 others(2): Show |
5 | HG01099.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4539_6+4542dupGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | ||||||
chr1:167634941 | AGT | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0302 a0001c0001t0005g0332 others(8): Show |
11 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.6+4541_6+4542delGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | ||||||
chr1:167634941 | AGTGT | A | 35 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(32): Show |
35 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.6+4539_6+4542delGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | ||||||
chr1:167634941 | AGTGTGTG others(3): Show |
A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(163): Show |
168 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.6+4533_6+4542delGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167634941 | ||||||
chr1:167634947 | T | A | 1 | a0001c0001t0003g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6+4518T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167634947 | |||||||
chr1:167635078 | G | T | 2 | a0001c0001t0002g0146 a0001c0001t0014g0181 |
2 | NA18949.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.6+4649G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635078 | |||||||
chr1:167635402 | CAG | C | 5 | a0001c0001t0001g0139 a0001c0001t0001g0229 a0001c0001t0001g0294 others(2): Show |
5 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+4974_6+4975delAG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635402 | |||||||
chr1:167635751 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6+5322A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635751 | |||||||
chr1:167635957 | C | T | 2 | a0001c0001t0044g0217 a0001c0001t0053g0096 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6+5528C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167635957 | |||||||
chr1:167636022 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6+5593A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636022 | |||||||
chr1:167636099 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0023g0259 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.6+5670T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636099 | |||||||
chr1:167636492 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6+6063G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636492 | |||||||
chr1:167636548 | A | G | 4 | a0001c0001t0001g0263 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | NA18947.hp2 NA18952.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+6119A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636548 | |||||||
chr1:167636580 | G | GTT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0229 others(4): Show |
7 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+6159_6+6160dupTT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167636580 | ||||||
chr1:167636586 | T | G | 3 | a0001c0001t0003g0004 a0001c0001t0015g0304 a0001c0001t0015g0305 |
3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.6+6157T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636586 | |||||||
chr1:167636590 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0003g0011 |
2 | NA18954.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.6+6161G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636590 | |||||||
chr1:167636747 | C | T | 1 | a0001c0001t0008g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6+6318C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636747 | |||||||
chr1:167636772 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+6343G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636772 | |||||||
chr1:167636872 | G | A | 9 | a0001c0001t0001g0139 a0001c0001t0001g0229 a0001c0001t0001g0294 others(6): Show |
9 | HG00280.hp1 HG00544.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+6443G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167636872 | |||||||
chr1:167637014 | C | A | 21 | a0001c0001t0002g0147 a0001c0001t0002g0149 a0001c0001t0002g0150 others(18): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+6585C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637014 | |||||||
chr1:167637154 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6+6725A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637154 | |||||||
chr1:167637156 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6+6727G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637156 | |||||||
chr1:167637313 | G | A | 2 | a0001c0001t0044g0217 a0001c0001t0053g0096 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6+6884G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637313 | |||||||
chr1:167637503 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6+7074G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637503 | |||||||
chr1:167637660 | T | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.6+7231T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637660 | |||||||
chr1:167637730 | C | CCA | 12 | a0001c0001t0001g0231 a0001c0001t0001g0263 a0001c0001t0001g0282 others(9): Show |
12 | HG02074.hp1 HG02109.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7335_6+7336dupAC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | ||||||
chr1:167637730 | C | CCACACAC others(1): Show |
8 | a0001c0001t0001g0279 a0001c0001t0001g0328 a0001c0001t0001g0346 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+7329_6+7336dupAC others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | ||||||
chr1:167637730 | C | CCACACAC others(3): Show |
1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+7327_6+7336dupAC others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | ||||||
chr1:167637730 | CCA | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.6+7335_6+7336delAC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | ||||||
chr1:167637730 | CCACA | C | 12 | a0001c0001t0001g0139 a0001c0001t0001g0229 a0001c0001t0001g0270 others(9): Show |
12 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7333_6+7336delAC others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167637730 | ||||||
chr1:167637972 | G | C | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+7543G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167637972 | |||||||
chr1:167638103 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(251): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.6+7674C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638103 | |||||||
chr1:167638252 | A | T | 22 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(19): Show |
22 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.6+7823A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638252 | |||||||
chr1:167638634 | A | T | 1 | a0001c0001t0002g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+8205A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638634 | |||||||
chr1:167638730 | G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+8301G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638730 | |||||||
chr1:167638872 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
273 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.6+8443A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638872 | |||||||
chr1:167638988 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6+8559A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167638988 | |||||||
chr1:167639013 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.6+8584T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639013 | |||||||
chr1:167639019 | C | G | 66 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(63): Show |
66 | HG00099.hp1 HG00735.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.6+8590C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639019 | |||||||
chr1:167639045 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0047g0065 |
3 | HG00280.hp2 HG01070.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.6+8616A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639045 | |||||||
chr1:167639086 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6+8657A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639086 | |||||||
chr1:167639140 | C | A | 4 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0018g0330 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+8711C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639140 | |||||||
chr1:167639153 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6+8724G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639153 | |||||||
chr1:167639165 | A | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+8736A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | |||||||
chr1:167639165 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.6+8736A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | |||||||
chr1:167639165 | A | T | 4 | a0001c0001t0005g0111 a0001c0001t0016g0112 a0001c0001t0040g0156 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+8736A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639165 | |||||||
chr1:167639173 | C | T | 2 | a0001c0001t0015g0304 a0001c0001t0015g0305 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+8744C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639173 | |||||||
chr1:167639195 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.6+8766T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639195 | |||||||
chr1:167639233 | C | A | 61 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0047 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8804C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639233 | |||||||
chr1:167639234 | A | AGC | 61 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0047 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8805_6+8806insGC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639234 | |||||||
chr1:167639239 | G | A | 61 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0047 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8810G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639239 | |||||||
chr1:167639246 | CAA | C | 61 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0047 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.6+8821_6+8822delAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167639246 | ||||||
chr1:167639248 | A | AAAAC | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.6+8831_6+8834dupCA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167639248 | ||||||
chr1:167639452 | G | A | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+9023G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639452 | |||||||
chr1:167639658 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6+9229A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639658 | |||||||
chr1:167639776 | G | A | 47 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(44): Show |
47 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.6+9347G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639776 | |||||||
chr1:167639790 | G | A | 26 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(23): Show |
26 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+9361G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639790 | |||||||
chr1:167639883 | A | C | 14 | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0001g0254 others(11): Show |
14 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+9454A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167639883 | |||||||
chr1:167640050 | G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+9621G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640050 | |||||||
chr1:167640080 | G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+9651G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640080 | |||||||
chr1:167640112 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0001g0254 others(11): Show |
14 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+9683G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640112 | |||||||
chr1:167640236 | G | A | 7 | a0001c0001t0001g0289 a0001c0001t0001g0302 a0001c0001t0005g0288 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+9807G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640236 | |||||||
chr1:167640237 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.6+9808G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640237 | |||||||
chr1:167640288 | G | A | 6 | a0001c0001t0001g0346 a0001c0001t0003g0313 a0001c0001t0004g0127 others(3): Show |
6 | HG00323.hp1 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+9859G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640288 | |||||||
chr1:167640438 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0033g0180 |
2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.6+10009G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640438 | |||||||
chr1:167640560 | T | C | 1 | a0001c0001t0005g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6+10131T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640560 | |||||||
chr1:167640605 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0064 others(22): Show |
26 | HG00609.hp1 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.6+10176A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640605 | |||||||
chr1:167640693 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0003g0236 a0001c0001t0052g0158 |
3 | HG02896.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6+10264G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640693 | |||||||
chr1:167640713 | G | A | 5 | a0001c0001t0001g0346 a0001c0001t0003g0313 a0001c0001t0004g0127 others(2): Show |
5 | HG00323.hp1 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+10284G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640713 | |||||||
chr1:167640895 | C | T | 1 | a0001c0001t0009g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6+10466C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640895 | |||||||
chr1:167640963 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0054 others(12): Show |
15 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+10534G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640963 | |||||||
chr1:167640981 | C | T | 18 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0054 others(15): Show |
18 | HG00438.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+10552C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640981 | |||||||
chr1:167640988 | C | T | 40 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(37): Show |
40 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.6+10559C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640988 | |||||||
chr1:167640996 | C | G | 1 | a0001c0001t0013g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.6+10567C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167640996 | |||||||
chr1:167641030 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6+10601T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641030 | |||||||
chr1:167641125 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0221 a0001c0001t0003g0236 others(2): Show |
5 | HG02896.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+10696A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641125 | |||||||
chr1:167641205 | A | C | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+10776A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641205 | |||||||
chr1:167641262 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6+10833G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641262 | |||||||
chr1:167641278 | C | A | 1 | a0003c0004t0025g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6+10849C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641278 | |||||||
chr1:167641419 | A | G | 1 | a0001c0001t0004g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.6+10990A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641419 | |||||||
chr1:167641506 | G | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6+11077G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641506 | |||||||
chr1:167641524 | C | G | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+11095C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641524 | |||||||
chr1:167641617 | C | G | 1 | a0001c0001t0003g0345 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6+11188C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641617 | |||||||
chr1:167641725 | A | G | 7 | a0001c0001t0001g0346 a0001c0001t0003g0313 a0001c0001t0004g0127 others(4): Show |
7 | HG00323.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+11296A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641725 | |||||||
chr1:167641748 | C | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+11319C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641748 | |||||||
chr1:167641801 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.6+11372G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641801 | |||||||
chr1:167641948 | G | A | 7 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+11519G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641948 | |||||||
chr1:167641950 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0041g0311 a0001c0003t0026g0303 |
3 | HG02922.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+11521C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641950 | |||||||
chr1:167641984 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11555C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167641984 | |||||||
chr1:167642133 | A | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.6+11704A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642133 | |||||||
chr1:167642171 | C | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0221 a0001c0001t0003g0236 others(4): Show |
7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+11742C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642171 | |||||||
chr1:167642171 | C | T | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+11742C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642171 | |||||||
chr1:167642251 | C | T | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+11822C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642251 | |||||||
chr1:167642314 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11885G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642314 | |||||||
chr1:167642324 | GTGTTTA | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11897_6+11902del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167642324 | ||||||
chr1:167642331 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.6+11902T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642331 | |||||||
chr1:167642522 | C | T | 1 | a0001c0001t0014g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.6+12093C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642522 | |||||||
chr1:167642589 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.6+12160T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642589 | |||||||
chr1:167642645 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6+12216T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642645 | |||||||
chr1:167642672 | C | T | 27 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(24): Show |
27 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.6+12243C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642672 | |||||||
chr1:167642673 | G | A | 2 | a0001c0001t0001g0033 a0001c0003t0026g0303 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+12244G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642673 | |||||||
chr1:167642715 | T | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
17 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+12286T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642715 | |||||||
chr1:167642735 | C | A | 7 | a0001c0001t0001g0346 a0001c0001t0003g0313 a0001c0001t0004g0127 others(4): Show |
7 | HG00323.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+12306C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642735 | |||||||
chr1:167642754 | T | A | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+12325T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642754 | |||||||
chr1:167642808 | A | G | 6 | a0001c0001t0001g0289 a0001c0001t0001g0302 a0001c0001t0001g0328 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+12379A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642808 | |||||||
chr1:167642925 | C | T | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+12496C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642925 | |||||||
chr1:167642940 | G | T | 2 | a0001c0001t0001g0287 a0001c0010t0001g0012 |
2 | HG01169.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.6+12511G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642940 | |||||||
chr1:167642962 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.6+12533T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642962 | |||||||
chr1:167642978 | G | A | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+12549G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167642978 | |||||||
chr1:167643049 | C | T | 2 | a0001c0001t0015g0304 a0001c0001t0015g0305 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+12620C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643049 | |||||||
chr1:167643051 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6+12622C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643051 | |||||||
chr1:167643460 | C | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0081 others(70): Show |
74 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.6+13031C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643460 | |||||||
chr1:167643645 | ATGGC | A | 15 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0152 others(12): Show |
15 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+13220_6+13223del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167643645 | ||||||
chr1:167643775 | G | A | 42 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(39): Show |
42 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.6+13346G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643775 | |||||||
chr1:167643800 | G | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0221 a0001c0001t0003g0236 others(3): Show |
6 | HG02572.hp2 HG02896.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+13371G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643800 | |||||||
chr1:167643800 | G | T | 1 | a0001c0001t0016g0327 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6+13371G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643800 | |||||||
chr1:167643912 | G | A | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+13483G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643912 | |||||||
chr1:167643994 | C | T | 1 | a0001c0001t0003g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6+13565C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167643994 | |||||||
chr1:167644182 | T | C | 67 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0101 others(64): Show |
67 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.6+13753T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644182 | |||||||
chr1:167644246 | G | A | 6 | a0001c0001t0001g0289 a0001c0001t0001g0302 a0001c0001t0001g0328 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+13817G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644246 | |||||||
chr1:167644347 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0221 a0001c0001t0003g0236 others(4): Show |
7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+13918T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644347 | |||||||
chr1:167644366 | C | T | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+13937C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644366 | |||||||
chr1:167644401 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0007g0057 |
2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+13972C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644401 | |||||||
chr1:167644482 | A | AAAAT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0132 a0001c0001t0001g0221 others(8): Show |
11 | HG02155.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+14059_6+14062dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644482 | ||||||
chr1:167644482 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0254 a0001c0001t0002g0195 a0001c0001t0003g0230 others(6): Show |
9 | HG01981.hp2 HG03491.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+14055_6+14062dup others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644482 | ||||||
chr1:167644488 | A | AATAAATA others(5): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0152 others(2): Show |
5 | HG01934.hp2 HG01978.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+14062_6+14063ins others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | ||||||
chr1:167644488 | AATAC | A | 95 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0046 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.6+14106_6+14109del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | ||||||
chr1:167644488 | AATACATA others(1): Show |
A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.6+14102_6+14109del others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | ||||||
chr1:167644488 | AATACATA others(5): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6+14098_6+14109del others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | ||||||
chr1:167644488 | AATACATA others(13): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14090_6+14109del others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167644488 | ||||||
chr1:167644492 | C | A | 31 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(28): Show |
31 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.6+14063C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644492 | |||||||
chr1:167644496 | C | A | 43 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(40): Show |
43 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.6+14067C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644496 | |||||||
chr1:167644500 | C | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.6+14071C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644500 | |||||||
chr1:167644504 | C | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
176 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.6+14075C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644504 | |||||||
chr1:167644508 | C | A | 1 | a0001c0001t0001g0344 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6+14079C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644508 | |||||||
chr1:167644512 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14083C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644512 | |||||||
chr1:167644516 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6+14087C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644516 | |||||||
chr1:167644523 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0221 a0001c0001t0003g0236 others(4): Show |
7 | HG02572.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+14094A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644523 | |||||||
chr1:167644912 | A | T | 2 | a0001c0001t0002g0045 a0001c0001t0007g0057 |
2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+14483A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644912 | |||||||
chr1:167644914 | G | A | 3 | a0001c0001t0015g0304 a0001c0001t0015g0305 a0001c0001t0028g0335 |
3 | HG01081.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6+14485G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167644914 | |||||||
chr1:167645082 | TG | T | 12 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0054 others(9): Show |
12 | HG00438.hp2 HG01175.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+14654delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645082 | |||||||
chr1:167645301 | C | G | 3 | a0001c0001t0008g0219 a0001c0001t0015g0052 a0001c0001t0046g0058 |
3 | HG02723.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.6+14872C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645301 | |||||||
chr1:167645404 | G | A | 16 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+14975G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645404 | |||||||
chr1:167645405 | A | C | 1 | a0001c0001t0003g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6+14976A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645405 | |||||||
chr1:167645405 | A | G | 16 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00438.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+14976A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645405 | |||||||
chr1:167645438 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+15009A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645438 | |||||||
chr1:167645441 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
248 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.6+15012T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645441 | |||||||
chr1:167645508 | G | A | 20 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15079G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645508 | |||||||
chr1:167645515 | A | G | 20 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15086A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645515 | |||||||
chr1:167645536 | C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+15107C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645536 | |||||||
chr1:167645700 | C | A | 1 | a0001c0001t0009g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+15271C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645700 | |||||||
chr1:167645716 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+15287C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645716 | |||||||
chr1:167645764 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6+15335C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645764 | |||||||
chr1:167645841 | G | A | 20 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.6+15412G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645841 | |||||||
chr1:167645965 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6+15536C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167645965 | |||||||
chr1:167646047 | G | A | 9 | a0001c0001t0001g0279 a0001c0001t0001g0287 a0001c0001t0003g0004 others(6): Show |
9 | HG01169.hp2 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+15618G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646047 | |||||||
chr1:167646131 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+15702T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646131 | |||||||
chr1:167646256 | C | G | 1 | a0001c0001t0006g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6+15827C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646256 | |||||||
chr1:167646281 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6+15852C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646281 | |||||||
chr1:167646298 | A | G | 4 | a0001c0001t0003g0004 a0001c0001t0015g0304 a0001c0001t0015g0305 others(1): Show |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+15869A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646298 | |||||||
chr1:167646446 | TA | T | 56 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0108 others(53): Show |
56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.6+16037delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | ||||||
chr1:167646446 | TAA | T | 25 | a0001c0001t0001g0139 a0001c0001t0001g0336 a0001c0001t0001g0346 others(22): Show |
25 | HG00280.hp1 HG01081.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+16036_6+16037del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | ||||||
chr1:167646446 | TAAAA | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0287 a0001c0001t0001g0289 others(8): Show |
11 | HG01070.hp2 HG01169.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+16034_6+16037del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646446 | ||||||
chr1:167646464 | A | G | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6+16035A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646464 | |||||||
chr1:167646505 | TTTTTTC | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
281 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.6+16100_6+16105del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167646505 | ||||||
chr1:167646566 | C | T | 5 | a0001c0001t0003g0236 a0001c0001t0052g0158 a0001c0003t0026g0218 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+16137C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646566 | |||||||
chr1:167646594 | C | T | 6 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0015g0239 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+16165C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646594 | |||||||
chr1:167646649 | A | C | 4 | a0001c0001t0001g0220 a0001c0001t0001g0275 a0001c0001t0003g0256 others(1): Show |
4 | HG00558.hp1 HG00673.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+16220A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646649 | |||||||
chr1:167646661 | C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+16232C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646661 | |||||||
chr1:167646786 | C | T | 1 | a0001c0001t0019g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6+16357C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646786 | |||||||
chr1:167646795 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
285 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.6+16366T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646795 | |||||||
chr1:167646796 | G | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+16367G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646796 | |||||||
chr1:167646928 | A | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0107 a0001c0001t0001g0137 others(18): Show |
21 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+16499A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167646928 | |||||||
chr1:167647072 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(100): Show |
105 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.6+16643G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647072 | |||||||
chr1:167647130 | C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0101 others(25): Show |
28 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | ||||||
chr1:167647130 | C | CAAAAAAA others(4): Show |
232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(229): Show |
234 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | ||||||
chr1:167647130 | C | CAAAAAAA others(5): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0287 others(17): Show |
21 | HG01109.hp2 HG01169.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+16710_6+16711ins others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | ||||||
chr1:167647130 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6+16710_6+16711ins others(13): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647130 | ||||||
chr1:167647264 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6+16835T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647264 | |||||||
chr1:167647317 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
291 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.6+16888A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647317 | |||||||
chr1:167647372 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6+16943T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647372 | |||||||
chr1:167647420 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0006g0223 |
2 | HG01433.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.6+16991C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647420 | |||||||
chr1:167647425 | C | CA | 49 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0103 others(46): Show |
49 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.6+17010dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167647425 | ||||||
chr1:167647483 | G | T | 3 | a0001c0001t0001g0139 a0001c0001t0004g0127 a0001c0001t0045g0109 |
3 | HG00280.hp1 HG00323.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+17054G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647483 | |||||||
chr1:167647601 | C | A | 43 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0103 others(40): Show |
43 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.6+17172C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647601 | |||||||
chr1:167647788 | T | C | 3 | a0001c0001t0001g0279 a0001c0001t0020g0301 a0001c0001t0039g0337 |
3 | HG01243.hp1 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6+17359T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647788 | |||||||
chr1:167647850 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+17421C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647850 | |||||||
chr1:167647877 | A | T | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6+17448A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647877 | |||||||
chr1:167647903 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+17474A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167647903 | |||||||
chr1:167648029 | CA | C | 3 | a0001c0001t0001g0346 a0001c0001t0016g0253 a0003c0004t0025g0034 |
3 | HG02145.hp1 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6+17601delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648029 | |||||||
chr1:167648088 | T | C | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+17659T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648088 | |||||||
chr1:167648146 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0021 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+17717C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648146 | |||||||
chr1:167648201 | A | G | 10 | a0001c0001t0001g0035 a0001c0001t0003g0236 a0001c0001t0008g0262 others(7): Show |
10 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+17772A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648201 | |||||||
chr1:167648254 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6+17825T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648254 | |||||||
chr1:167648298 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+17869T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648298 | |||||||
chr1:167648462 | A | G | 41 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0107 others(38): Show |
41 | HG01109.hp2 HG01934.hp2 HG01978.hp2 others(38): Show |
intron_variant | MODIFIER | c.6+18033A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648462 | |||||||
chr1:167648512 | G | A | 5 | a0001c0001t0001g0346 a0001c0001t0003g0313 a0001c0001t0016g0253 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+18083G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648512 | |||||||
chr1:167648523 | G | C | 3 | a0001c0001t0001g0139 a0001c0001t0004g0127 a0001c0001t0045g0109 |
3 | HG00280.hp1 HG00323.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+18094G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648523 | |||||||
chr1:167648540 | G | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.6+18111G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648540 | |||||||
chr1:167648585 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0002g0168 others(1): Show |
4 | NA18945.hp1 NA18973.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18156G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648585 | |||||||
chr1:167648621 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0003g0236 a0001c0001t0008g0262 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+18192C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648621 | |||||||
chr1:167648688 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6+18259C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648688 | |||||||
chr1:167648694 | TG | T | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+18269delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167648694 | ||||||
chr1:167648710 | G | C | 1 | a0001c0001t0004g0087 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6+18281G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648710 | |||||||
chr1:167648803 | G | A | 6 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0015g0239 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+18374G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648803 | |||||||
chr1:167648819 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0002g0149 a0001c0001t0002g0150 others(7): Show |
10 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+18390A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648819 | |||||||
chr1:167648827 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6+18398C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648827 | |||||||
chr1:167648845 | G | C | 1 | a0001c0001t0012g0008 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6+18416G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648845 | |||||||
chr1:167648883 | C | T | 14 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0254 others(11): Show |
14 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+18454C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648883 | |||||||
chr1:167648933 | T | C | 73 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0101 others(70): Show |
73 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.6+18504T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648933 | |||||||
chr1:167648979 | A | C | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.6+18550A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167648979 | |||||||
chr1:167649038 | T | A | 2 | a0001c0001t0001g0033 a0001c0003t0026g0303 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+18609T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649038 | |||||||
chr1:167649045 | T | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0319 a0001c0001t0020g0317 others(1): Show |
5 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+18616T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649045 | |||||||
chr1:167649123 | A | G | 4 | a0001c0001t0003g0004 a0001c0001t0015g0304 a0001c0001t0015g0305 others(1): Show |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18694A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649123 | |||||||
chr1:167649231 | G | A | 4 | a0001c0001t0001g0328 a0001c0001t0005g0237 a0001c0001t0005g0243 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+18802G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649231 | |||||||
chr1:167649269 | T | C | 4 | a0001c0001t0003g0004 a0001c0001t0015g0304 a0001c0001t0015g0305 others(1): Show |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+18840T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649269 | |||||||
chr1:167649330 | T | C | 15 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0152 others(12): Show |
15 | HG01934.hp2 HG01978.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+18901T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649330 | |||||||
chr1:167649380 | C | T | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+18951C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649380 | |||||||
chr1:167649538 | G | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0238 a0001c0001t0005g0332 others(6): Show |
9 | HG02723.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+19109G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649538 | |||||||
chr1:167649587 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0001g0302 a0001c0001t0005g0288 others(2): Show |
5 | HG02559.hp2 HG02647.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+19158C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649587 | |||||||
chr1:167649588 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6+19159G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649588 | |||||||
chr1:167649634 | G | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.6+19205G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649634 | |||||||
chr1:167649715 | G | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0328 a0001c0001t0005g0237 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+19286G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649715 | |||||||
chr1:167649724 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6+19295G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649724 | |||||||
chr1:167649792 | G | A | 1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6+19363G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649792 | |||||||
chr1:167649904 | C | T | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+19475C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167649904 | |||||||
chr1:167650089 | T | C | 1 | a0001c0001t0009g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6+19660T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650089 | |||||||
chr1:167650096 | C | T | 34 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(31): Show |
34 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.6+19667C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650096 | |||||||
chr1:167650153 | A | C | 3 | a0001c0001t0001g0287 a0001c0001t0023g0227 a0001c0010t0001g0012 |
3 | HG01169.hp2 HG01496.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6+19724A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650153 | |||||||
chr1:167650339 | G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+19910G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650339 | |||||||
chr1:167650514 | G | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+20085G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650514 | |||||||
chr1:167650745 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.6+20316C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650745 | |||||||
chr1:167650782 | C | T | 26 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0103 others(23): Show |
26 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+20353C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650782 | |||||||
chr1:167650972 | G | A | 2 | a0001c0001t0001g0033 a0001c0003t0026g0303 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+20543G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167650972 | |||||||
chr1:167651056 | C | G | 3 | a0001c0001t0001g0287 a0001c0001t0023g0227 a0001c0010t0001g0012 |
3 | HG01169.hp2 HG01496.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6+20627C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651056 | |||||||
chr1:167651122 | G | A | 70 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0101 others(67): Show |
70 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.6+20693G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651122 | |||||||
chr1:167651136 | T | G | 6 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0015g0239 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+20707T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651136 | |||||||
chr1:167651237 | T | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0328 a0001c0001t0005g0237 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+20808T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651237 | |||||||
chr1:167651367 | C | T | 5 | a0001c0001t0008g0310 a0001c0001t0008g0329 a0001c0001t0008g0331 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+20938C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651367 | |||||||
chr1:167651422 | A | C | 1 | a0001c0001t0004g0094 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.6+20993A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651422 | |||||||
chr1:167651472 | C | A | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+21043C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651472 | |||||||
chr1:167651494 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0328 a0001c0001t0005g0237 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+21065C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651494 | |||||||
chr1:167651666 | G | C | 72 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0101 others(69): Show |
72 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.6+21237G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651666 | |||||||
chr1:167651702 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6+21273G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651702 | |||||||
chr1:167651791 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6+21362C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651791 | |||||||
chr1:167651801 | A | T | 9 | a0001c0001t0001g0221 a0001c0001t0001g0238 a0001c0001t0005g0332 others(6): Show |
9 | HG02723.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+21372A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651801 | |||||||
chr1:167651837 | C | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6+21408C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651837 | |||||||
chr1:167651859 | G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6+21430G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651859 | |||||||
chr1:167651907 | T | C | 73 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(70): Show |
73 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+21478T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651907 | |||||||
chr1:167651956 | C | T | 4 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+21527C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167651956 | |||||||
chr1:167652018 | C | CTT | 12 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0003g0134 others(9): Show |
12 | HG01169.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.6+21609_6+21610dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | ||||||
chr1:167652018 | C | CTTT | 32 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0103 others(29): Show |
32 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.6+21608_6+21610dup others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | ||||||
chr1:167652018 | C | CTTTT | 21 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0137 others(18): Show |
21 | HG01884.hp2 HG01934.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.6+21607_6+21610dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | ||||||
chr1:167652018 | C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+21589C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652018 | |||||||
chr1:167652018 | CT | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.6+21610delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652018 | ||||||
chr1:167652123 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0007g0057 |
2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.6+21694G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652123 | |||||||
chr1:167652170 | C | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+21741C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652170 | |||||||
chr1:167652177 | A | G | 2 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.6+21748A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652177 | |||||||
chr1:167652194 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0328 a0001c0001t0005g0237 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+21765G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652194 | |||||||
chr1:167652301 | C | T | 3 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6+21872C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652301 | |||||||
chr1:167652445 | A | G | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+22016A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652445 | |||||||
chr1:167652599 | A | G | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+22170A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652599 | |||||||
chr1:167652633 | A | G | 73 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(70): Show |
73 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+22204A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652633 | |||||||
chr1:167652663 | G | C | 18 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0328 others(15): Show |
18 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.6+22234G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652663 | |||||||
chr1:167652712 | A | AT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.6+22292dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167652712 | ||||||
chr1:167652727 | T | C | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6+22298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652727 | |||||||
chr1:167652762 | A | G | 2 | a0001c0001t0001g0033 a0001c0003t0026g0303 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+22333A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652762 | |||||||
chr1:167652766 | T | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+22337T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652766 | |||||||
chr1:167652767 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.6+22338G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652767 | |||||||
chr1:167652775 | G | A | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6+22346G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652775 | |||||||
chr1:167652882 | T | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(41): Show |
44 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.6+22453T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652882 | |||||||
chr1:167652933 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.6+22504A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652933 | |||||||
chr1:167652952 | T | G | 7 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0005g0288 others(4): Show |
7 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+22523T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652952 | |||||||
chr1:167652953 | A | T | 7 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0005g0288 others(4): Show |
7 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+22524A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652953 | |||||||
chr1:167652985 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0294 |
2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6+22556G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167652985 | |||||||
chr1:167653334 | C | T | 5 | a0001c0001t0008g0310 a0001c0001t0008g0329 a0001c0001t0008g0331 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+22905C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653334 | |||||||
chr1:167653381 | T | C | 5 | a0001c0001t0008g0310 a0001c0001t0008g0329 a0001c0001t0008g0331 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+22952T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653381 | |||||||
chr1:167653494 | T | C | 1 | a0001c0001t0023g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6+23065T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653494 | |||||||
chr1:167653818 | T | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0106 a0001c0001t0010g0077 others(3): Show |
6 | HG02523.hp2 NA18947.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+23389T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653818 | |||||||
chr1:167653983 | G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+23554G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167653983 | |||||||
chr1:167654045 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0003g0267 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.6+23616G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654045 | |||||||
chr1:167654050 | A | T | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6+23621A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654050 | |||||||
chr1:167654083 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.6+23654G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654083 | |||||||
chr1:167654151 | T | C | 34 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0107 others(31): Show |
34 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.6+23722T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654151 | |||||||
chr1:167654165 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+23736G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654165 | |||||||
chr1:167654184 | G | T | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+23755G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654184 | |||||||
chr1:167654226 | G | T | 3 | a0001c0003t0026g0218 a0002c0002t0009g0212 a0002c0002t0009g0269 |
3 | HG01109.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6+23797G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654226 | |||||||
chr1:167654376 | A | G | 8 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+23947A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654376 | |||||||
chr1:167654547 | T | C | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+24118T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654547 | |||||||
chr1:167654775 | C | T | 8 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+24346C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167654775 | |||||||
chr1:167655113 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0045g0109 |
2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+24684C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655113 | |||||||
chr1:167655114 | G | T | 16 | a0001c0001t0001g0152 a0001c0001t0001g0272 a0001c0001t0002g0141 others(13): Show |
16 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.6+24685G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655114 | |||||||
chr1:167655240 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0045g0109 |
2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6+24811G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655240 | |||||||
chr1:167655327 | C | T | 2 | a0001c0001t0004g0091 a0001c0001t0010g0073 |
2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6+24898C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655327 | |||||||
chr1:167655362 | AT | A | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+24940delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167655362 | ||||||
chr1:167655533 | C | T | 4 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+25104C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655533 | |||||||
chr1:167655534 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6+25105G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655534 | |||||||
chr1:167655555 | C | A | 8 | a0001c0001t0001g0287 a0001c0001t0001g0289 a0001c0001t0005g0288 others(5): Show |
8 | HG01169.hp2 HG01496.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+25126C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655555 | |||||||
chr1:167655818 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0139 others(16): Show |
19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6+25389G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167655818 | |||||||
chr1:167656101 | A | G | 2 | a0001c0001t0006g0225 a0001c0001t0006g0226 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6+25672A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656101 | |||||||
chr1:167656134 | T | G | 1 | a0001c0001t0005g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6+25705T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656134 | |||||||
chr1:167656177 | A | G | 1 | a0001c0001t0039g0337 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6+25748A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656177 | |||||||
chr1:167656207 | G | A | 1 | a0001c0001t0037g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6+25778G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656207 | |||||||
chr1:167656208 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+25779C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656208 | |||||||
chr1:167656258 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0139 others(16): Show |
19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6+25829A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656258 | |||||||
chr1:167656328 | G | A | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6+25899G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656328 | |||||||
chr1:167656415 | C | T | 72 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(69): Show |
72 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.6+25986C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656415 | |||||||
chr1:167656595 | C | G | 1 | a0001c0001t0001g0333 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6+26166C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656595 | |||||||
chr1:167656659 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0023g0227 a0001c0010t0001g0012 |
3 | HG01169.hp2 HG01496.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6+26230G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656659 | |||||||
chr1:167656851 | A | G | 1 | a0001c0001t0003g0256 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.6+26422A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656851 | |||||||
chr1:167656993 | C | T | 2 | a0001c0001t0009g0334 a0001c0001t0015g0239 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6+26564C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167656993 | |||||||
chr1:167657077 | A | C | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+26648A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657077 | |||||||
chr1:167657466 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.7-26434A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657466 | |||||||
chr1:167657548 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-26352G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657548 | |||||||
chr1:167657588 | T | C | 22 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0137 others(19): Show |
22 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-26312T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657588 | |||||||
chr1:167657694 | G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7-26206G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657694 | |||||||
chr1:167657780 | A | T | 7 | a0001c0001t0002g0149 a0001c0001t0002g0178 a0001c0001t0002g0197 others(4): Show |
7 | HG00609.hp2 HG00621.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-26120A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657780 | |||||||
chr1:167657854 | G | A | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-26046G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167657854 | |||||||
chr1:167657891 | G | GCA | 7 | a0001c0001t0001g0131 a0001c0001t0001g0222 a0001c0001t0002g0040 others(4): Show |
7 | HG01074.hp2 HG01515.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-25986_7-25985dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | ||||||
chr1:167657891 | GCA | G | 28 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0139 others(25): Show |
28 | HG00280.hp1 HG01169.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.7-25986_7-25985del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | ||||||
chr1:167657891 | GCACA | G | 5 | a0001c0001t0001g0324 a0001c0001t0008g0329 a0001c0001t0008g0331 others(2): Show |
5 | HG01891.hp1 HG02165.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-25988_7-25985del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167657891 | ||||||
chr1:167658031 | G | A | 3 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7-25869G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658031 | |||||||
chr1:167658062 | G | C | 1 | a0001c0005t0008g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7-25838G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658062 | |||||||
chr1:167658235 | A | T | 3 | a0001c0001t0001g0328 a0001c0001t0005g0237 a0001c0001t0041g0311 |
3 | HG02109.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7-25665A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658235 | |||||||
chr1:167658242 | A | T | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-25658A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658242 | |||||||
chr1:167658416 | G | T | 2 | a0001c0001t0001g0139 a0001c0001t0045g0109 |
2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.7-25484G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658416 | |||||||
chr1:167658471 | A | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0137 others(19): Show |
22 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-25429A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658471 | |||||||
chr1:167658528 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0045g0109 |
2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.7-25372C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658528 | |||||||
chr1:167658556 | A | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0137 others(19): Show |
22 | HG01169.hp2 HG01496.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-25344A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658556 | |||||||
chr1:167658582 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0328 others(4): Show |
7 | HG00280.hp1 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-25318C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658582 | |||||||
chr1:167658602 | T | C | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-25298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658602 | |||||||
chr1:167658603 | C | T | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-25297C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658603 | |||||||
chr1:167658615 | G | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0139 others(16): Show |
19 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-25285G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658615 | |||||||
chr1:167658619 | C | T | 4 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-25281C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658619 | |||||||
chr1:167658729 | C | A | 1 | a0001c0001t0011g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.7-25171C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658729 | |||||||
chr1:167658943 | T | G | 3 | a0001c0001t0001g0238 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7-24957T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658943 | |||||||
chr1:167658998 | C | A | 5 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0001t0008g0310 others(2): Show |
5 | HG02559.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-24902C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167658998 | |||||||
chr1:167659054 | C | T | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-24846C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659054 | |||||||
chr1:167659163 | C | A | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-24737C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659163 | |||||||
chr1:167659222 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-24678G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659222 | |||||||
chr1:167659366 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0034g0183 |
2 | HG01070.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7-24534T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659366 | |||||||
chr1:167659554 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-24346C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659554 | |||||||
chr1:167659638 | G | A | 4 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0017g0341 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-24262G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659638 | |||||||
chr1:167659713 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-24187A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659713 | |||||||
chr1:167659727 | T | G | 1 | a0001c0001t0004g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.7-24173T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659727 | |||||||
chr1:167659858 | C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7-24042C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659858 | |||||||
chr1:167659880 | G | A | 1 | a0001c0001t0028g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7-24020G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167659880 | |||||||
chr1:167660007 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7-23893G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660007 | |||||||
chr1:167660122 | C | T | 15 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0287 others(12): Show |
15 | HG00280.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-23778C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660122 | |||||||
chr1:167660248 | G | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0287 others(12): Show |
15 | HG00280.hp1 HG01081.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-23652G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660248 | |||||||
chr1:167660254 | C | T | 4 | a0001c0001t0001g0287 a0001c0001t0022g0342 a0001c0001t0023g0227 others(1): Show |
4 | HG01169.hp2 HG01496.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-23646C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660254 | |||||||
chr1:167660305 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7-23595G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660305 | |||||||
chr1:167660432 | G | C | 37 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(34): Show |
37 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-23468G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660432 | |||||||
chr1:167660471 | T | TTG | 7 | a0001c0001t0003g0004 a0001c0001t0003g0236 a0001c0001t0005g0243 others(4): Show |
7 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-23428_7-23427ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167660471 | ||||||
chr1:167660472 | T | TG | 19 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0107 others(16): Show |
19 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-23428_7-23427ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660472 | |||||||
chr1:167660473 | T | G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0328 others(8): Show |
11 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.7-23427T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660473 | |||||||
chr1:167660475 | G | GT | 6 | a0001c0001t0001g0139 a0001c0001t0017g0338 a0001c0001t0018g0339 others(3): Show |
6 | HG00280.hp1 HG01081.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-23412dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167660475 | ||||||
chr1:167660475 | G | T | 26 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0107 others(23): Show |
26 | HG01934.hp2 HG01981.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.7-23425G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660475 | |||||||
chr1:167660480 | T | G | 2 | a0001c0001t0012g0251 a0001c0001t0012g0312 |
2 | NA18984.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.7-23420T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660480 | |||||||
chr1:167660608 | G | T | 4 | a0001c0001t0017g0338 a0001c0001t0018g0339 a0001c0001t0018g0340 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-23292G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660608 | |||||||
chr1:167660691 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0023g0227 a0001c0010t0001g0012 |
3 | HG01169.hp2 HG01496.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7-23209C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167660691 | |||||||
chr1:167661076 | C | T | 36 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0033 others(33): Show |
36 | HG01081.hp2 HG01884.hp2 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-22824C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661076 | |||||||
chr1:167661197 | T | C | 9 | a0001c0001t0001g0328 a0001c0001t0005g0237 a0001c0001t0017g0338 others(6): Show |
9 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-22703T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661197 | |||||||
chr1:167661276 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-22624C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661276 | |||||||
chr1:167661615 | G | C | 1 | a0001c0001t0001g0333 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.7-22285G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661615 | |||||||
chr1:167661688 | C | T | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7-22212C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661688 | |||||||
chr1:167661754 | T | A | 5 | a0001c0001t0001g0033 a0001c0001t0005g0237 a0001c0001t0016g0327 others(2): Show |
5 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-22146T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661754 | |||||||
chr1:167661908 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7-21992A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661908 | |||||||
chr1:167661949 | G | C | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-21951G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661949 | |||||||
chr1:167661997 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-21903G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167661997 | |||||||
chr1:167662070 | G | A | 28 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(25): Show |
28 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.7-21830G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662070 | |||||||
chr1:167662112 | T | C | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-21788T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662112 | |||||||
chr1:167662427 | G | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(27): Show |
30 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-21473G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662427 | |||||||
chr1:167662569 | C | T | 20 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-21331C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662569 | |||||||
chr1:167662677 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-21223T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662677 | |||||||
chr1:167662760 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7-21140T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662760 | |||||||
chr1:167662796 | C | T | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-21104C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662796 | |||||||
chr1:167662800 | C | G | 5 | a0001c0001t0001g0033 a0001c0001t0005g0237 a0001c0001t0016g0327 others(2): Show |
5 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-21100C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662800 | |||||||
chr1:167662800 | C | T | 66 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(63): Show |
66 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.7-21100C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662800 | |||||||
chr1:167662801 | G | A | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-21099G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662801 | |||||||
chr1:167662810 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7-21090G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662810 | |||||||
chr1:167662845 | G | C | 36 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0103 others(33): Show |
36 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-21055G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662845 | |||||||
chr1:167662864 | T | A | 36 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0103 others(33): Show |
36 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-21036T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662864 | |||||||
chr1:167662974 | T | A | 4 | a0001c0001t0005g0326 a0001c0001t0020g0301 a0001c0001t0021g0005 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-20926T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167662974 | |||||||
chr1:167663034 | A | G | 69 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-20866A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663034 | |||||||
chr1:167663124 | G | T | 30 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(27): Show |
30 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-20776G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663124 | |||||||
chr1:167663179 | G | A | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7-20721G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663179 | |||||||
chr1:167663239 | G | C | 2 | a0001c0001t0001g0252 a0004c0006t0002g0207 |
2 | HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.7-20661G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663239 | |||||||
chr1:167663242 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7-20658G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663242 | |||||||
chr1:167663381 | G | A | 69 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-20519G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663381 | |||||||
chr1:167663408 | CG | C | 69 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-20490delG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167663408 | ||||||
chr1:167663409 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-20491G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663409 | |||||||
chr1:167663417 | C | A | 4 | a0001c0001t0005g0326 a0001c0001t0020g0301 a0001c0001t0021g0005 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-20483C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663417 | |||||||
chr1:167663451 | C | T | 23 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(20): Show |
23 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-20449C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663451 | |||||||
chr1:167663539 | A | T | 69 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-20361A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663539 | |||||||
chr1:167663585 | T | C | 69 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-20315T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663585 | |||||||
chr1:167663620 | C | T | 1 | a0001c0001t0022g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7-20280C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663620 | |||||||
chr1:167663621 | G | A | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-20279G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663621 | |||||||
chr1:167663811 | T | C | 2 | a0001c0001t0012g0251 a0001c0001t0012g0312 |
2 | NA18984.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.7-20089T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663811 | |||||||
chr1:167663827 | C | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0231 a0001c0001t0017g0338 others(3): Show |
6 | HG00280.hp1 HG01884.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-20073C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663827 | |||||||
chr1:167663942 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0004g0088 |
2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.7-19958A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167663942 | |||||||
chr1:167664033 | G | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0231 a0001c0001t0017g0338 others(3): Show |
6 | HG00280.hp1 HG01884.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-19867G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664033 | |||||||
chr1:167664355 | G | C | 7 | a0001c0001t0001g0107 a0001c0001t0002g0170 a0001c0001t0002g0195 others(4): Show |
7 | NA18954.hp2 NA18983.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-19545G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664355 | |||||||
chr1:167664359 | C | A | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-19541C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664359 | |||||||
chr1:167664365 | G | A | 1 | a0001c0001t0004g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7-19535G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664365 | |||||||
chr1:167664595 | G | A | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7-19305G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664595 | |||||||
chr1:167664606 | A | C | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-19294A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664606 | |||||||
chr1:167664624 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0023g0227 a0001c0010t0001g0012 |
3 | HG01496.hp1 HG03453.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.7-19276G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664624 | |||||||
chr1:167664740 | A | G | 4 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0001t0009g0290 others(1): Show |
4 | HG02559.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-19160A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664740 | |||||||
chr1:167664808 | G | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0208 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.7-19092G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664808 | |||||||
chr1:167664830 | A | G | 71 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.7-19070A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664830 | |||||||
chr1:167664835 | T | G | 1 | a0001c0001t0010g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.7-19065T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664835 | |||||||
chr1:167664881 | A | C | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-19019A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664881 | |||||||
chr1:167664993 | G | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0038 others(32): Show |
35 | HG00558.hp1 HG01081.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.7-18907G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167664993 | |||||||
chr1:167665040 | C | CAA | 23 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0038 others(20): Show |
23 | HG01070.hp2 HG01081.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-18844_7-18843dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665040 | ||||||
chr1:167665055 | A | AAG | 14 | a0001c0001t0001g0137 a0001c0001t0001g0275 a0001c0001t0001g0289 others(11): Show |
14 | HG00558.hp1 HG01891.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-18844_7-18843ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665055 | ||||||
chr1:167665055 | A | AG | 8 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-18845_7-18844ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665055 | |||||||
chr1:167665055 | A | G | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-18845A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665055 | |||||||
chr1:167665335 | G | A | 35 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0103 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.7-18565G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665335 | |||||||
chr1:167665347 | TTGTC | T | 23 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(20): Show |
23 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-18547_7-18544del others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665347 | ||||||
chr1:167665408 | A | G | 6 | a0001c0001t0001g0059 a0001c0001t0005g0326 a0001c0001t0020g0301 others(3): Show |
6 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-18492A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665408 | |||||||
chr1:167665481 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-18419A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665481 | |||||||
chr1:167665488 | T | C | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7-18412T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665488 | |||||||
chr1:167665498 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-18402G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665498 | |||||||
chr1:167665635 | A | G | 7 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0001t0008g0329 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-18265A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665635 | |||||||
chr1:167665668 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-18232G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665668 | |||||||
chr1:167665817 | C | CT | 30 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(27): Show |
30 | HG00558.hp1 HG01070.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-18071dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167665817 | ||||||
chr1:167665857 | T | A | 3 | a0001c0001t0002g0170 a0001c0001t0003g0230 a0001c0001t0003g0255 |
3 | NA19011.hp1 NA19056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.7-18043T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665857 | |||||||
chr1:167665867 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7-18033G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665867 | |||||||
chr1:167665881 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-18019C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665881 | |||||||
chr1:167665894 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.7-18006C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665894 | |||||||
chr1:167665950 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0289 a0001c0001t0005g0288 others(5): Show |
8 | HG01496.hp1 HG02559.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-17950T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665950 | |||||||
chr1:167665957 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0003g0004 a0001c0001t0003g0236 others(6): Show |
9 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-17943G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665957 | |||||||
chr1:167665973 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0129 |
3 | HG00642.hp1 NA19000.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.7-17927G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665973 | |||||||
chr1:167665977 | A | T | 1 | a0001c0001t0005g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7-17923A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167665977 | |||||||
chr1:167666014 | G | A | 2 | a0001c0001t0004g0091 a0001c0001t0010g0073 |
2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7-17886G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666014 | |||||||
chr1:167666094 | A | G | 90 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.7-17806A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666094 | |||||||
chr1:167666267 | T | C | 2 | a0001c0001t0001g0059 a0001c0010t0001g0012 |
2 | HG01496.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.7-17633T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666267 | |||||||
chr1:167666320 | C | T | 2 | a0001c0001t0004g0126 a0001c0001t0010g0248 |
2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.7-17580C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666320 | |||||||
chr1:167666338 | A | G | 90 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.7-17562A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666338 | |||||||
chr1:167666508 | G | C | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-17392G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666508 | |||||||
chr1:167666534 | A | G | 9 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-17366A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666534 | |||||||
chr1:167666585 | C | T | 5 | a0001c0001t0005g0326 a0001c0001t0017g0341 a0001c0001t0020g0301 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-17315C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666585 | |||||||
chr1:167666592 | C | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0293 a0001c0001t0036g0280 |
3 | NA18947.hp2 NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.7-17308C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666592 | |||||||
chr1:167666727 | C | T | 3 | a0001c0001t0008g0329 a0001c0001t0008g0331 a0001c0001t0018g0330 |
3 | HG01891.hp1 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-17173C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666727 | |||||||
chr1:167666879 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-17021A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167666879 | |||||||
chr1:167667103 | C | CCATTGTA others(31): Show |
3 | a0001c0001t0003g0306 a0001c0001t0044g0217 a0001c0001t0053g0096 |
3 | HG01891.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7-16763_7-16726dup others(38): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167667103 | ||||||
chr1:167667103 | CCATTGTA others(31): Show |
C | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-16763_7-16726del others(38): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167667103 | ||||||
chr1:167667210 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.7-16690T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667210 | |||||||
chr1:167667323 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0221 a0001c0001t0005g0237 others(5): Show |
8 | HG02109.hp1 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-16577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667323 | |||||||
chr1:167667324 | G | A | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-16576G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667324 | |||||||
chr1:167667383 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-16517A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667383 | |||||||
chr1:167667422 | A | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0046 others(43): Show |
47 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.7-16478A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667422 | |||||||
chr1:167667423 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.7-16477A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667423 | |||||||
chr1:167667470 | A | T | 1 | a0001c0001t0001g0308 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-16430A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667470 | |||||||
chr1:167667577 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-16323T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667577 | |||||||
chr1:167667769 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0046 others(40): Show |
44 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.7-16131A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667769 | |||||||
chr1:167667813 | A | G | 4 | a0001c0001t0001g0328 a0001c0001t0017g0338 a0001c0001t0018g0339 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-16087A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667813 | |||||||
chr1:167667835 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.7-16065T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167667835 | |||||||
chr1:167668018 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.7-15882T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668018 | |||||||
chr1:167668083 | G | C | 1 | a0001c0001t0028g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7-15817G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668083 | |||||||
chr1:167668120 | C | T | 2 | a0001c0001t0001g0336 a0001c0001t0023g0227 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.7-15780C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668120 | |||||||
chr1:167668178 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7-15722G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668178 | |||||||
chr1:167668178 | G | T | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7-15722G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668178 | |||||||
chr1:167668287 | G | A | 20 | a0001c0001t0001g0033 a0001c0001t0001g0221 a0001c0001t0001g0328 others(17): Show |
20 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.7-15613G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668287 | |||||||
chr1:167668396 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.7-15504G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668396 | |||||||
chr1:167668487 | A | T | 9 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-15413A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668487 | |||||||
chr1:167668526 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.7-15374A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668526 | |||||||
chr1:167668530 | C | A | 5 | a0001c0001t0001g0320 a0001c0001t0003g0321 a0001c0001t0003g0322 others(2): Show |
5 | HG02040.hp2 NA18971.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-15370C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668530 | |||||||
chr1:167668705 | T | TAATG | 4 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0010g0249 others(1): Show |
4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-15183_7-15180dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668705 | ||||||
chr1:167668731 | T | C | 4 | a0001c0001t0005g0237 a0001c0001t0008g0310 a0001c0001t0016g0327 others(1): Show |
4 | HG02109.hp1 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-15169T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668731 | |||||||
chr1:167668736 | TA | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.7-15147delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668736 | ||||||
chr1:167668736 | TAAA | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
20 | HG00408.hp2 HG00558.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-15149_7-15147del others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167668736 | ||||||
chr1:167668816 | G | A | 1 | a0001c0001t0001g0347 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7-15084G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668816 | |||||||
chr1:167668887 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(170): Show |
175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.7-15013G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668887 | |||||||
chr1:167668966 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.7-14934T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167668966 | |||||||
chr1:167669014 | T | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.7-14886T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669014 | |||||||
chr1:167669051 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0048 others(22): Show |
26 | HG00438.hp2 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.7-14849T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669051 | |||||||
chr1:167669186 | C | T | 18 | a0001c0001t0001g0033 a0001c0001t0001g0221 a0001c0001t0003g0236 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.7-14714C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669186 | |||||||
chr1:167669202 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-14698A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669202 | |||||||
chr1:167669214 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(170): Show |
175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.7-14686C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669214 | |||||||
chr1:167669224 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(157): Show |
162 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.7-14676T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669224 | |||||||
chr1:167669320 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(163): Show |
168 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.7-14580G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669320 | |||||||
chr1:167669380 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7-14520G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669380 | |||||||
chr1:167669454 | G | C | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-14446G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669454 | |||||||
chr1:167669779 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0188 a0001c0001t0012g0008 |
3 | HG00558.hp2 NA18960.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.7-14121A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669779 | |||||||
chr1:167669833 | G | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(103): Show |
107 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-14067G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669833 | |||||||
chr1:167669902 | T | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(103): Show |
107 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-13998T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669902 | |||||||
chr1:167669987 | ACACACG | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.7-13901_7-13896del others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167669987 | ||||||
chr1:167669999 | G | T | 2 | a0001c0001t0001g0025 a0001c0001t0002g0143 |
2 | NA18990.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.7-13901G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167669999 | |||||||
chr1:167670072 | C | T | 7 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0001t0017g0338 others(4): Show |
7 | HG01884.hp2 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-13828C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670072 | |||||||
chr1:167670094 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0319 a0001c0001t0020g0301 others(4): Show |
8 | HG01243.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-13806C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670094 | |||||||
chr1:167670160 | C | G | 8 | a0001c0001t0001g0238 a0001c0001t0006g0225 a0001c0001t0006g0226 others(5): Show |
8 | HG02717.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-13740C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670160 | |||||||
chr1:167670261 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 |
3 | HG02630.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7-13639G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670261 | |||||||
chr1:167670327 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7-13573A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670327 | |||||||
chr1:167670357 | G | GA | 22 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0001g0221 others(19): Show |
22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-13527dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | ||||||
chr1:167670357 | G | GAA | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.7-13528_7-13527dup others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | ||||||
chr1:167670357 | G | GAAA | 70 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0048 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.7-13529_7-13527dup others(3): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | ||||||
chr1:167670357 | G | GAAAA | 6 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0139 others(3): Show |
6 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-13530_7-13527dup others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167670357 | ||||||
chr1:167670422 | C | T | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7-13478C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670422 | |||||||
chr1:167670549 | C | T | 3 | a0001c0001t0001g0328 a0001c0001t0008g0310 a0001c0001t0016g0327 |
3 | HG02486.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7-13351C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670549 | |||||||
chr1:167670618 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.7-13282C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670618 | |||||||
chr1:167670719 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7-13181C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670719 | |||||||
chr1:167670737 | C | G | 4 | a0001c0001t0005g0326 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-13163C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670737 | |||||||
chr1:167670738 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7-13162C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670738 | |||||||
chr1:167670783 | A | C | 36 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0101 others(33): Show |
36 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-13117A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670783 | |||||||
chr1:167670885 | C | T | 37 | a0001c0001t0001g0046 a0001c0001t0001g0070 a0001c0001t0001g0101 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.7-13015C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670885 | |||||||
chr1:167670949 | C | T | 1 | a0001c0001t0009g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-12951C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670949 | |||||||
chr1:167670996 | C | T | 41 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0038 others(38): Show |
41 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.7-12904C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167670996 | |||||||
chr1:167671076 | G | A | 5 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0003g0286 others(2): Show |
5 | HG00099.hp2 HG01515.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-12824G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671076 | |||||||
chr1:167671375 | T | C | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7-12525T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671375 | |||||||
chr1:167671407 | G | A | 2 | a0001c0001t0004g0072 a0001c0001t0004g0092 |
2 | NA18942.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.7-12493G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671407 | |||||||
chr1:167671433 | C | T | 1 | a0001c0001t0023g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7-12467C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671433 | |||||||
chr1:167671474 | T | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.7-12426T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671474 | |||||||
chr1:167671590 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.7-12310A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671590 | |||||||
chr1:167671602 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.7-12298T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671602 | |||||||
chr1:167671881 | C | T | 3 | a0001c0003t0026g0218 a0002c0002t0009g0212 a0002c0002t0009g0269 |
3 | HG01109.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7-12019C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671881 | |||||||
chr1:167671917 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7-11983G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167671917 | |||||||
chr1:167672042 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0004g0127 |
3 | HG00323.hp1 HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.7-11858A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672042 | |||||||
chr1:167672055 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.7-11845A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672055 | |||||||
chr1:167672132 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0017g0341 a0001c0001t0022g0241 others(2): Show |
5 | HG02818.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-11768G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672132 | |||||||
chr1:167672142 | A | G | 6 | a0001c0001t0001g0070 a0001c0001t0001g0139 a0001c0001t0002g0151 others(3): Show |
6 | HG00280.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-11758A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672142 | |||||||
chr1:167672174 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0005t0008g0296 |
3 | HG02559.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7-11726C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672174 | |||||||
chr1:167672541 | T | C | 27 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0101 others(24): Show |
27 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.7-11359T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672541 | |||||||
chr1:167672707 | C | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.7-11193C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672707 | |||||||
chr1:167672786 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0017g0341 a0001c0001t0022g0241 others(2): Show |
5 | HG02818.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-11114A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672786 | |||||||
chr1:167672873 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.7-11027A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672873 | |||||||
chr1:167672884 | T | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0139 a0001c0001t0002g0151 others(3): Show |
6 | HG00280.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-11016T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672884 | |||||||
chr1:167672889 | C | T | 3 | a0001c0001t0001g0328 a0001c0001t0003g0004 a0001c0001t0016g0327 |
3 | HG02486.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7-11011C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672889 | |||||||
chr1:167672951 | C | T | 1 | a0001c0001t0023g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7-10949C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672951 | |||||||
chr1:167672959 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0005g0288 a0001c0005t0008g0296 |
3 | HG02559.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7-10941C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167672959 | |||||||
chr1:167673080 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.7-10820G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673080 | |||||||
chr1:167673094 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7-10806G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673094 | |||||||
chr1:167673200 | G | C | 24 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0064 others(21): Show |
24 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-10700G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673200 | |||||||
chr1:167673257 | T | C | 85 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0044 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.7-10643T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673257 | |||||||
chr1:167673288 | T | C | 3 | a0001c0001t0003g0306 a0001c0001t0044g0217 a0001c0001t0053g0096 |
3 | HG01891.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7-10612T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673288 | |||||||
chr1:167673330 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.7-10570C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673330 | |||||||
chr1:167673483 | G | A | 1 | a0001c0001t0019g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7-10417G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673483 | |||||||
chr1:167673527 | T | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-10373T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673527 | |||||||
chr1:167673570 | C | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.7-10330C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673570 | |||||||
chr1:167673629 | A | T | 1 | a0001c0001t0004g0247 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7-10271A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673629 | |||||||
chr1:167673699 | C | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0016 others(35): Show |
39 | HG00323.hp1 HG00609.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.7-10201C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673699 | |||||||
chr1:167673755 | C | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0044 others(34): Show |
37 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-10145C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673755 | |||||||
chr1:167673800 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.7-10100C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673800 | |||||||
chr1:167673805 | G | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0276 a0001c0001t0003g0130 others(1): Show |
4 | NA18952.hp1 NA18960.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-10095G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673805 | |||||||
chr1:167673892 | A | G | 256 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.7-10008A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673892 | |||||||
chr1:167673941 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7-9959T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673941 | |||||||
chr1:167673947 | T | C | 14 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0254 others(11): Show |
14 | HG00099.hp1 HG00280.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-9953T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673947 | |||||||
chr1:167673981 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0054 others(40): Show |
44 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.7-9919C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167673981 | |||||||
chr1:167674003 | T | C | 2 | a0001c0001t0010g0077 a0001c0001t0049g0211 |
2 | NA18961.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.7-9897T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674003 | |||||||
chr1:167674044 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.7-9856G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674044 | |||||||
chr1:167674118 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0045g0109 |
2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.7-9782A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674118 | |||||||
chr1:167674176 | G | C | 198 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0021 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.7-9724G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674176 | |||||||
chr1:167674224 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0038 others(63): Show |
67 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.7-9676C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674224 | |||||||
chr1:167674227 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0002g0206 a0001c0001t0005g0237 others(2): Show |
5 | HG01070.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-9673G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674227 | |||||||
chr1:167674249 | C | G | 6 | a0001c0001t0008g0219 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-9651C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674249 | |||||||
chr1:167674444 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0270 others(36): Show |
40 | HG01081.hp2 HG01175.hp2 HG02074.hp2 others(37): Show |
intron_variant | MODIFIER | c.7-9456C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674444 | |||||||
chr1:167674455 | TA | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0270 others(32): Show |
36 | HG01081.hp2 HG01175.hp2 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.7-9440delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167674455 | ||||||
chr1:167674482 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-9418G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674482 | |||||||
chr1:167674559 | A | G | 7 | a0001c0001t0001g0261 a0001c0001t0001g0270 a0001c0001t0009g0128 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-9341A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674559 | |||||||
chr1:167674620 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7-9280C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674620 | |||||||
chr1:167674779 | A | G | 19 | a0001c0001t0001g0038 a0001c0001t0001g0221 a0001c0001t0001g0238 others(16): Show |
19 | HG01070.hp1 HG01109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-9121A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674779 | |||||||
chr1:167674928 | C | T | 4 | a0001c0001t0002g0166 a0001c0001t0004g0056 a0001c0001t0014g0177 others(1): Show |
4 | HG02027.hp2 NA18979.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-8972C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674928 | |||||||
chr1:167674932 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7-8968T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674932 | |||||||
chr1:167674934 | C | T | 5 | a0001c0001t0002g0166 a0001c0001t0004g0056 a0001c0001t0014g0177 others(2): Show |
5 | HG02027.hp2 HG02486.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8966C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674934 | |||||||
chr1:167674935 | G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7-8965G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674935 | |||||||
chr1:167674940 | C | T | 139 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.7-8960C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674940 | |||||||
chr1:167674981 | T | C | 8 | a0001c0001t0003g0004 a0001c0001t0008g0219 a0001c0001t0015g0052 others(5): Show |
8 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-8919T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674981 | |||||||
chr1:167674983 | A | G | 7 | a0001c0001t0003g0004 a0001c0001t0008g0219 a0001c0001t0015g0052 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8917A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674983 | |||||||
chr1:167674989 | A | G | 7 | a0001c0001t0003g0004 a0001c0001t0008g0219 a0001c0001t0015g0052 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8911A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674989 | |||||||
chr1:167674991 | A | G | 7 | a0001c0001t0003g0004 a0001c0001t0008g0219 a0001c0001t0015g0052 others(4): Show |
7 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8909A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167674991 | |||||||
chr1:167675000 | A | T | 1 | a0001c0001t0024g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7-8900A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675000 | |||||||
chr1:167675002 | C | G | 5 | a0001c0001t0001g0238 a0001c0001t0017g0338 a0001c0001t0017g0341 others(2): Show |
5 | HG01109.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-8898C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675002 | |||||||
chr1:167675003 | A | G | 110 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.7-8897A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675003 | |||||||
chr1:167675018 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0266 a0001c0001t0003g0134 |
3 | HG03942.hp1 NA18957.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.7-8882A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675018 | |||||||
chr1:167675023 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7-8877A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675023 | |||||||
chr1:167675030 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7-8870C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675030 | |||||||
chr1:167675099 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0105 others(35): Show |
39 | HG00438.hp1 HG01070.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.7-8801C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675099 | |||||||
chr1:167675119 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0101 others(63): Show |
67 | HG00099.hp2 HG00438.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.7-8781C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675119 | |||||||
chr1:167675207 | G | GA | 74 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0038 others(71): Show |
74 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.7-8668dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | ||||||
chr1:167675207 | G | GAA | 9 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0005g0111 others(6): Show |
9 | HG00621.hp1 HG00741.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-8669_7-8668dupAA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | ||||||
chr1:167675207 | G | GGA | 6 | a0001c0001t0001g0328 a0001c0001t0022g0342 a0001c0001t0028g0335 others(3): Show |
6 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | |||||||
chr1:167675207 | G | GGAA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0281 a0001c0001t0001g0289 others(9): Show |
13 | HG02109.hp2 HG02723.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | |||||||
chr1:167675207 | G | GGAAA | 6 | a0001c0001t0001g0279 a0001c0001t0003g0004 a0001c0001t0005g0326 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-8693_7-8692insGA others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675207 | |||||||
chr1:167675207 | GA | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0049 others(28): Show |
31 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.7-8668delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167675207 | ||||||
chr1:167675356 | G | A | 2 | a0001c0001t0001g0252 a0004c0006t0002g0207 |
2 | HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.7-8544G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675356 | |||||||
chr1:167675358 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0105 others(21): Show |
25 | HG00438.hp1 HG01081.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.7-8542G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675358 | |||||||
chr1:167675430 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0221 others(46): Show |
50 | HG01074.hp2 HG01081.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.7-8470C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675430 | |||||||
chr1:167675487 | C | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-8413C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675487 | |||||||
chr1:167675493 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0101 others(42): Show |
46 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-8407T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675493 | |||||||
chr1:167675512 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0101 others(42): Show |
46 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-8388T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675512 | |||||||
chr1:167675639 | C | T | 5 | a0001c0001t0005g0243 a0001c0001t0018g0330 a0001c0001t0018g0339 others(2): Show |
5 | HG01884.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8261C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675639 | |||||||
chr1:167675651 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0022 |
2 | NA18950.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.7-8249C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675651 | |||||||
chr1:167675674 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0005g0237 a0001c0001t0023g0227 others(2): Show |
5 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-8226G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675674 | |||||||
chr1:167675855 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-8045C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167675855 | |||||||
chr1:167676429 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-7471A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676429 | |||||||
chr1:167676491 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.7-7409T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676491 | |||||||
chr1:167676638 | G | C | 1 | a0001c0001t0032g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.7-7262G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676638 | |||||||
chr1:167676736 | C | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(27): Show |
31 | HG00280.hp2 HG00741.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-7164C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676736 | |||||||
chr1:167676866 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-7034G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676866 | |||||||
chr1:167676871 | A | G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0010g0249 others(1): Show |
4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-7029A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676871 | |||||||
chr1:167676880 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7-7020T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676880 | |||||||
chr1:167676969 | A | T | 1 | a0001c0001t0003g0006 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7-6931A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676969 | |||||||
chr1:167676985 | C | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(27): Show |
31 | HG00280.hp2 HG00741.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-6915C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167676985 | |||||||
chr1:167677194 | GA | G | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-6701delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167677194 | ||||||
chr1:167677222 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-6678G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677222 | |||||||
chr1:167677226 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7-6674C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677226 | |||||||
chr1:167677237 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(20): Show |
23 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-6663A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677237 | |||||||
chr1:167677337 | T | C | 1 | a0001c0001t0050g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7-6563T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677337 | |||||||
chr1:167677477 | G | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(26): Show |
30 | HG00741.hp1 HG01433.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.7-6423G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677477 | |||||||
chr1:167677774 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.7-6126C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677774 | |||||||
chr1:167677935 | G | T | 5 | a0001c0001t0015g0052 a0001c0001t0015g0239 a0001c0001t0015g0304 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-5965G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677935 | |||||||
chr1:167677957 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0059 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.7-5943G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677957 | |||||||
chr1:167677971 | C | A | 10 | a0001c0001t0001g0013 a0001c0001t0011g0042 a0001c0001t0011g0043 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-5929C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167677971 | |||||||
chr1:167678158 | T | C | 4 | a0001c0001t0005g0237 a0001c0001t0023g0227 a0001c0001t0023g0259 others(1): Show |
4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5742T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678158 | |||||||
chr1:167678262 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-5638A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678262 | |||||||
chr1:167678323 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7-5577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678323 | |||||||
chr1:167678324 | G | A | 4 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0010g0249 others(1): Show |
4 | NA18970.hp1 NA18972.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5576G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678324 | |||||||
chr1:167678336 | T | G | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7-5564T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678336 | |||||||
chr1:167678402 | CCAACATG others(5): Show |
C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(13): Show |
17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7-5493_7-5482delAT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167678402 | ||||||
chr1:167678573 | C | T | 4 | a0001c0001t0005g0243 a0001c0001t0018g0330 a0001c0001t0018g0339 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5327C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678573 | |||||||
chr1:167678606 | C | A | 1 | a0002c0002t0009g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7-5294C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678606 | |||||||
chr1:167678695 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-5205T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678695 | |||||||
chr1:167678738 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(13): Show |
17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7-5162C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678738 | |||||||
chr1:167678785 | G | T | 3 | a0001c0001t0027g0078 a0001c0001t0027g0089 a0001c0001t0043g0015 |
3 | NA18947.hp1 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.7-5115G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678785 | |||||||
chr1:167678797 | C | A | 2 | a0001c0001t0009g0213 a0001c0001t0052g0158 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7-5103C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678797 | |||||||
chr1:167678861 | C | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-5039C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678861 | |||||||
chr1:167678911 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-4989C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167678911 | |||||||
chr1:167679011 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-4889G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679011 | |||||||
chr1:167679156 | A | G | 14 | a0001c0001t0001g0328 a0001c0001t0003g0004 a0001c0001t0009g0128 others(11): Show |
14 | HG01081.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-4744A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679156 | |||||||
chr1:167679232 | CT | C | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-4666delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167679232 | ||||||
chr1:167679316 | C | G | 1 | a0001c0001t0017g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7-4584C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679316 | |||||||
chr1:167679403 | T | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
21 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-4497T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679403 | |||||||
chr1:167679410 | C | A | 1 | a0001c0001t0004g0246 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7-4490C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679410 | |||||||
chr1:167679528 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7-4372G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679528 | |||||||
chr1:167679567 | G | T | 1 | a0001c0001t0007g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-4333G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679567 | |||||||
chr1:167679632 | G | A | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.7-4268G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679632 | |||||||
chr1:167679674 | C | T | 1 | a0001c0001t0050g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7-4226C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679674 | |||||||
chr1:167679827 | G | T | 1 | a0001c0001t0003g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7-4073G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679827 | |||||||
chr1:167679921 | A | G | 1 | a0001c0001t0019g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.7-3979A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167679921 | |||||||
chr1:167680060 | T | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-3840T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680060 | |||||||
chr1:167680098 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-3802G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680098 | |||||||
chr1:167680409 | G | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0197 a0001c0001t0004g0124 |
3 | HG00673.hp2 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.7-3491G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680409 | |||||||
chr1:167680448 | C | CTGTTTT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
50 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-3414_7-3409dupGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | ||||||
chr1:167680448 | C | CTGTTTTT others(5): Show |
4 | a0001c0001t0001g0187 a0001c0001t0006g0223 a0001c0001t0006g0257 others(1): Show |
4 | HG00741.hp1 HG01433.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-3420_7-3409dupGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | ||||||
chr1:167680448 | C | CTGTTTTT others(11): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0064 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7-3426_7-3409dupGT others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | ||||||
chr1:167680448 | CTGTTTT | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0221 a0001c0001t0001g0282 others(21): Show |
24 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-3414_7-3409delGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | ||||||
chr1:167680448 | CTGTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(6): Show |
10 | HG00423.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-3420_7-3409delGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167680448 | ||||||
chr1:167680566 | G | A | 14 | a0001c0001t0001g0328 a0001c0001t0003g0004 a0001c0001t0009g0128 others(11): Show |
14 | HG01081.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-3334G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680566 | |||||||
chr1:167680629 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7-3271C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680629 | |||||||
chr1:167680692 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.7-3208C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680692 | |||||||
chr1:167680820 | C | T | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-3080C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680820 | |||||||
chr1:167680969 | A | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(14): Show |
18 | HG01070.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.7-2931A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680969 | |||||||
chr1:167680999 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2901T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167680999 | |||||||
chr1:167681170 | G | T | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.7-2730G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681170 | |||||||
chr1:167681260 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2640T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681260 | |||||||
chr1:167681370 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2530A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681370 | |||||||
chr1:167681414 | G | A | 8 | a0001c0001t0001g0238 a0001c0001t0001g0244 a0001c0001t0008g0219 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2486G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681414 | |||||||
chr1:167681465 | G | A | 5 | a0001c0001t0015g0052 a0001c0001t0015g0239 a0001c0001t0015g0304 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2435G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681465 | |||||||
chr1:167681490 | T | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2410T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681490 | |||||||
chr1:167681666 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7-2234C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681666 | |||||||
chr1:167681668 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-2232C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681668 | |||||||
chr1:167681890 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7-2010G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681890 | |||||||
chr1:167681951 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0013g0198 |
2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.7-1949G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681951 | |||||||
chr1:167681955 | T | C | 4 | a0001c0001t0005g0237 a0001c0001t0023g0227 a0001c0001t0023g0259 others(1): Show |
4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-1945T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167681955 | |||||||
chr1:167682131 | G | A | 5 | a0001c0001t0001g0244 a0001c0001t0008g0219 a0001c0001t0008g0262 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-1769G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682131 | |||||||
chr1:167682172 | C | CT | 23 | a0001c0001t0001g0291 a0001c0001t0001g0328 a0001c0001t0003g0004 others(20): Show |
23 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.7-1713dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682172 | ||||||
chr1:167682172 | C | CTTT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0268 a0001c0001t0001g0279 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1715_7-1713dupTT others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682172 | ||||||
chr1:167682212 | C | G | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-1688C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682212 | |||||||
chr1:167682295 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1605A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682295 | |||||||
chr1:167682378 | A | T | 3 | a0001c0001t0001g0238 a0001c0003t0026g0218 a0001c0003t0026g0303 |
3 | HG01109.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.7-1522A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682378 | |||||||
chr1:167682388 | C | T | 1 | a0001c0001t0039g0337 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7-1512C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682388 | |||||||
chr1:167682406 | T | A | 2 | a0001c0001t0015g0304 a0001c0001t0015g0305 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7-1494T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682406 | |||||||
chr1:167682419 | C | T | 20 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0003g0004 others(17): Show |
20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-1481C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682419 | |||||||
chr1:167682476 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7-1424C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682476 | |||||||
chr1:167682577 | T | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0197 a0001c0001t0004g0124 |
3 | HG00673.hp2 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.7-1323T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682577 | |||||||
chr1:167682668 | A | AGT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(75): Show |
79 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.7-1191_7-1190dupGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | A | AGTGT | 42 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0228 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.7-1193_7-1190dupGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | A | AGTGTGT | 20 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0001c0001t0001g0116 others(17): Show |
20 | HG00423.hp2 HG01109.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.7-1195_7-1190dupGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.7-1199_7-1190dupGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | AGT | A | 51 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(48): Show |
51 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-1191_7-1190delGT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | AGTGT | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0050 others(40): Show |
44 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.7-1193_7-1190delGT others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | AGTGTGT | A | 16 | a0001c0001t0001g0260 a0001c0001t0001g0268 a0001c0001t0001g0270 others(13): Show |
16 | HG02027.hp1 HG02148.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.7-1195_7-1190delGT others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0003g0133 a0001c0001t0011g0100 |
3 | HG00735.hp2 HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.7-1199_7-1190delGT others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682668 | AGTGTGTG others(5): Show |
A | 7 | a0001c0001t0011g0043 a0001c0001t0011g0067 a0001c0001t0011g0274 others(4): Show |
7 | HG01074.hp2 HG01175.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-1201_7-1190delGT others(10): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 167682668 | ||||||
chr1:167682720 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-1180T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682720 | |||||||
chr1:167682727 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0002g0166 a0001c0001t0004g0056 others(1): Show |
4 | HG00438.hp1 HG02027.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-1173G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682727 | |||||||
chr1:167682750 | G | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(98): Show |
101 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.7-1150G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682750 | |||||||
chr1:167682783 | G | GA | 14 | a0001c0001t0001g0003 a0001c0001t0001g0268 a0001c0001t0001g0279 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1117_7-1116insA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682783 | |||||||
chr1:167682885 | C | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0268 a0001c0001t0001g0279 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-1015C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682885 | |||||||
chr1:167682904 | A | C | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-996A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682904 | |||||||
chr1:167682932 | G | A | 20 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0003g0004 others(17): Show |
20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.7-968G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682932 | |||||||
chr1:167682969 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.7-931T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167682969 | |||||||
chr1:167683035 | C | A | 124 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(121): Show |
124 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-865C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683035 | |||||||
chr1:167683103 | G | A | 3 | a0003c0004t0025g0034 a0003c0004t0025g0240 a0006c0007t0017g0242 |
3 | HG02280.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.7-797G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683103 | |||||||
chr1:167683107 | G | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-793G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683107 | |||||||
chr1:167683281 | G | A | 8 | a0001c0001t0005g0111 a0001c0001t0016g0112 a0001c0001t0016g0253 others(5): Show |
8 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-619G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683281 | |||||||
chr1:167683409 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-491T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683409 | |||||||
chr1:167683419 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7-481C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683419 | |||||||
chr1:167683423 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(148): Show |
152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.7-477C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683423 | |||||||
chr1:167683550 | A | C | 2 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.7-350A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683550 | |||||||
chr1:167683575 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7-325G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683575 | |||||||
chr1:167683578 | G | A | 4 | a0001c0001t0005g0237 a0001c0001t0023g0227 a0001c0001t0023g0259 others(1): Show |
4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-322G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683578 | |||||||
chr1:167683703 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.7-197G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683703 | |||||||
chr1:167683758 | C | A | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-142C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683758 | |||||||
chr1:167683765 | G | A | 37 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0003g0004 others(34): Show |
37 | HG01070.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.7-135G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683765 | |||||||
chr1:167683864 | T | C | 1 | a0001c0001t0015g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7-36T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683864 | |||||||
chr1:167683892 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG00140.hp2 | splice_region_variant&intron_variant | LOW | c.7-8T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 1/6 | chr1 | 167683892 | |||||||
chr1:167684039 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.108+38G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684039 | |||||||
chr1:167684404 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.108+403G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684404 | |||||||
chr1:167684422 | G | T | 7 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 others(4): Show |
7 | HG01070.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.108+421G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684422 | |||||||
chr1:167684490 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.108+489G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684490 | |||||||
chr1:167684596 | C | G | 1 | a0001c0001t0013g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.108+595C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684596 | |||||||
chr1:167684612 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+611C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684612 | |||||||
chr1:167684730 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.109-691C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684730 | |||||||
chr1:167684751 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(14): Show |
18 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.109-670G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684751 | |||||||
chr1:167684806 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.109-615G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684806 | |||||||
chr1:167684871 | T | A | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-550T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167684871 | |||||||
chr1:167685000 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.109-421G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685000 | |||||||
chr1:167685102 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.109-319C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685102 | |||||||
chr1:167685120 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-301T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685120 | |||||||
chr1:167685128 | G | A | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-293G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685128 | |||||||
chr1:167685344 | T | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0279 others(14): Show |
18 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.109-77T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685344 | |||||||
chr1:167685361 | C | T | 21 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
21 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.109-60C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685361 | |||||||
chr1:167685407 | C | T | 3 | a0001c0001t0005g0332 a0001c0001t0008g0329 a0001c0001t0008g0331 |
3 | HG01891.hp1 HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.109-14C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 2/6 | chr1 | 167685407 | |||||||
chr1:167685900 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.198+390G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685900 | |||||||
chr1:167685912 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.198+402T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685912 | |||||||
chr1:167685989 | T | C | 1 | a0001c0001t0016g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.198+479T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167685989 | |||||||
chr1:167686005 | C | T | 20 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0003g0004 others(17): Show |
20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.198+495C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686005 | |||||||
chr1:167686020 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0053 |
2 | HG02293.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.198+510G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686020 | |||||||
chr1:167686326 | C | T | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.198+816C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686326 | |||||||
chr1:167686352 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.198+842G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686352 | |||||||
chr1:167686774 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+1264C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686774 | |||||||
chr1:167686864 | G | A | 8 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+1354G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167686864 | |||||||
chr1:167687003 | G | C | 1 | a0001c0001t0004g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198+1493G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687003 | |||||||
chr1:167687120 | G | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0025 others(83): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.198+1610G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687120 | |||||||
chr1:167687139 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.198+1629G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687139 | |||||||
chr1:167687153 | A | G | 15 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(12): Show |
15 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+1643A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687153 | |||||||
chr1:167687221 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.198+1711G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687221 | |||||||
chr1:167687378 | G | GC | 55 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0001g0268 others(52): Show |
55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+1869dupC | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687378 | ||||||
chr1:167687392 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0002g0205 |
3 | HG02074.hp2 NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+1882A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687392 | |||||||
chr1:167687395 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.198+1885C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687395 | |||||||
chr1:167687477 | C | A | 11 | a0001c0001t0005g0111 a0001c0001t0016g0112 a0001c0001t0016g0253 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+1967C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687477 | |||||||
chr1:167687501 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198+1991T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687501 | |||||||
chr1:167687511 | A | G | 1 | a0001c0001t0012g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.198+2001A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687511 | |||||||
chr1:167687522 | C | CA | 33 | a0001c0001t0001g0014 a0001c0001t0001g0131 a0001c0001t0001g0221 others(30): Show |
33 | HG01081.hp2 HG01884.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+2028dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687522 | ||||||
chr1:167687534 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+2024A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687534 | |||||||
chr1:167687539 | G | A | 3 | a0001c0001t0017g0338 a0001c0001t0017g0341 a0001c0001t0021g0005 |
3 | HG03209.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.198+2029G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687539 | |||||||
chr1:167687700 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+2190C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687700 | |||||||
chr1:167687964 | T | C | 3 | a0001c0001t0003g0084 a0001c0001t0003g0130 a0001c0001t0003g0140 |
3 | NA18968.hp1 NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.199-2085T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167687964 | |||||||
chr1:167687995 | C | CTA | 8 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-2045_199-2044d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167687995 | ||||||
chr1:167688126 | C | T | 4 | a0001c0001t0012g0315 a0001c0001t0027g0078 a0001c0001t0027g0089 others(1): Show |
4 | HG00544.hp1 NA18947.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1923C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688126 | |||||||
chr1:167688262 | G | C | 20 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0003g0004 others(17): Show |
20 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.199-1787G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688262 | |||||||
chr1:167688627 | A | T | 1 | a0001c0001t0018g0340 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-1422A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688627 | |||||||
chr1:167688738 | A | C | 19 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0008g0219 others(16): Show |
19 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.199-1311A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688738 | |||||||
chr1:167688969 | A | G | 55 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0001g0268 others(52): Show |
55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-1080A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167688969 | |||||||
chr1:167689002 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199-1047G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689002 | |||||||
chr1:167689078 | A | G | 55 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0001g0268 others(52): Show |
55 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-971A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689078 | |||||||
chr1:167689086 | A | G | 1 | a0001c0001t0007g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.199-963A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689086 | |||||||
chr1:167689095 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-954G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689095 | |||||||
chr1:167689225 | C | T | 2 | a0001c0001t0006g0225 a0001c0001t0006g0226 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.199-824C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689225 | |||||||
chr1:167689226 | G | A | 1 | a0001c0001t0008g0310 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-823G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689226 | |||||||
chr1:167689368 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.199-681G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689368 | |||||||
chr1:167689413 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-636C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689413 | |||||||
chr1:167689475 | T | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-574T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689475 | |||||||
chr1:167689492 | A | AAG | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-556_199-555ins others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 167689492 | ||||||
chr1:167689493 | A | G | 35 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
35 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.199-556A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689493 | |||||||
chr1:167689494 | A | AG | 26 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0005g0111 others(23): Show |
26 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.199-555_199-554ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689494 | |||||||
chr1:167689494 | A | G | 1 | a0001c0001t0021g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-555A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689494 | |||||||
chr1:167689567 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-482C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 3/6 | chr1 | 167689567 | |||||||
chr1:167690227 | A | G | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+107A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690227 | |||||||
chr1:167690466 | G | T | 1 | a0001c0001t0003g0004 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+346G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690466 | |||||||
chr1:167690499 | C | A | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.270+379C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690499 | |||||||
chr1:167690502 | T | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+382T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690502 | |||||||
chr1:167690525 | T | C | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+405T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690525 | |||||||
chr1:167690557 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.270+437C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690557 | |||||||
chr1:167690573 | C | A | 5 | a0001c0001t0001g0244 a0001c0001t0008g0219 a0001c0001t0008g0262 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+453C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690573 | |||||||
chr1:167690626 | G | T | 2 | a0001c0003t0026g0218 a0001c0003t0026g0303 |
2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.270+506G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690626 | |||||||
chr1:167690680 | C | T | 4 | a0001c0001t0005g0237 a0001c0001t0023g0227 a0001c0001t0023g0259 others(1): Show |
4 | HG01070.hp1 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+560C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690680 | |||||||
chr1:167690705 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.270+585G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690705 | |||||||
chr1:167690736 | T | TC | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+616_270+617ins others(1): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690736 | |||||||
chr1:167690749 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+629C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690749 | |||||||
chr1:167690812 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0138 others(5): Show |
9 | HG00741.hp2 HG01123.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+692C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690812 | |||||||
chr1:167690850 | A | G | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+730A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690850 | |||||||
chr1:167690881 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.270+761C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690881 | |||||||
chr1:167690886 | A | G | 2 | a0001c0003t0026g0218 a0001c0003t0026g0303 |
2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.270+766A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690886 | |||||||
chr1:167690915 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+795G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167690915 | |||||||
chr1:167691046 | T | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+926T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691046 | |||||||
chr1:167691262 | T | C | 9 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 others(6): Show |
9 | HG01070.hp1 HG01109.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+1142T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691262 | |||||||
chr1:167691375 | C | T | 1 | a0001c0001t0016g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+1255C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691375 | |||||||
chr1:167691423 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.270+1303G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691423 | |||||||
chr1:167691490 | G | A | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.270+1370G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691490 | |||||||
chr1:167691497 | T | C | 50 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(47): Show |
50 | HG00438.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.270+1377T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691497 | |||||||
chr1:167691533 | G | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0127 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.270+1413G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691533 | |||||||
chr1:167691583 | G | A | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1463G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691583 | |||||||
chr1:167691634 | G | A | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+1514G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691634 | |||||||
chr1:167691654 | C | G | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1534C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691654 | |||||||
chr1:167691698 | C | T | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1578C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691698 | |||||||
chr1:167691884 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0015g0052 a0001c0001t0015g0239 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+1764G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691884 | |||||||
chr1:167691899 | G | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1779G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691899 | |||||||
chr1:167691921 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270+1801T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691921 | |||||||
chr1:167691922 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270+1802C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167691922 | |||||||
chr1:167692085 | CACA | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0004 a0001c0001t0015g0052 others(4): Show |
7 | HG02451.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+1971_270+1973d others(5): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 167692085 | ||||||
chr1:167692223 | C | T | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271-1876C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692223 | |||||||
chr1:167692226 | C | T | 12 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1873C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692226 | |||||||
chr1:167692522 | TA | T | 3 | a0001c0001t0003g0004 a0001c0001t0034g0183 a0001c0001t0047g0065 |
3 | HG00280.hp2 HG01070.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-1576delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692522 | |||||||
chr1:167692523 | A | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1576A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692523 | |||||||
chr1:167692525 | T | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.271-1574T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692525 | |||||||
chr1:167692533 | T | A | 12 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1566T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692533 | |||||||
chr1:167692615 | C | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(3): Show |
6 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-1484C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692615 | |||||||
chr1:167692678 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0016 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.271-1421A>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692678 | |||||||
chr1:167692680 | A | G | 12 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1419A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692680 | |||||||
chr1:167692723 | C | T | 12 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1376C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692723 | |||||||
chr1:167692769 | A | C | 12 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1330A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692769 | |||||||
chr1:167692807 | G | A | 63 | a0001c0001t0001g0260 a0001c0001t0001g0320 a0001c0001t0003g0006 others(60): Show |
63 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.271-1292G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692807 | |||||||
chr1:167692890 | G | A | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1209G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692890 | |||||||
chr1:167692956 | CCAGATA | C | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1142_271-1137d others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167692956 | |||||||
chr1:167693001 | A | G | 11 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-1098A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693001 | |||||||
chr1:167693049 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0244 a0001c0001t0001g0268 others(17): Show |
21 | HG01081.hp2 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-1050A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693049 | |||||||
chr1:167693151 | C | T | 8 | a0001c0001t0003g0004 a0001c0001t0015g0052 a0001c0001t0015g0239 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-948C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693151 | |||||||
chr1:167693203 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.271-896C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693203 | |||||||
chr1:167693288 | G | A | 1 | a0001c0008t0021g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.271-811G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693288 | |||||||
chr1:167693298 | G | A | 5 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0010g0071 others(2): Show |
5 | NA18956.hp1 NA18970.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-801G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693298 | |||||||
chr1:167693394 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.271-705G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693394 | |||||||
chr1:167693426 | C | G | 1 | a0001c0010t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-673C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693426 | |||||||
chr1:167693491 | G | A | 1 | a0001c0001t0005g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-608G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693491 | |||||||
chr1:167693593 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.271-506A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693593 | |||||||
chr1:167693610 | T | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0244 others(69): Show |
73 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.271-489T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693610 | |||||||
chr1:167693657 | C | T | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-442C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693657 | |||||||
chr1:167693814 | A | G | 1 | a0001c0003t0026g0218 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271-285A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693814 | |||||||
chr1:167693872 | TTTTGGAA others(46): Show |
T | 1 | a0005c0012t0011g0234 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.271-225_271-173del others(53): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 167693872 | ||||||
chr1:167693910 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0034g0183 a0001c0001t0047g0065 |
3 | HG00280.hp2 HG01070.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-189A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 4/6 | chr1 | 167693910 | |||||||
chr1:167694355 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.474+53G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694355 | |||||||
chr1:167694392 | A | C | 9 | a0001c0001t0003g0004 a0001c0001t0016g0112 a0001c0001t0016g0253 others(6): Show |
9 | HG00280.hp2 HG01070.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+90A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694392 | |||||||
chr1:167694441 | G | T | 11 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+139G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694441 | |||||||
chr1:167694533 | A | G | 1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.474+231A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694533 | |||||||
chr1:167694579 | T | C | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.474+277T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694579 | |||||||
chr1:167694645 | G | T | 9 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+343G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694645 | |||||||
chr1:167694760 | C | A | 11 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+458C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694760 | |||||||
chr1:167694810 | C | T | 11 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+508C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694810 | |||||||
chr1:167694877 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.474+575T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694877 | |||||||
chr1:167694891 | G | A | 1 | a0001c0001t0005g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474+589G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694891 | |||||||
chr1:167694912 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474+610G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167694912 | |||||||
chr1:167695075 | C | CA | 11 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+783dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695075 | ||||||
chr1:167695271 | A | G | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.474+969A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695271 | |||||||
chr1:167695471 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.474+1169G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695471 | |||||||
chr1:167695538 | A | AT | 11 | a0001c0001t0002g0202 a0001c0001t0005g0020 a0001c0001t0005g0030 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+1254dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | ||||||
chr1:167695538 | A | ATTTTTT | 9 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(6): Show |
9 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+1249_474+1254d others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | ||||||
chr1:167695538 | AT | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.474+1254delT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | ||||||
chr1:167695538 | ATT | A | 9 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0004g0126 others(6): Show |
9 | HG00323.hp2 HG01433.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+1253_474+1254d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167695538 | ||||||
chr1:167695674 | A | G | 43 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0004g0126 others(40): Show |
43 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.474+1372A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695674 | |||||||
chr1:167695827 | T | C | 52 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.475-1272T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167695827 | |||||||
chr1:167696035 | G | A | 10 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-1064G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696035 | |||||||
chr1:167696090 | A | G | 69 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0001g0268 others(66): Show |
69 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.475-1009A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696090 | |||||||
chr1:167696142 | C | T | 10 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-957C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696142 | |||||||
chr1:167696162 | C | T | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.475-937C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696162 | |||||||
chr1:167696169 | G | A | 6 | a0001c0001t0001g0152 a0001c0001t0001g0272 a0001c0001t0002g0163 others(3): Show |
6 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-930G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696169 | |||||||
chr1:167696338 | CTT | C | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.475-760_475-759del others(2): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696338 | |||||||
chr1:167696455 | C | CT | 21 | a0001c0001t0001g0244 a0001c0001t0008g0219 a0001c0001t0008g0262 others(18): Show |
21 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-630dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 167696455 | ||||||
chr1:167696489 | C | T | 21 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(18): Show |
21 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-610C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696489 | |||||||
chr1:167696747 | C | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 |
3 | HG02145.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.475-352C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696747 | |||||||
chr1:167696759 | T | C | 1 | a0001c0009t0005g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.475-340T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696759 | |||||||
chr1:167696797 | C | T | 10 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.475-302C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696797 | |||||||
chr1:167696798 | G | A | 15 | a0001c0001t0001g0221 a0001c0001t0001g0268 a0001c0001t0001g0302 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-301G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696798 | |||||||
chr1:167696935 | T | C | 21 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(18): Show |
21 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.475-164T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696935 | |||||||
chr1:167696981 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0030 a0001c0001t0005g0061 others(17): Show |
20 | HG00438.hp2 HG01074.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.475-118C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167696981 | |||||||
chr1:167697079 | T | C | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.475-20T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 5/6 | chr1 | 167697079 | |||||||
chr1:167697875 | CA | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0059 |
4 | HG03491.hp1 HG03492.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+34delA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697875 | |||||||
chr1:167697917 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0129 others(1): Show |
4 | HG00642.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+75C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697917 | |||||||
chr1:167697925 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1218+83C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697925 | |||||||
chr1:167697954 | A | G | 19 | a0001c0001t0001g0244 a0001c0001t0001g0328 a0001c0001t0008g0219 others(16): Show |
19 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1218+112A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697954 | |||||||
chr1:167697969 | T | C | 4 | a0001c0001t0001g0328 a0001c0001t0022g0241 a0001c0001t0022g0342 others(1): Show |
4 | HG01081.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218+127T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697969 | |||||||
chr1:167697985 | C | G | 1 | a0001c0001t0011g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1218+143C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167697985 | |||||||
chr1:167698113 | C | T | 18 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(15): Show |
18 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1218+271C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698113 | |||||||
chr1:167698121 | G | A | 9 | a0001c0001t0001g0131 a0001c0001t0001g0278 a0001c0001t0001g0298 others(6): Show |
9 | HG00673.hp2 HG02015.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+279G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698121 | |||||||
chr1:167698142 | C | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1218+300C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698142 | |||||||
chr1:167698156 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0281 others(8): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1218+314T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698156 | |||||||
chr1:167698167 | T | G | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+325T>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698167 | |||||||
chr1:167698226 | G | T | 1 | a0001c0008t0021g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1218+384G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698226 | |||||||
chr1:167698271 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(51): Show |
55 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1218+429C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698271 | |||||||
chr1:167698303 | G | A | 13 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0005g0069 others(10): Show |
13 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+461G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698303 | |||||||
chr1:167698383 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0244 others(75): Show |
79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1218+541C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698383 | |||||||
chr1:167698502 | C | T | 12 | a0001c0001t0001g0294 a0001c0001t0004g0095 a0001c0001t0011g0042 others(9): Show |
12 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1218+660C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698502 | |||||||
chr1:167698557 | T | C | 2 | a0001c0001t0042g0215 a0001c0001t0051g0117 |
2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1218+715T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698557 | |||||||
chr1:167698608 | CCTAT | C | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1218+771_1218+774d others(6): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698608 | ||||||
chr1:167698666 | T | C | 2 | a0001c0001t0042g0215 a0001c0001t0051g0117 |
2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1218+824T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698666 | |||||||
chr1:167698690 | C | A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0307 others(8): Show |
11 | HG01496.hp1 HG02083.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1218+848C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698690 | |||||||
chr1:167698772 | G | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0244 others(73): Show |
77 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1218+930G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698772 | |||||||
chr1:167698807 | G | GT | 10 | a0001c0001t0016g0112 a0001c0001t0016g0253 a0001c0001t0016g0327 others(7): Show |
10 | HG00280.hp2 HG01070.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+970dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698807 | ||||||
chr1:167698807 | G | GTT | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+969_1218+970d others(4): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167698807 | ||||||
chr1:167698813 | G | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(290): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1218+971G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698813 | |||||||
chr1:167698853 | G | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(301): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1218+1011G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698853 | |||||||
chr1:167698862 | G | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(301): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1218+1020G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698862 | |||||||
chr1:167698997 | A | C | 2 | a0001c0001t0034g0183 a0001c0001t0047g0065 |
2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1218+1155A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167698997 | |||||||
chr1:167699000 | G | A | 12 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(9): Show |
12 | HG00280.hp2 HG00438.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1218+1158G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699000 | |||||||
chr1:167699094 | G | C | 2 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1218+1252G>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699094 | |||||||
chr1:167699126 | C | CT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0244 a0001c0001t0001g0279 others(22): Show |
26 | HG01081.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1218+1292dupT | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167699126 | ||||||
chr1:167699182 | G | T | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218+1340G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699182 | |||||||
chr1:167699185 | T | C | 1 | a0001c0001t0003g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1218+1343T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699185 | |||||||
chr1:167699517 | C | T | 2 | a0001c0001t0034g0183 a0001c0001t0047g0065 |
2 | HG00280.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1218+1675C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699517 | |||||||
chr1:167699545 | T | C | 1 | a0001c0001t0003g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1218+1703T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699545 | |||||||
chr1:167699639 | T | C | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1218+1797T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699639 | |||||||
chr1:167699711 | C | T | 10 | a0001c0001t0001g0268 a0001c0001t0005g0020 a0001c0001t0005g0030 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+1869C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699711 | |||||||
chr1:167699792 | C | T | 1 | a0001c0001t0046g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1218+1950C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699792 | |||||||
chr1:167699907 | G | A | 1 | a0001c0001t0009g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1218+2065G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167699907 | |||||||
chr1:167700020 | T | A | 16 | a0001c0001t0001g0244 a0001c0001t0008g0219 a0001c0001t0008g0262 others(13): Show |
16 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+2178T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700020 | |||||||
chr1:167700077 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1218+2235T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700077 | |||||||
chr1:167700139 | A | G | 1 | a0001c0001t0047g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1218+2297A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700139 | |||||||
chr1:167700250 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(304): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1218+2408C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700250 | |||||||
chr1:167700419 | C | T | 2 | a0001c0001t0013g0199 a0001c0001t0013g0204 |
2 | NA18983.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1218+2577C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700419 | |||||||
chr1:167700420 | G | T | 2 | a0003c0004t0025g0034 a0003c0004t0025g0240 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1218+2578G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700420 | |||||||
chr1:167700608 | G | A | 2 | a0003c0004t0025g0034 a0003c0004t0025g0240 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1218+2766G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700608 | |||||||
chr1:167700650 | C | CA | 13 | a0001c0001t0001g0023 a0001c0001t0001g0046 a0001c0001t0001g0216 others(10): Show |
13 | HG00741.hp1 HG01884.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1218+2823dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167700650 | ||||||
chr1:167700698 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1218+2856A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700698 | |||||||
chr1:167700859 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1218+3017G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700859 | |||||||
chr1:167700914 | C | A | 3 | a0001c0001t0003g0135 a0001c0001t0007g0142 a0001c0001t0048g0102 |
3 | HG03927.hp1 NA18959.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1218+3072C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167700914 | |||||||
chr1:167701165 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1218+3323C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701165 | |||||||
chr1:167701192 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1218+3350C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701192 | |||||||
chr1:167701202 | C | T | 81 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1218+3360C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701202 | |||||||
chr1:167701230 | C | T | 55 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(52): Show |
55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1218+3388C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701230 | |||||||
chr1:167701252 | G | GTTTC | 47 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0035 others(44): Show |
47 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1219-3348_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(1): Show |
63 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0028 others(60): Show |
64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1219-3352_1219-334 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(5): Show |
24 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(21): Show |
24 | HG00642.hp2 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1219-3356_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(9): Show |
21 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0001g0161 others(18): Show |
21 | HG00639.hp2 HG02083.hp1 HG02148.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219-3360_1219-334 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(13): Show |
16 | a0001c0001t0001g0186 a0001c0001t0001g0254 a0001c0001t0002g0145 others(13): Show |
16 | HG00280.hp2 HG01516.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-3364_1219-334 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(17): Show |
3 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0003g0060 |
3 | HG02004.hp2 HG02698.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1219-3368_1219-334 others(28): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(21): Show |
6 | a0001c0001t0003g0011 a0001c0001t0003g0041 a0001c0001t0003g0214 others(3): Show |
6 | HG00741.hp1 HG01981.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1219-3372_1219-334 others(32): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(25): Show |
1 | a0001c0001t0006g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1219-3376_1219-334 others(36): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(29): Show |
2 | a0001c0001t0019g0099 a0001c0001t0033g0180 |
2 | HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1219-3380_1219-334 others(40): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(41): Show |
1 | a0001c0001t0003g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1219-3392_1219-334 others(52): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTCTTT others(57): Show |
1 | a0001c0001t0003g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1219-3408_1219-334 others(68): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTGTTT others(5): Show |
1 | a0001c0001t0014g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1219-3409_1219-340 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTGTTT others(9): Show |
2 | a0001c0001t0011g0067 a0001c0001t0011g0100 |
2 | HG01243.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1219-3409_1219-340 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTGTTT others(13): Show |
2 | a0001c0001t0014g0177 a0001c0001t0014g0201 |
2 | NA18979.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1219-3409_1219-340 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | G | GTTTGTTT others(21): Show |
1 | a0001c0001t0011g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1219-3409_1219-340 others(32): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTC | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0038 others(23): Show |
26 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1219-3348_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTCTTT others(1): Show |
G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0229 others(12): Show |
16 | HG01109.hp2 HG02109.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-3352_1219-334 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTCTTT others(5): Show |
G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0268 a0001c0001t0005g0237 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-3356_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTCTTT others(9): Show |
G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0261 a0001c0008t0021g0185 |
3 | HG02280.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-3360_1219-334 others(20): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTCTTT others(13): Show |
G | 5 | a0001c0001t0016g0112 a0001c0001t0016g0253 a0001c0001t0016g0327 others(2): Show |
5 | HG02258.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-3364_1219-334 others(24): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701252 | GTTTCTTT others(29): Show |
G | 1 | a0001c0001t0005g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1219-3380_1219-334 others(40): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701252 | ||||||
chr1:167701256 | C | G | 2 | a0001c0001t0011g0042 a0001c0001t0011g0043 |
2 | HG00438.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1219-3408C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701256 | |||||||
chr1:167701277 | T | TTTCTTTC others(60): Show |
1 | a0001c0001t0019g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(71): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701277 | ||||||
chr1:167701312 | C | CTTTCTTT others(5): Show |
1 | a0001c0001t0013g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(16): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701312 | ||||||
chr1:167701316 | CTTTT | C | 4 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0003g0345 others(1): Show |
4 | HG01515.hp1 HG03239.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-3343_1219-334 others(8): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701316 | ||||||
chr1:167701317 | T | TTTCTTTC | 4 | a0001c0001t0001g0216 a0001c0001t0008g0329 a0001c0001t0020g0301 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(11): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | ||||||
chr1:167701317 | T | TTTCTTTC others(4): Show |
4 | a0001c0001t0002g0165 a0001c0001t0002g0168 a0001c0001t0002g0196 others(1): Show |
4 | HG02004.hp1 HG02056.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(15): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | ||||||
chr1:167701317 | T | TTTCTTTC others(8): Show |
2 | a0001c0001t0002g0209 a0001c0001t0049g0211 |
2 | HG00140.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(19): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | ||||||
chr1:167701317 | T | TTTCTTTC others(32): Show |
1 | a0001c0001t0048g0102 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(43): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701317 | ||||||
chr1:167701318 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0055 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1219-3345_1219-334 others(14): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167701318 | ||||||
chr1:167701319 | T | TCTTTC | 3 | a0001c0001t0001g0025 a0001c0001t0005g0020 a0001c0001t0037g0325 |
3 | HG02055.hp1 HG02083.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1219-3345_1219-334 others(9): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701319 | |||||||
chr1:167701320 | T | C | 76 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1219-3344T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701320 | |||||||
chr1:167701321 | T | C | 2 | a0001c0001t0048g0102 a0001c0001t0049g0211 |
2 | NA18961.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1219-3343T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701321 | |||||||
chr1:167701332 | G | A | 5 | a0001c0001t0015g0052 a0001c0001t0015g0239 a0001c0001t0015g0304 others(2): Show |
5 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-3332G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701332 | |||||||
chr1:167701721 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0328 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1219-2943C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701721 | |||||||
chr1:167701808 | G | A | 1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-2856G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701808 | |||||||
chr1:167701921 | C | G | 10 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0067 others(7): Show |
10 | HG00438.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1219-2743C>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167701921 | |||||||
chr1:167702146 | C | T | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2518C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702146 | |||||||
chr1:167702205 | G | A | 95 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(92): Show |
95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1219-2459G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702205 | |||||||
chr1:167702219 | G | A | 55 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(52): Show |
55 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1219-2445G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702219 | |||||||
chr1:167702226 | G | A | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2438G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702226 | |||||||
chr1:167702236 | A | G | 8 | a0001c0001t0016g0112 a0001c0001t0016g0253 a0001c0001t0016g0327 others(5): Show |
8 | HG02258.hp2 HG02922.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219-2428A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702236 | |||||||
chr1:167702272 | C | T | 2 | a0001c0001t0042g0215 a0001c0001t0051g0117 |
2 | HG00408.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1219-2392C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702272 | |||||||
chr1:167702505 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1219-2159G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702505 | |||||||
chr1:167702595 | A | G | 1 | a0001c0001t0041g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219-2069A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702595 | |||||||
chr1:167702632 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1219-2032A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702632 | |||||||
chr1:167702693 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1219-1971C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702693 | |||||||
chr1:167702694 | G | A | 14 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0006g0098 others(11): Show |
14 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1219-1970G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702694 | |||||||
chr1:167702781 | A | C | 14 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0006g0098 others(11): Show |
14 | HG01255.hp2 HG01433.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1219-1883A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702781 | |||||||
chr1:167702786 | AATAAATA others(1): Show |
A | 17 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0006g0098 others(14): Show |
17 | HG01255.hp2 HG01433.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219-1854_1219-184 others(12): Show |
RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167702786 | ||||||
chr1:167702826 | T | C | 2 | a0001c0001t0004g0088 a0001c0001t0004g0120 |
2 | HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1219-1838T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702826 | |||||||
chr1:167702997 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1219-1667C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167702997 | |||||||
chr1:167703013 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-1651G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703013 | |||||||
chr1:167703015 | T | A | 1 | a0001c0001t0001g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1219-1649T>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703015 | |||||||
chr1:167703115 | G | A | 4 | a0001c0001t0021g0005 a0001c0008t0021g0185 a0003c0004t0025g0034 others(1): Show |
4 | HG02280.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-1549G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703115 | |||||||
chr1:167703262 | C | T | 1 | a0001c0001t0007g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1219-1402C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703262 | |||||||
chr1:167703547 | C | T | 2 | a0001c0001t0021g0005 a0001c0008t0021g0185 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1219-1117C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703547 | |||||||
chr1:167703572 | C | T | 81 | a0001c0001t0001g0221 a0001c0001t0001g0302 a0001c0001t0003g0004 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1219-1092C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703572 | |||||||
chr1:167703604 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1219-1060A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703604 | |||||||
chr1:167703615 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0053 |
2 | HG02293.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1219-1049G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703615 | |||||||
chr1:167703650 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1219-1014G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703650 | |||||||
chr1:167703732 | A | G | 57 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1219-932A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703732 | |||||||
chr1:167703956 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1219-708C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167703956 | |||||||
chr1:167704027 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0328 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1219-637A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704027 | |||||||
chr1:167704045 | C | T | 6 | a0001c0001t0021g0005 a0001c0001t0042g0215 a0001c0001t0051g0117 others(3): Show |
6 | HG00408.hp1 HG02280.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1219-619C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704045 | |||||||
chr1:167704046 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0222 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1219-618A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704046 | |||||||
chr1:167704075 | C | A | 3 | a0001c0001t0018g0330 a0001c0001t0018g0339 a0001c0001t0018g0340 |
3 | HG01884.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1219-589C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704075 | |||||||
chr1:167704079 | G | A | 1 | a0001c0001t0051g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1219-585G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704079 | |||||||
chr1:167704205 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1219-459C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704205 | |||||||
chr1:167704232 | G | A | 8 | a0001c0001t0009g0128 a0001c0001t0009g0213 a0001c0001t0009g0290 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-432G>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704232 | |||||||
chr1:167704309 | A | AG | 79 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-352dupG | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167704309 | ||||||
chr1:167704318 | A | G | 79 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-346A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704318 | |||||||
chr1:167704426 | T | C | 8 | a0001c0001t0015g0052 a0001c0001t0015g0239 a0001c0001t0015g0304 others(5): Show |
8 | HG01884.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219-238T>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704426 | |||||||
chr1:167704458 | A | C | 79 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-206A>C | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704458 | |||||||
chr1:167704491 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1219-173A>G | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704491 | |||||||
chr1:167704501 | T | TA | 79 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1219-155dupA | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 167704501 | ||||||
chr1:167704616 | G | T | 11 | a0001c0001t0008g0219 a0001c0001t0008g0262 a0001c0001t0008g0300 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219-48G>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704616 | |||||||
chr1:167704627 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1219-37C>T | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704627 | |||||||
chr1:167704644 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1219-20C>A | RCSD1 | ENSG00000198771.11 | transcript | ENST00000367854.8 | protein_coding | 6/6 | chr1 | 167704644 |