Item | Value |
---|---|
geneid | 22866 |
ensemblid | ENSG00000149970.16 |
hgncid | 19701 |
symbol | CNKSR2 |
name | connector enhancer of kinase suppressor of Ras 2 |
refseq_nuc | NM_014927.5 |
refseq_prot | NP_055742.2 |
ensembl_nuc | ENST00000379510.5 |
ensembl_prot | ENSP00000368824.3 |
mane_status | MANE Select |
chr | chrX |
start | 21374418 |
end | 21654689 |
strand | + |
ver | v1.2 |
region | chrX:21374418-21654689 |
region5000 | chrX:21369418-21659689 |
regionname0 | CNKSR2_chrX_21374418_21654689 |
regionname5000 | CNKSR2_chrX_21369418_21659689 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1034 | 161 | 40 | 29 | 67 | 5 | 18 | 52 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | MALIM others(1029): Show |
chrX | 21369418 | 21659689 |
a0002 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | MALIM others(1029): Show |
chrX | 21369418 | 21659689 |
a0003 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | MALIM others(1029): Show |
chrX | 21369418 | 21659689 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3102 | 148 | 36 | 26 | 61 | 5 | 18 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0001c0002 | 0/0 | 3102 | 8 | 0 | 2 | 6 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0001c0003 | 0/0 | 3102 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0001c0006 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0001c0007 | 0/0 | 3102 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0002c0004 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 | ||
a0003c0005 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | ATGGC others(3097): Show |
chrX | 21369418 | 21659689 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5754 | 44 | 3 | 6 | 23 | 3 | 9 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5749): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0002 | 0/0 | 5751 | 23 | 2 | 5 | 15 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5746): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0003 | 0/0 | 5754 | 12 | 4 | 1 | 5 | 0 | 2 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5749): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0004 | 1/0 | 5753 | 8 | 0 | 1 | 5 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0005 | 0/1 | 5757 | 9 | 0 | 5 | 2 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5752): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0006 | 0/0 | 5756 | 5 | 5 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0007 | 0/0 | 5755 | 4 | 1 | 0 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5750): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0008 | 0/0 | 5752 | 5 | 1 | 1 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5747): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0009 | 0/0 | 5750 | 4 | 4 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5745): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0010 | 0/0 | 5756 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0011 | 0/0 | 5753 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0012 | 0/0 | 5750 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5745): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0013 | 0/0 | 5757 | 2 | 0 | 1 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5752): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0015 | 0/0 | 5758 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5753): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0016 | 0/0 | 5756 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0017 | 0/0 | 5753 | 2 | 0 | 2 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0018 | 0/0 | 5766 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5761): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0019 | 0/0 | 5768 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5763): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0020 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5755): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0021 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5755): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0022 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5754): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0023 | 0/0 | 5766 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5761): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0024 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5754): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0025 | 0/0 | 5756 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0027 | 0/0 | 5756 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0028 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5749): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0029 | 0/0 | 5755 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5750): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0030 | 0/0 | 5755 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5750): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0032 | 0/0 | 5755 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5750): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0033 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5746): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0034 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5745): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0035 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5733): Show |
chrX | 21369418 | 21659689 |
a0001c0001t0036 | 0/0 | 5732 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5727): Show |
chrX | 21369418 | 21659689 |
a0001c0002t0001 | 0/0 | 5754 | 5 | 0 | 2 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5749): Show |
chrX | 21369418 | 21659689 |
a0001c0002t0004 | 0/0 | 5753 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0001c0002t0007 | 0/0 | 5755 | 2 | 0 | 0 | 2 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5750): Show |
chrX | 21369418 | 21659689 |
a0001c0003t0014 | 0/0 | 5777 | 2 | 2 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5772): Show |
chrX | 21369418 | 21659689 |
a0001c0003t0026 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5770): Show |
chrX | 21369418 | 21659689 |
a0001c0006t0004 | 0/0 | 5753 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0001c0007t0031 | 0/0 | 5753 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5748): Show |
chrX | 21369418 | 21659689 |
a0002c0004t0006 | 0/0 | 5756 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5751): Show |
chrX | 21369418 | 21659689 |
a0003c0005t0003 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | GTCAT others(5749): Show |
chrX | 21369418 | 21659689 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0004 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0015g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0016g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0016g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0017g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0017g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0019g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0020g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0023g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0027g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0028g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0029g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0030g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0032g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0034g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0035g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0001t0036g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0002t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0003t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0003t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0003t0026g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0006t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0001c0007t0031g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0002c0004t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
a0003c0005t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | GBR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0087 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0055 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01071 | hp2 | a0001 | c0001 | t0017 | g0017 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01081 | hp1 | a0001 | c0007 | t0031 | g0027 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01109 | hp1 | a0001 | c0001 | t0017 | g0147 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0061 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01243 | hp1 | a0001 | c0001 | t0020 | g0142 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01358 | hp1 | a0001 | c0001 | t0018 | g0123 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01884 | hp1 | a0002 | c0004 | t0006 | g0153 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01884 | hp2 | a0001 | c0001 | t0019 | g0013 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG01952 | hp1 | a0001 | c0001 | t0015 | g0100 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02027 | hp1 | a0001 | c0002 | t0007 | g0040 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0032 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02132 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02300 | hp1 | a0001 | c0001 | t0016 | g0070 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02602 | hp1 | a0001 | c0001 | t0016 | g0031 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02615 | hp1 | a0001 | c0003 | t0014 | g0148 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02647 | hp1 | a0001 | c0001 | t0035 | g0007 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02735 | hp1 | a0001 | c0001 | t0029 | g0079 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02886 | hp2 | a0003 | c0005 | t0003 | g0029 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02965 | hp1 | a0001 | c0003 | t0026 | g0150 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0140 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03098 | hp1 | a0001 | c0001 | t0034 | g0008 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0143 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0160 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0162 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03491 | hp2 | a0001 | c0001 | t0036 | g0136 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03516 | hp2 | a0001 | c0006 | t0004 | g0057 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03654 | hp1 | a0001 | c0001 | t0023 | g0135 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03688 | hp1 | a0001 | c0001 | t0015 | g0038 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | BEB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG04204 | hp1 | a0001 | c0001 | t0032 | g0085 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CHB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18967 | hp1 | a0001 | c0001 | t0030 | g0054 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18977 | hp1 | a0001 | c0002 | t0007 | g0039 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0144 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19000 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19006 | hp1 | a0001 | c0001 | t0028 | g0002 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19012 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19043 | hp1 | a0001 | c0001 | t0033 | g0023 | AFR | LWK | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19060 | hp1 | a0001 | c0001 | t0021 | g0076 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19062 | hp1 | a0001 | c0001 | t0025 | g0130 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19072 | hp1 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19079 | hp1 | a0001 | c0002 | t0004 | g0106 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0163 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0132 | EUR | TSI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG02486 | hp1 | a0001 | c0001 | t0027 | g0033 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
HG03471 | hp1 | a0001 | c0003 | t0014 | g0149 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA18955 | hp1 | a0001 | c0001 | t0013 | g0086 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | USA | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
NA20300 | hp2 | a0001 | c0001 | t0024 | g0155 | AFR | USA | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0004 | REF | REF | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0059 | REF | REF | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:21609542 | C | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2617C>A | p.Pro873Thr | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/22 | 3097/5753 | 2617/3105 | 873/1034 | chrX | 21609542 | |||
chrX:21652399 | G | A | 1 | a0003 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2983G>A | p.Asp995Asn | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3463/5753 | 2983/3105 | 995/1034 | chrX | 21652399 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:21470771 | T | C | 1 | a0001c0003 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.525T>C | p.Cys175Cys | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/22 | 1005/5753 | 525/3105 | 175/1034 | chrX | 21470771 | |||
chrX:21490548 | A | G | 1 | a0001c0002 | 8 | HG01934.hp1 HG01943.hp1 HG02027.hp1 others(5): Show |
synonymous_variant | LOW | c.651A>G | p.Gln217Gln | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/22 | 1131/5753 | 651/3105 | 217/1034 | chrX | 21490548 | |||
chrX:21652342 | C | T | 1 | a0001c0007 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.2926C>T | p.Leu976Leu | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3406/5753 | 2926/3105 | 976/1034 | chrX | 21652342 | |||
chrX:21652512 | G | A | 1 | a0001c0006 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.3096G>A | p.Thr1032Thr | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3576/5753 | 3096/3105 | 1032/1034 | chrX | 21652512 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:21374594 | G | GGCA | 3 | a0001c0001t0013 a0001c0001t0024 a0001c0001t0025 |
4 | HG01167.hp1 NA18955.hp1 NA19062.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-266dupAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374594 | G | GGCAGCA | 3 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0022 |
3 | HG01243.hp1 HG02055.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-271_-266dupAGCAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374594 | G | GGCAGCAG others(5): Show |
1 | a0001c0001t0018 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-277_-266dupAGCAGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374594 | GGCA | G | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(4): Show |
39 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-266delAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374594 | GGCAGCAG others(8): Show |
G | 1 | a0001c0001t0035 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-280_-266delAGCAGC others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374594 | GGCAGCAG others(14): Show |
G | 1 | a0001c0001t0036 | 1 | HG03491.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286_-266delAGCAGC others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | |||||
chrX:21374630 | A | AGCAGCAG others(5): Show |
1 | a0001c0001t0019 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-266_-265insAGCAGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374630 | |||||
chrX:21374630 | A | AGCAGCCG others(5): Show |
1 | a0001c0001t0023 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266_-265insAGCCGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374630 | |||||
chrX:21374630 | A | AGCC | 3 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0016 |
12 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-252_-250dupGCC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 249 | INFO_REALIGN_3_PRIME | chrX | 21374630 | |||||
chrX:21374630 | A | AGCCGCAG others(14): Show |
2 | a0001c0003t0014 a0001c0003t0026 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-263_-262insAGCAGC others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 262 | INFO_REALIGN_3_PRIME | chrX | 21374630 | |||||
chrX:21374630 | A | C | 10 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(7): Show |
25 | HG01081.hp1 HG01081.hp2 HG02280.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-268A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 268 | chrX | 21374630 | ||||||
chrX:21374633 | C | A | 1 | a0001c0001t0020 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-265C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | chrX | 21374633 | ||||||
chrX:21374772 | G | A | 2 | a0001c0003t0014 a0001c0003t0026 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-126G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 126 | chrX | 21374772 | ||||||
chrX:21652832 | T | G | 1 | a0001c0001t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 311 | chrX | 21652832 | ||||||
chrX:21652977 | C | A | 1 | a0001c0001t0029 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 456 | chrX | 21652977 | ||||||
chrX:21653480 | A | T | 1 | a0001c0001t0028 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 959 | chrX | 21653480 | ||||||
chrX:21653606 | T | A | 1 | a0001c0001t0028 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1085 | chrX | 21653606 | ||||||
chrX:21653808 | G | A | 1 | a0001c0001t0035 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1287G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1287 | chrX | 21653808 | ||||||
chrX:21654098 | A | T | 1 | a0001c0001t0028 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1577 | chrX | 21654098 | ||||||
chrX:21654113 | A | C | 1 | a0001c0001t0028 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1592 | chrX | 21654113 | ||||||
chrX:21654269 | A | ATG | 2 | a0001c0001t0029 a0001c0001t0032 |
2 | HG02735.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1750_*1751dupGT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1752 | INFO_REALIGN_3_PRIME | chrX | 21654269 | |||||
chrX:21654272 | T | TA | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(11): Show |
102 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1773dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | |||||
chrX:21654272 | T | TAA | 5 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 others(2): Show |
14 | HG01069.hp1 HG01952.hp1 HG02027.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1772_*1773dupAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | |||||
chrX:21654272 | T | TAAA | 8 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0017 others(5): Show |
16 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1771_*1773dupAAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | |||||
chrX:21654287 | A | C | 3 | a0001c0001t0009 a0001c0001t0034 a0001c0001t0035 |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1766A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1766 | chrX | 21654287 | ||||||
chrX:21654288 | A | C | 1 | a0001c0007t0031 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1767 | chrX | 21654288 | ||||||
chrX:21654295 | C | A | 1 | a0001c0001t0025 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | chrX | 21654295 | ||||||
chrX:21654296 | A | C | 1 | a0001c0001t0025 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1775 | chrX | 21654296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:21375244 | C | G | 12 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+283C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375244 | |||||||
chrX:21375625 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64+664G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375625 | |||||||
chrX:21375918 | C | T | 1 | a0001c0001t0008g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64+957C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375918 | |||||||
chrX:21376153 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1192A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376153 | |||||||
chrX:21376601 | C | T | 1 | a0001c0001t0017g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+1640C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376601 | |||||||
chrX:21376778 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.64+1817A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376778 | |||||||
chrX:21377049 | G | A | 1 | a0001c0001t0028g0002 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.64+2088G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377049 | |||||||
chrX:21377618 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0008g0144 |
2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.64+2657G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377618 | |||||||
chrX:21377901 | A | T | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+2940A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377901 | |||||||
chrX:21377911 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.64+2950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377911 | |||||||
chrX:21378232 | A | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+3271A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21378232 | |||||||
chrX:21378261 | C | A | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+3300C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21378261 | |||||||
chrX:21379575 | T | G | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.64+4614T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21379575 | |||||||
chrX:21380310 | C | T | 1 | a0001c0001t0011g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+5349C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380310 | |||||||
chrX:21380443 | C | CT | 5 | a0001c0001t0001g0139 a0001c0001t0002g0145 a0001c0001t0003g0138 others(2): Show |
5 | HG03490.hp1 NA18965.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+5503dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | ||||||
chrX:21380443 | CT | C | 31 | a0001c0001t0001g0157 a0001c0001t0002g0006 a0001c0001t0002g0018 others(28): Show |
31 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.64+5503delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | ||||||
chrX:21380443 | CTT | C | 15 | a0001c0001t0003g0014 a0001c0001t0003g0152 a0001c0001t0007g0141 others(12): Show |
15 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+5502_64+5503del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | ||||||
chrX:21380634 | C | G | 33 | a0001c0001t0001g0157 a0001c0001t0003g0014 a0001c0001t0003g0152 others(30): Show |
33 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.64+5673C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380634 | |||||||
chrX:21380722 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0003g0134 |
2 | HG02071.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.64+5761A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380722 | |||||||
chrX:21380739 | C | T | 2 | a0001c0001t0005g0132 a0001c0001t0016g0031 |
2 | HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.64+5778C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380739 | |||||||
chrX:21381138 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+6177G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381138 | |||||||
chrX:21381225 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+6264C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381225 | |||||||
chrX:21381649 | A | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+6688A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381649 | |||||||
chrX:21381690 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+6729G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381690 | |||||||
chrX:21381910 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.64+6949C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381910 | |||||||
chrX:21382102 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64+7141C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21382102 | |||||||
chrX:21382859 | C | G | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.64+7898C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21382859 | |||||||
chrX:21383652 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.64+8691C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21383652 | |||||||
chrX:21384319 | A | T | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+9358A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21384319 | |||||||
chrX:21384626 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.64+9665A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21384626 | |||||||
chrX:21385318 | A | G | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.64+10357A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21385318 | |||||||
chrX:21386018 | C | CA | 32 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(29): Show |
32 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+11081dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21386018 | ||||||
chrX:21386018 | CA | C | 9 | a0001c0001t0003g0014 a0001c0001t0007g0127 a0001c0001t0011g0015 others(6): Show |
9 | HG02615.hp1 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+11081delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21386018 | ||||||
chrX:21386428 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+11467T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386428 | |||||||
chrX:21386611 | A | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.64+11650A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386611 | |||||||
chrX:21386713 | A | G | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.64+11752A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386713 | |||||||
chrX:21386845 | A | G | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.64+11884A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386845 | |||||||
chrX:21387080 | T | C | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+12119T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387080 | |||||||
chrX:21387855 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.64+12894C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387855 | |||||||
chrX:21387990 | C | A | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.64+13029C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387990 | |||||||
chrX:21388086 | A | G | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64+13125A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388086 | |||||||
chrX:21388338 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+13377A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388338 | |||||||
chrX:21388979 | T | C | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64+14018T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388979 | |||||||
chrX:21389119 | C | T | 13 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(10): Show |
13 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+14158C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389119 | |||||||
chrX:21389120 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+14159G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389120 | |||||||
chrX:21389258 | C | T | 8 | a0001c0001t0002g0045 a0001c0001t0002g0118 a0001c0001t0002g0119 others(5): Show |
8 | HG02083.hp1 NA18612.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+14297C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389258 | |||||||
chrX:21389721 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.64+14760A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389721 | |||||||
chrX:21390356 | A | G | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64+15395A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390356 | |||||||
chrX:21390535 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+15574A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390535 | |||||||
chrX:21390688 | C | T | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64+15727C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390688 | |||||||
chrX:21391166 | A | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+16205A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391166 | |||||||
chrX:21391470 | C | G | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+16509C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391470 | |||||||
chrX:21391479 | T | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+16518T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391479 | |||||||
chrX:21391533 | G | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+16572G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391533 | |||||||
chrX:21391632 | C | G | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.64+16671C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391632 | |||||||
chrX:21391713 | C | T | 1 | a0001c0001t0034g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64+16752C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391713 | |||||||
chrX:21391884 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.64+16923C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391884 | |||||||
chrX:21392162 | G | GT | 15 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(12): Show |
15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+17202dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21392162 | ||||||
chrX:21392426 | G | A | 3 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0140 |
3 | HG02717.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64+17465G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392426 | |||||||
chrX:21392481 | T | A | 15 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(12): Show |
15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+17520T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392481 | |||||||
chrX:21392949 | TC | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+17990delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21392949 | ||||||
chrX:21392968 | T | C | 12 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(9): Show |
12 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+18007T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392968 | |||||||
chrX:21393074 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.64+18113T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393074 | |||||||
chrX:21393293 | C | T | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64+18332C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393293 | |||||||
chrX:21393507 | C | A | 1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64+18546C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393507 | |||||||
chrX:21393876 | T | C | 5 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+18915T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393876 | |||||||
chrX:21394370 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | NA18944.hp1 NA19000.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+19409G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394370 | |||||||
chrX:21394427 | C | G | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+19466C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394427 | |||||||
chrX:21394594 | G | C | 15 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(12): Show |
15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+19633G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394594 | |||||||
chrX:21394900 | G | T | 69 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(66): Show |
69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.64+19939G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394900 | |||||||
chrX:21395319 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64+20358A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21395319 | |||||||
chrX:21395413 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.64+20452G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21395413 | |||||||
chrX:21396442 | A | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+21481A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396442 | |||||||
chrX:21396457 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+21496A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396457 | |||||||
chrX:21396577 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.64+21616C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396577 | |||||||
chrX:21398302 | C | T | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64+23341C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398302 | |||||||
chrX:21398340 | A | G | 8 | a0001c0002t0001g0041 a0001c0002t0001g0104 a0001c0002t0001g0105 others(5): Show |
8 | HG01934.hp1 HG01943.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+23379A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398340 | |||||||
chrX:21398390 | T | C | 2 | a0001c0001t0006g0154 a0002c0004t0006g0153 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.64+23429T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398390 | |||||||
chrX:21398498 | T | C | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+23537T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398498 | |||||||
chrX:21399197 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24236A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399197 | |||||||
chrX:21399551 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24590G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399551 | |||||||
chrX:21399632 | T | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24671T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399632 | |||||||
chrX:21399648 | A | G | 15 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(12): Show |
15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+24687A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399648 | |||||||
chrX:21399685 | T | C | 12 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(9): Show |
12 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+24724T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399685 | |||||||
chrX:21399752 | C | T | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.64+24791C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399752 | |||||||
chrX:21399983 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64+25022T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399983 | |||||||
chrX:21400142 | A | G | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64+25181A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400142 | |||||||
chrX:21400469 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.64+25508A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400469 | |||||||
chrX:21400553 | T | C | 41 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(38): Show |
41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+25592T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400553 | |||||||
chrX:21400631 | G | A | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64+25670G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400631 | |||||||
chrX:21401316 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.65-25181C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401316 | |||||||
chrX:21401536 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-24961C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401536 | |||||||
chrX:21401675 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.65-24822G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401675 | |||||||
chrX:21401840 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0051 |
2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.65-24657G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401840 | |||||||
chrX:21402190 | A | C | 1 | a0001c0001t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-24307A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402190 | |||||||
chrX:21402614 | A | G | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-23883A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402614 | |||||||
chrX:21402626 | T | G | 39 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(36): Show |
39 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.65-23871T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402626 | |||||||
chrX:21402693 | A | G | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-23804A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402693 | |||||||
chrX:21403015 | G | T | 47 | a0001c0001t0001g0157 a0001c0001t0002g0006 a0001c0001t0002g0018 others(44): Show |
47 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.65-23482G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403015 | |||||||
chrX:21403057 | G | A | 12 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-23440G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403057 | |||||||
chrX:21403128 | A | G | 70 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(67): Show |
70 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.65-23369A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403128 | |||||||
chrX:21403543 | T | C | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-22954T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403543 | |||||||
chrX:21403580 | A | G | 19 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0024 others(16): Show |
19 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-22917A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403580 | |||||||
chrX:21403850 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-22647T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403850 | |||||||
chrX:21403927 | C | T | 1 | a0001c0001t0027g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-22570C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403927 | |||||||
chrX:21404789 | C | CA | 22 | a0001c0001t0001g0035 a0001c0001t0002g0026 a0001c0001t0002g0110 others(19): Show |
22 | HG00609.hp1 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-21685dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21404789 | ||||||
chrX:21404789 | CA | C | 5 | a0001c0001t0001g0139 a0001c0001t0002g0018 a0001c0001t0002g0046 others(2): Show |
5 | HG01106.hp1 HG03490.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-21685delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21404789 | ||||||
chrX:21406148 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.65-20349G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406148 | |||||||
chrX:21406420 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-20077T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406420 | |||||||
chrX:21406815 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.65-19682G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406815 | |||||||
chrX:21407002 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-19495T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407002 | |||||||
chrX:21407528 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.65-18969C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407528 | |||||||
chrX:21407555 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18942G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407555 | |||||||
chrX:21407557 | T | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18940T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407557 | |||||||
chrX:21407558 | GT | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18934delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21407558 | ||||||
chrX:21407734 | G | A | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-18763G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407734 | |||||||
chrX:21408471 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(155): Show |
158 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.65-18026A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21408471 | |||||||
chrX:21408965 | A | T | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.65-17532A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21408965 | |||||||
chrX:21409107 | T | C | 1 | a0001c0001t0003g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-17390T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409107 | |||||||
chrX:21409226 | AATTATAT others(4): Show |
A | 1 | a0001c0001t0008g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65-17268_65-17258d others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409226 | ||||||
chrX:21409228 | T | TTATATA | 3 | a0001c0001t0002g0003 a0001c0001t0022g0032 a0001c0001t0036g0136 |
3 | HG00621.hp1 HG02055.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.65-17223_65-17218d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | T | TTATATAT others(3): Show |
1 | a0001c0003t0014g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.65-17227_65-17218d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTA | T | 7 | a0001c0001t0002g0125 a0001c0001t0004g0088 a0001c0001t0005g0087 others(4): Show |
7 | HG00738.hp1 HG01071.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-17219_65-17218d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATA | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0093 others(5): Show |
8 | HG00673.hp1 HG01192.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-17221_65-17218d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATA | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0099 others(6): Show |
9 | HG01167.hp1 HG02027.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-17223_65-17218d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(1): Show |
T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0089 a0001c0001t0002g0114 others(10): Show |
13 | HG00140.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-17225_65-17218d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(3): Show |
T | 22 | a0001c0001t0001g0050 a0001c0001t0001g0075 a0001c0001t0001g0081 others(19): Show |
22 | HG00609.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-17227_65-17218d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(5): Show |
T | 24 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0062 others(21): Show |
24 | HG00280.hp1 HG00735.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-17229_65-17218d others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(7): Show |
T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0051 others(45): Show |
48 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.65-17231_65-17218d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(9): Show |
T | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0003g0014 others(9): Show |
12 | HG01243.hp1 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-17233_65-17218d others(18): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(11): Show |
T | 4 | a0001c0001t0002g0126 a0001c0001t0003g0030 a0001c0001t0009g0010 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-17235_65-17218d others(20): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(13): Show |
T | 4 | a0001c0001t0002g0006 a0001c0001t0004g0068 a0001c0001t0008g0005 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-17237_65-17218d others(22): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409228 | TTATATAT others(19): Show |
T | 2 | a0001c0001t0009g0009 a0001c0001t0034g0008 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-17243_65-17218d others(28): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | ||||||
chrX:21409272 | A | T | 1 | a0001c0001t0015g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-17225A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409272 | |||||||
chrX:21409389 | G | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-17108G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409389 | |||||||
chrX:21409555 | G | C | 2 | a0001c0001t0002g0145 a0001c0001t0008g0144 |
2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.65-16942G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409555 | |||||||
chrX:21410032 | C | CTG | 34 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0045 others(31): Show |
34 | HG00621.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-16433_65-16432d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | ||||||
chrX:21410032 | C | CTGTG | 2 | a0001c0001t0011g0016 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.65-16435_65-16432d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | ||||||
chrX:21410032 | CTG | C | 10 | a0001c0001t0002g0018 a0001c0001t0002g0026 a0001c0001t0003g0024 others(7): Show |
10 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-16433_65-16432d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | ||||||
chrX:21410032 | CTGTG | C | 13 | a0001c0001t0001g0157 a0001c0001t0006g0156 a0001c0001t0006g0158 others(10): Show |
13 | HG01109.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-16435_65-16432d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | ||||||
chrX:21410046 | G | GTGTT | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-16448_65-16447i others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410046 | ||||||
chrX:21410645 | C | A | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.65-15852C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410645 | |||||||
chrX:21410790 | T | TTG | 7 | a0001c0001t0007g0141 a0001c0001t0009g0009 a0001c0001t0009g0010 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-15681_65-15680d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410790 | ||||||
chrX:21410790 | TTG | T | 4 | a0001c0001t0001g0099 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-15681_65-15680d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410790 | ||||||
chrX:21410906 | G | A | 1 | a0001c0001t0027g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-15591G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410906 | |||||||
chrX:21410964 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-15533A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410964 | |||||||
chrX:21411032 | ACTTTT | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15459_65-15455d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21411032 | ||||||
chrX:21411253 | A | G | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-15244A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411253 | |||||||
chrX:21411297 | C | T | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-15200C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411297 | |||||||
chrX:21411330 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15167G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411330 | |||||||
chrX:21411454 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15043G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411454 | |||||||
chrX:21412034 | C | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-14463C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412034 | |||||||
chrX:21412567 | T | G | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-13930T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412567 | |||||||
chrX:21412657 | A | G | 1 | a0001c0001t0009g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-13840A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412657 | |||||||
chrX:21414305 | A | C | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-12192A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414305 | |||||||
chrX:21414419 | AT | A | 7 | a0001c0001t0013g0061 a0001c0002t0001g0041 a0001c0002t0001g0104 others(4): Show |
7 | HG01167.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-12067delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21414419 | ||||||
chrX:21414487 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.65-12010G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414487 | |||||||
chrX:21414548 | C | G | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.65-11949C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414548 | |||||||
chrX:21414603 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-11894T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414603 | |||||||
chrX:21414975 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0004g0022 |
2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.65-11522C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414975 | |||||||
chrX:21415235 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-11262G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415235 | |||||||
chrX:21415547 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.65-10950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415547 | |||||||
chrX:21415596 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | NA18948.hp1 NA18959.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-10901C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415596 | |||||||
chrX:21415756 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.65-10741G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415756 | |||||||
chrX:21415827 | CAT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
10 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-10664_65-10663d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415827 | ||||||
chrX:21415833 | TAC | T | 75 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0047 others(72): Show |
75 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.65-10626_65-10625d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415833 | TACAC | T | 27 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0001g0157 others(24): Show |
27 | HG01081.hp1 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.65-10628_65-10625d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415833 | TACACAC | T | 8 | a0001c0001t0001g0096 a0001c0001t0002g0111 a0001c0001t0002g0112 others(5): Show |
8 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-10630_65-10625d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415833 | TACACACA others(1): Show |
T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0045 others(13): Show |
16 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-10632_65-10625d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415833 | TACACACA others(3): Show |
T | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-10634_65-10625d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415833 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.65-10638_65-10625d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | ||||||
chrX:21415865 | CACACACA others(1): Show |
C | 2 | a0001c0001t0002g0145 a0001c0001t0008g0144 |
2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.65-10630_65-10623d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415865 | ||||||
chrX:21415867 | C | T | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-10630C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415867 | |||||||
chrX:21415869 | C | T | 14 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(11): Show |
14 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-10628C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415869 | |||||||
chrX:21415869 | CACAT | C | 3 | a0001c0001t0005g0087 a0001c0001t0022g0032 a0001c0001t0027g0033 |
3 | HG00738.hp1 HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-10626_65-10623d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415869 | ||||||
chrX:21415871 | C | T | 20 | a0001c0001t0003g0014 a0001c0001t0003g0024 a0001c0001t0003g0082 others(17): Show |
20 | HG01071.hp2 HG01884.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-10626C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415871 | |||||||
chrX:21416854 | C | CTTTG | 42 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(39): Show |
42 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.65-9640_65-9639ins others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21416854 | ||||||
chrX:21416932 | CTTATCTT others(2): Show |
C | 2 | a0001c0001t0001g0058 a0001c0006t0004g0057 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-9558_65-9550del others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21416932 | ||||||
chrX:21417056 | A | G | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-9441A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417056 | |||||||
chrX:21417172 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.65-9325C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417172 | |||||||
chrX:21417706 | T | C | 1 | a0001c0001t0004g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.65-8791T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417706 | |||||||
chrX:21418276 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-8221G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418276 | |||||||
chrX:21418562 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.65-7935A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418562 | |||||||
chrX:21418831 | T | G | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-7666T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418831 | |||||||
chrX:21418938 | A | G | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.65-7559A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418938 | |||||||
chrX:21419623 | G | A | 1 | a0001c0001t0005g0053 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.65-6874G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21419623 | |||||||
chrX:21419757 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.65-6740A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21419757 | |||||||
chrX:21420245 | A | G | 1 | a0001c0001t0022g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-6252A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21420245 | |||||||
chrX:21420982 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-5515T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21420982 | |||||||
chrX:21421287 | GT | G | 10 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0071 others(7): Show |
10 | HG01167.hp1 HG02300.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5191delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21421287 | ||||||
chrX:21421431 | G | T | 4 | a0001c0001t0022g0032 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-5066G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21421431 | |||||||
chrX:21421812 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4685G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21421812 | |||||||
chrX:21422091 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-4406C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21422091 | |||||||
chrX:21422504 | A | G | 1 | a0001c0001t0022g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-3993A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21422504 | |||||||
chrX:21423189 | A | C | 1 | a0001c0002t0004g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.65-3308A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423189 | |||||||
chrX:21423229 | A | G | 1 | a0001c0001t0016g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-3268A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423229 | |||||||
chrX:21423368 | A | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-3129A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423368 | |||||||
chrX:21423723 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0004g0072 |
3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.65-2774T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423723 | |||||||
chrX:21423897 | T | G | 4 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2600T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423897 | |||||||
chrX:21424152 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | NA18984.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.65-2345A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424152 | |||||||
chrX:21424168 | T | C | 7 | a0001c0001t0007g0141 a0001c0001t0020g0142 a0001c0001t0035g0007 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2329T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424168 | |||||||
chrX:21424401 | C | T | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-2096C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424401 | |||||||
chrX:21424482 | C | G | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-2015C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424482 | |||||||
chrX:21424805 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.65-1692T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424805 | |||||||
chrX:21424877 | A | G | 1 | a0001c0001t0015g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-1620A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424877 | |||||||
chrX:21425121 | C | G | 5 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-1376C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425121 | |||||||
chrX:21425747 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.65-750A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425747 | |||||||
chrX:21425934 | A | G | 5 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 others(2): Show |
5 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-563A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425934 | |||||||
chrX:21426336 | C | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-161C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21426336 | |||||||
chrX:21426358 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-139C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21426358 | |||||||
chrX:21426730 | TCTC | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18948.hp1 NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.228+74_228+76delCT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 21426730 | ||||||
chrX:21426734 | C | T | 69 | a0001c0001t0001g0157 a0001c0001t0002g0006 a0001c0001t0002g0018 others(66): Show |
69 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.228+74C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426734 | |||||||
chrX:21426747 | C | T | 36 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(33): Show |
36 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.228+87C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426747 | |||||||
chrX:21426772 | T | C | 37 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(34): Show |
37 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.228+112T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426772 | |||||||
chrX:21427080 | A | T | 1 | a0001c0001t0002g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.228+420A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427080 | |||||||
chrX:21427195 | T | G | 2 | a0001c0001t0003g0060 a0001c0001t0025g0130 |
2 | NA18970.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.228+535T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427195 | |||||||
chrX:21427273 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.228+613A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427273 | |||||||
chrX:21427297 | A | G | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.228+637A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427297 | |||||||
chrX:21427601 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.228+941C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427601 | |||||||
chrX:21427881 | A | G | 9 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+1221A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427881 | |||||||
chrX:21428532 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.228+1872A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428532 | |||||||
chrX:21428578 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.228+1918A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428578 | |||||||
chrX:21428926 | T | C | 1 | a0001c0001t0023g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.228+2266T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428926 | |||||||
chrX:21429349 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0003g0134 |
2 | HG02071.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.228+2689A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429349 | |||||||
chrX:21429813 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.229-2799G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429813 | |||||||
chrX:21429990 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.229-2622G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429990 | |||||||
chrX:21430030 | A | T | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.229-2582A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430030 | |||||||
chrX:21430426 | T | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.229-2186T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430426 | |||||||
chrX:21430639 | A | G | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.229-1973A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430639 | |||||||
chrX:21431172 | T | C | 4 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-1440T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431172 | |||||||
chrX:21431687 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.229-925C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431687 | |||||||
chrX:21431696 | A | T | 1 | a0001c0001t0013g0061 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.229-916A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431696 | |||||||
chrX:21432337 | A | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.229-275A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21432337 | |||||||
chrX:21432472 | G | A | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.229-140G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21432472 | |||||||
chrX:21432909 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+95G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21432909 | |||||||
chrX:21433077 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.431+263G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21433077 | |||||||
chrX:21433550 | C | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+736C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21433550 | |||||||
chrX:21433653 | T | TAC | 13 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0065 others(10): Show |
13 | HG01071.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+880_431+881dup others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21433653 | T | TACAC | 3 | a0001c0001t0001g0097 a0001c0001t0019g0013 a0001c0001t0034g0008 |
3 | HG01884.hp2 HG03098.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.431+878_431+881dup others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21433653 | T | TACACAC | 2 | a0001c0001t0001g0096 a0001c0001t0009g0009 |
2 | HG03486.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.431+876_431+881dup others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21433653 | T | TACACACA others(3): Show |
2 | a0001c0001t0009g0010 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.431+872_431+881dup others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21433653 | TAC | T | 16 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0092 others(13): Show |
16 | HG00735.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+880_431+881del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21433653 | TACAC | T | 6 | a0001c0001t0001g0052 a0001c0001t0002g0118 a0001c0001t0002g0121 others(3): Show |
6 | HG00280.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+878_431+881del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | ||||||
chrX:21434139 | G | A | 69 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(66): Show |
69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.431+1325G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434139 | |||||||
chrX:21434183 | C | T | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431+1369C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434183 | |||||||
chrX:21434634 | T | G | 9 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+1820T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434634 | |||||||
chrX:21435382 | T | A | 5 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+2568T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21435382 | |||||||
chrX:21435743 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.431+2929T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21435743 | |||||||
chrX:21436044 | C | A | 4 | a0001c0001t0035g0007 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3230C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436044 | |||||||
chrX:21436171 | C | T | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431+3357C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436171 | |||||||
chrX:21436358 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.431+3544A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436358 | |||||||
chrX:21436558 | T | C | 1 | a0001c0001t0023g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.431+3744T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436558 | |||||||
chrX:21437392 | C | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432-3302C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437392 | |||||||
chrX:21437419 | G | GT | 17 | a0001c0001t0001g0064 a0001c0001t0001g0109 a0001c0001t0001g0157 others(14): Show |
17 | HG00621.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-3255dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21437419 | ||||||
chrX:21437419 | GT | G | 8 | a0001c0001t0001g0089 a0001c0001t0003g0116 a0001c0001t0004g0088 others(5): Show |
8 | HG02015.hp1 HG02886.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.432-3255delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21437419 | ||||||
chrX:21437551 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-3143C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437551 | |||||||
chrX:21437609 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432-3085G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437609 | |||||||
chrX:21437715 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.432-2979G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437715 | |||||||
chrX:21437751 | G | T | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432-2943G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437751 | |||||||
chrX:21438097 | T | A | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2597T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438097 | |||||||
chrX:21438098 | G | C | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2596G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438098 | |||||||
chrX:21438100 | T | C | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2594T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438100 | |||||||
chrX:21438101 | A | T | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2593A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438101 | |||||||
chrX:21438107 | T | C | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2587T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438107 | |||||||
chrX:21438110 | C | T | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2584C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438110 | |||||||
chrX:21438111 | A | G | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2583A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438111 | |||||||
chrX:21438112 | A | T | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2582A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438112 | |||||||
chrX:21438338 | A | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.432-2356A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438338 | |||||||
chrX:21438426 | G | C | 1 | a0001c0001t0007g0020 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.432-2268G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438426 | |||||||
chrX:21438580 | T | G | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.432-2114T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438580 | |||||||
chrX:21438860 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1834G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438860 | |||||||
chrX:21438862 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1832G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438862 | |||||||
chrX:21438919 | A | G | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.432-1775A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438919 | |||||||
chrX:21439416 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1278C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439416 | |||||||
chrX:21439544 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.432-1150C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439544 | |||||||
chrX:21439554 | A | C | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.432-1140A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439554 | |||||||
chrX:21439616 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.432-1078A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439616 | |||||||
chrX:21439633 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1061A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439633 | |||||||
chrX:21439702 | C | T | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.432-992C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439702 | |||||||
chrX:21439748 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.432-946A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439748 | |||||||
chrX:21439952 | A | C | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.432-742A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439952 | |||||||
chrX:21440277 | A | G | 17 | a0001c0001t0003g0014 a0001c0001t0003g0024 a0001c0001t0009g0009 others(14): Show |
17 | HG01071.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.432-417A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440277 | |||||||
chrX:21440371 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-323G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440371 | |||||||
chrX:21440575 | G | C | 1 | a0001c0001t0016g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.432-119G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440575 | |||||||
chrX:21440846 | T | A | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.519+65T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21440846 | |||||||
chrX:21441035 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.519+254G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441035 | |||||||
chrX:21441037 | T | G | 1 | a0001c0001t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.519+256T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441037 | |||||||
chrX:21441172 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.519+391A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441172 | |||||||
chrX:21441568 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0002g0003 a0001c0001t0002g0045 others(19): Show |
22 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+787C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441568 | |||||||
chrX:21441765 | A | G | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.519+984A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441765 | |||||||
chrX:21441928 | A | T | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.519+1147A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441928 | |||||||
chrX:21442223 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1442C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442223 | |||||||
chrX:21442425 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18948.hp1 NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.519+1644C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442425 | |||||||
chrX:21442501 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+1720C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442501 | |||||||
chrX:21442643 | G | T | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+1862G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442643 | |||||||
chrX:21442684 | T | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+1903T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442684 | |||||||
chrX:21442895 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+2114A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442895 | |||||||
chrX:21443583 | C | T | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.519+2802C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21443583 | |||||||
chrX:21443765 | C | A | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+2984C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21443765 | |||||||
chrX:21444301 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+3520T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21444301 | |||||||
chrX:21444759 | A | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.519+3978A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21444759 | |||||||
chrX:21444762 | TA | T | 5 | a0001c0001t0002g0006 a0001c0001t0008g0005 a0001c0001t0012g0044 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+3995delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21444762 | ||||||
chrX:21445038 | A | G | 1 | a0001c0001t0023g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.519+4257A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445038 | |||||||
chrX:21445148 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+4367G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445148 | |||||||
chrX:21445413 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+4632C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445413 | |||||||
chrX:21445527 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.519+4746T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445527 | |||||||
chrX:21445635 | A | G | 13 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(10): Show |
13 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+4854A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445635 | |||||||
chrX:21445676 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.519+4895G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445676 | |||||||
chrX:21445772 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.519+4991T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445772 | |||||||
chrX:21446240 | A | G | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.519+5459A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446240 | |||||||
chrX:21446423 | A | G | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+5642A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446423 | |||||||
chrX:21446610 | T | A | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.519+5829T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446610 | |||||||
chrX:21446619 | A | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+5838A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446619 | |||||||
chrX:21446690 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+5909G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446690 | |||||||
chrX:21446901 | T | C | 1 | a0001c0001t0008g0137 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.519+6120T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446901 | |||||||
chrX:21447201 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0028g0002 |
3 | HG02040.hp1 NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.519+6420G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21447201 | |||||||
chrX:21448395 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+7614C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21448395 | |||||||
chrX:21448857 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.519+8076A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21448857 | |||||||
chrX:21449158 | G | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+8377G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21449158 | |||||||
chrX:21449303 | C | CA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0097 others(4): Show |
7 | HG01928.hp1 HG01934.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+8541dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21449303 | ||||||
chrX:21449303 | CA | C | 57 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0002g0003 others(54): Show |
57 | HG00140.hp1 HG00621.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.519+8541delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21449303 | ||||||
chrX:21449841 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+9060C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21449841 | |||||||
chrX:21450033 | C | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+9252C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450033 | |||||||
chrX:21450065 | C | CTG | 8 | a0001c0001t0003g0014 a0001c0001t0003g0024 a0001c0001t0003g0028 others(5): Show |
8 | HG01081.hp1 HG02280.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+9303_519+9304d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21450065 | ||||||
chrX:21450065 | CTG | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+9303_519+9304d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21450065 | ||||||
chrX:21450180 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.519+9399G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450180 | |||||||
chrX:21450717 | G | A | 1 | a0001c0001t0027g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519+9936G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450717 | |||||||
chrX:21450726 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.519+9945C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450726 | |||||||
chrX:21451381 | A | G | 2 | a0001c0001t0006g0154 a0002c0004t0006g0153 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.519+10600A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451381 | |||||||
chrX:21451754 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.519+10973C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451754 | |||||||
chrX:21451795 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.519+11014G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451795 | |||||||
chrX:21451874 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11093G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451874 | |||||||
chrX:21451917 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.519+11136C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451917 | |||||||
chrX:21452157 | C | A | 1 | a0001c0001t0003g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.519+11376C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452157 | |||||||
chrX:21452264 | G | T | 33 | a0001c0001t0001g0157 a0001c0001t0003g0014 a0001c0001t0003g0152 others(30): Show |
33 | HG01071.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.519+11483G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452264 | |||||||
chrX:21452282 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.519+11501C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452282 | |||||||
chrX:21452283 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.519+11502G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452283 | |||||||
chrX:21452290 | C | T | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+11509C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452290 | |||||||
chrX:21452300 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.519+11519A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452300 | |||||||
chrX:21452306 | T | C | 16 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(13): Show |
16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.519+11525T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452306 | |||||||
chrX:21452372 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.519+11591A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452372 | |||||||
chrX:21452578 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.519+11797C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452578 | |||||||
chrX:21452702 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11921G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452702 | |||||||
chrX:21452753 | C | CTTATT | 22 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0157 others(19): Show |
22 | HG00735.hp1 HG01433.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+12035_519+1203 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | C | CTTATTTT others(3): Show |
6 | a0001c0001t0001g0035 a0001c0001t0002g0018 a0001c0001t0002g0112 others(3): Show |
6 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+12030_519+1203 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | C | CTTATTTT others(8): Show |
1 | a0001c0001t0006g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.519+12025_519+1203 others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | C | CTTATTTT others(13): Show |
1 | a0001c0001t0017g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+12020_519+1203 others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | CTTATT | C | 27 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0103 others(24): Show |
27 | HG00609.hp1 HG01071.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.519+12035_519+1203 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | CTTATTTT others(3): Show |
C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0052 others(10): Show |
13 | HG00280.hp1 HG00673.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+12030_519+1203 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | CTTATTTT others(8): Show |
C | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+12025_519+1203 others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452753 | CTTATTTT others(13): Show |
C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0028g0002 |
3 | NA18989.hp1 NA19006.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.519+12020_519+1203 others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | ||||||
chrX:21452756 | A | ATTTTATT others(15): Show |
3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11978_519+1199 others(26): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452756 | ||||||
chrX:21452830 | A | C | 1 | a0001c0001t0005g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.519+12049A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452830 | |||||||
chrX:21453137 | G | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+12356G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453137 | |||||||
chrX:21453394 | TA | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+12615delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21453394 | ||||||
chrX:21453693 | T | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+12912T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453693 | |||||||
chrX:21453859 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+13078G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453859 | |||||||
chrX:21453860 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+13079G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453860 | |||||||
chrX:21454415 | A | G | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.519+13634A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454415 | |||||||
chrX:21454469 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.519+13688C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454469 | |||||||
chrX:21454785 | C | T | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.519+14004C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454785 | |||||||
chrX:21454884 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+14103G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454884 | |||||||
chrX:21455403 | G | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.519+14622G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21455403 | |||||||
chrX:21456017 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-14749C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456017 | |||||||
chrX:21456025 | A | C | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.520-14741A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456025 | |||||||
chrX:21456361 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-14405T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456361 | |||||||
chrX:21456685 | G | C | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-14081G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456685 | |||||||
chrX:21456965 | G | A | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-13801G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456965 | |||||||
chrX:21456968 | A | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520-13798A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456968 | |||||||
chrX:21457110 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-13656T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457110 | |||||||
chrX:21457247 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.520-13519G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457247 | |||||||
chrX:21457508 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-13258T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457508 | |||||||
chrX:21457658 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-13108T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457658 | |||||||
chrX:21457925 | A | G | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.520-12841A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457925 | |||||||
chrX:21458010 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.520-12756G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458010 | |||||||
chrX:21458215 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0140 |
3 | HG02717.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-12551A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458215 | |||||||
chrX:21458426 | G | T | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.520-12340G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458426 | |||||||
chrX:21459018 | C | CT | 8 | a0001c0001t0009g0009 a0001c0001t0009g0011 a0001c0001t0009g0012 others(5): Show |
8 | HG01358.hp1 HG01884.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-11727dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21459018 | ||||||
chrX:21459018 | CT | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG02015.hp1 NA18960.hp1 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-11727delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21459018 | ||||||
chrX:21459108 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.520-11658C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459108 | |||||||
chrX:21459182 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-11584C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459182 | |||||||
chrX:21459213 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-11553A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459213 | |||||||
chrX:21459244 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.520-11522G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459244 | |||||||
chrX:21459375 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.520-11391G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459375 | |||||||
chrX:21459523 | G | T | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-11243G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459523 | |||||||
chrX:21459541 | G | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0008g0124 |
3 | HG00621.hp1 HG02074.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.520-11225G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459541 | |||||||
chrX:21460540 | C | T | 67 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(64): Show |
67 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.520-10226C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460540 | |||||||
chrX:21460672 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-10094C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460672 | |||||||
chrX:21460865 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-9901A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460865 | |||||||
chrX:21461233 | G | A | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-9533G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461233 | |||||||
chrX:21461478 | T | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520-9288T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461478 | |||||||
chrX:21461490 | C | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-9276C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461490 | |||||||
chrX:21461699 | A | G | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-9067A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461699 | |||||||
chrX:21461938 | A | G | 1 | a0001c0001t0023g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.520-8828A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461938 | |||||||
chrX:21462121 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.520-8645G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462121 | |||||||
chrX:21462211 | A | G | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-8555A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462211 | |||||||
chrX:21462714 | A | AT | 42 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0157 others(39): Show |
42 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.520-8035dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21462714 | ||||||
chrX:21462881 | T | G | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.520-7885T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462881 | |||||||
chrX:21462969 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-7797G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462969 | |||||||
chrX:21463001 | C | T | 1 | a0001c0001t0011g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-7765C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463001 | |||||||
chrX:21463313 | G | A | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.520-7453G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463313 | |||||||
chrX:21463807 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.520-6959T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463807 | |||||||
chrX:21464241 | C | G | 41 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(38): Show |
41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.520-6525C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464241 | |||||||
chrX:21464662 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.520-6104G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464662 | |||||||
chrX:21464905 | A | G | 7 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(4): Show |
7 | HG02615.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-5861A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464905 | |||||||
chrX:21465701 | A | G | 1 | a0001c0001t0005g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.520-5065A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21465701 | |||||||
chrX:21466105 | T | A | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-4661T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466105 | |||||||
chrX:21466216 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.520-4550A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466216 | |||||||
chrX:21466286 | A | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-4480A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466286 | |||||||
chrX:21466709 | C | T | 1 | a0001c0001t0006g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.520-4057C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466709 | |||||||
chrX:21467682 | G | GTAAGTTC others(336): Show |
1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-3069_520-3068i others(345): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21467682 | ||||||
chrX:21467954 | T | C | 12 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(9): Show |
12 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-2812T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21467954 | |||||||
chrX:21468059 | A | T | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.520-2707A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468059 | |||||||
chrX:21468078 | T | C | 23 | a0001c0001t0001g0157 a0001c0001t0003g0014 a0001c0001t0006g0154 others(20): Show |
23 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.520-2688T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468078 | |||||||
chrX:21468282 | A | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-2484A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468282 | |||||||
chrX:21468470 | T | G | 1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.520-2296T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468470 | |||||||
chrX:21468716 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(155): Show |
158 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.520-2050T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468716 | |||||||
chrX:21468838 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1928T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468838 | |||||||
chrX:21469108 | ATGTTTAC others(2): Show |
A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1647_520-1639d others(11): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469108 | ||||||
chrX:21469295 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0028g0002 |
2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.520-1471G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469295 | |||||||
chrX:21469479 | A | G | 2 | a0001c0001t0001g0058 a0001c0006t0004g0057 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.520-1287A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469479 | |||||||
chrX:21469626 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1140A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469626 | |||||||
chrX:21469637 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.520-1129G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469637 | |||||||
chrX:21470583 | T | A | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-183T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21470583 | |||||||
chrX:21471039 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+232G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471039 | |||||||
chrX:21471062 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+255T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471062 | |||||||
chrX:21471247 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.561+440T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471247 | |||||||
chrX:21471318 | G | A | 6 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0008g0151 others(3): Show |
6 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+511G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471318 | |||||||
chrX:21471341 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.561+534C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471341 | |||||||
chrX:21471451 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.561+644A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471451 | |||||||
chrX:21471631 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.561+824G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471631 | |||||||
chrX:21471727 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.561+920C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471727 | |||||||
chrX:21471847 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561+1040C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471847 | |||||||
chrX:21471934 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+1127A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471934 | |||||||
chrX:21472021 | C | T | 1 | a0001c0001t0008g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+1214C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472021 | |||||||
chrX:21472129 | G | A | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.561+1322G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472129 | |||||||
chrX:21472382 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+1575T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472382 | |||||||
chrX:21472441 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+1634C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472441 | |||||||
chrX:21472989 | T | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+2182T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472989 | |||||||
chrX:21473745 | G | GT | 12 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0074 others(9): Show |
12 | HG00735.hp2 HG01192.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+2957dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+2944_561+2957d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(12): Show |
4 | a0001c0001t0003g0028 a0001c0001t0036g0136 a0001c0007t0031g0027 others(1): Show |
4 | HG01081.hp1 HG01884.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2939_561+2957d others(21): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(13): Show |
7 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0008g0151 others(4): Show |
7 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(22): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(14): Show |
4 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0010g0160 others(1): Show |
4 | HG02615.hp2 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(23): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0010g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.561+2957_561+2958i others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(16): Show |
5 | a0001c0001t0007g0141 a0001c0001t0009g0010 a0001c0001t0017g0017 others(2): Show |
5 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(25): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(17): Show |
2 | a0001c0001t0009g0011 a0001c0001t0009g0012 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(26): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(19): Show |
2 | a0001c0001t0006g0154 a0001c0001t0006g0156 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(28): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | G | GTTTTTTT others(20): Show |
3 | a0001c0001t0006g0158 a0001c0001t0009g0009 a0001c0001t0034g0008 |
3 | HG02886.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(29): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473745 | GT | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0018 a0001c0001t0005g0021 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+2957delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | ||||||
chrX:21473872 | G | A | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.561+3065G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21473872 | |||||||
chrX:21474526 | A | G | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.561+3719A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21474526 | |||||||
chrX:21475180 | C | T | 1 | a0001c0001t0013g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.561+4373C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475180 | |||||||
chrX:21475319 | A | G | 20 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0024 others(17): Show |
20 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.561+4512A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475319 | |||||||
chrX:21475621 | T | C | 33 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(30): Show |
33 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.561+4814T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475621 | |||||||
chrX:21475967 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+5160T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475967 | |||||||
chrX:21475993 | G | A | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.561+5186G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475993 | |||||||
chrX:21476114 | G | T | 40 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(37): Show |
40 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.561+5307G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476114 | |||||||
chrX:21476272 | A | G | 1 | a0001c0001t0005g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.561+5465A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476272 | |||||||
chrX:21476295 | T | C | 13 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(10): Show |
13 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.561+5488T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476295 | |||||||
chrX:21476493 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561+5686C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476493 | |||||||
chrX:21477067 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.561+6260C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477067 | |||||||
chrX:21477151 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561+6344C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477151 | |||||||
chrX:21477756 | AGGATGTG others(6): Show |
A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+6950_561+6962d others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477756 | |||||||
chrX:21477855 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.561+7048A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477855 | |||||||
chrX:21478624 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.561+7817G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478624 | |||||||
chrX:21478851 | C | T | 40 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(37): Show |
40 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.561+8044C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478851 | |||||||
chrX:21478864 | A | G | 5 | a0001c0001t0022g0032 a0001c0001t0027g0033 a0001c0003t0014g0148 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+8057A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478864 | |||||||
chrX:21478909 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+8102T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478909 | |||||||
chrX:21479101 | A | G | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+8294A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479101 | |||||||
chrX:21479172 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0004g0022 |
2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.561+8365C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479172 | |||||||
chrX:21479772 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+8965A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479772 | |||||||
chrX:21480145 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+9338C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480145 | |||||||
chrX:21480185 | C | T | 1 | a0001c0001t0030g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.561+9378C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480185 | |||||||
chrX:21480276 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0002g0003 a0001c0001t0002g0045 others(20): Show |
23 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.561+9469C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480276 | |||||||
chrX:21480310 | T | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+9503T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480310 | |||||||
chrX:21480427 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.561+9620A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480427 | |||||||
chrX:21480547 | C | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0063 others(13): Show |
16 | HG00673.hp1 HG02040.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.561+9740C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480547 | |||||||
chrX:21481465 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.562-8994C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21481465 | |||||||
chrX:21481493 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.562-8966C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21481493 | |||||||
chrX:21482050 | C | T | 1 | a0001c0001t0032g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.562-8409C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482050 | |||||||
chrX:21482233 | A | G | 12 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(9): Show |
12 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.562-8226A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482233 | |||||||
chrX:21482235 | T | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.562-8224T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482235 | |||||||
chrX:21482318 | A | G | 16 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(13): Show |
16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.562-8141A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482318 | |||||||
chrX:21482383 | A | ACTTGTGC others(4): Show |
18 | a0001c0001t0003g0014 a0001c0001t0007g0141 a0001c0001t0009g0009 others(15): Show |
18 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-8075_562-8074i others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21482383 | ||||||
chrX:21482618 | C | T | 5 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0053 others(2): Show |
5 | HG00609.hp1 HG00741.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-7841C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482618 | |||||||
chrX:21482939 | C | A | 1 | a0001c0001t0002g0049 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.562-7520C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482939 | |||||||
chrX:21483086 | G | A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.562-7373G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483086 | |||||||
chrX:21483117 | G | A | 1 | a0001c0001t0004g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.562-7342G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483117 | |||||||
chrX:21483343 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.562-7116A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483343 | |||||||
chrX:21483593 | A | AAT | 3 | a0001c0001t0001g0001 a0001c0001t0002g0042 a0001c0001t0023g0135 |
3 | HG02809.hp2 HG03654.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.562-6844_562-6843d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | ||||||
chrX:21483593 | A | AATAT | 7 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-6846_562-6843d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | ||||||
chrX:21483593 | AAT | A | 45 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(42): Show |
45 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.562-6844_562-6843d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | ||||||
chrX:21483773 | A | G | 3 | a0001c0001t0003g0082 a0001c0001t0003g0101 a0001c0001t0030g0054 |
3 | NA18967.hp1 NA18994.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.562-6686A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483773 | |||||||
chrX:21483797 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.562-6662C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483797 | |||||||
chrX:21483871 | A | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.562-6588A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483871 | |||||||
chrX:21483899 | C | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-6560C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483899 | |||||||
chrX:21484289 | T | TCAAAA | 3 | a0001c0001t0003g0152 a0001c0001t0004g0072 a0001c0002t0001g0108 |
3 | HG01081.hp2 HG04199.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.562-6134_562-6130d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21484289 | ||||||
chrX:21484289 | TCAAAA | T | 2 | a0001c0001t0001g0052 a0001c0002t0001g0104 |
2 | HG00280.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.562-6134_562-6130d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21484289 | ||||||
chrX:21484331 | C | T | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-6128C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21484331 | |||||||
chrX:21484751 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5708C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21484751 | |||||||
chrX:21485141 | C | G | 1 | a0001c0001t0034g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.562-5318C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485141 | |||||||
chrX:21485166 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5293A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485166 | |||||||
chrX:21485303 | T | C | 4 | a0001c0001t0001g0089 a0001c0001t0004g0088 a0001c0001t0004g0091 others(1): Show |
4 | NA18945.hp1 NA18962.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-5156T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485303 | |||||||
chrX:21485380 | ATGCTC | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5071_562-5067d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21485380 | ||||||
chrX:21485473 | G | A | 1 | a0001c0001t0008g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562-4986G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485473 | |||||||
chrX:21485495 | T | G | 1 | a0001c0001t0002g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.562-4964T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485495 | |||||||
chrX:21485540 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.562-4919G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485540 | |||||||
chrX:21485764 | G | T | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.562-4695G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485764 | |||||||
chrX:21485887 | A | C | 15 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(12): Show |
15 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-4572A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485887 | |||||||
chrX:21485920 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.562-4539A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485920 | |||||||
chrX:21486004 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.562-4455G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486004 | |||||||
chrX:21486016 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.562-4443T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486016 | |||||||
chrX:21486103 | A | G | 41 | a0001c0001t0001g0157 a0001c0001t0002g0026 a0001c0001t0003g0014 others(38): Show |
41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.562-4356A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486103 | |||||||
chrX:21486314 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.562-4145T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486314 | |||||||
chrX:21486719 | T | C | 12 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(9): Show |
12 | HG01071.hp2 HG01243.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.562-3740T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486719 | |||||||
chrX:21486760 | T | C | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.562-3699T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486760 | |||||||
chrX:21486824 | T | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-3635T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486824 | |||||||
chrX:21487026 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-3433C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487026 | |||||||
chrX:21487693 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.562-2766A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487693 | |||||||
chrX:21487715 | G | C | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.562-2744G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487715 | |||||||
chrX:21487715 | G | T | 57 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(54): Show |
57 | HG00140.hp1 HG00621.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.562-2744G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487715 | |||||||
chrX:21488678 | A | G | 1 | a0001c0001t0021g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.562-1781A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21488678 | |||||||
chrX:21488780 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.562-1679G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21488780 | |||||||
chrX:21490384 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0004g0088 a0001c0001t0004g0091 |
3 | NA18945.hp1 NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.562-75G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21490384 | |||||||
chrX:21490616 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.681+38A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21490616 | |||||||
chrX:21490934 | G | T | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.681+356G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21490934 | |||||||
chrX:21492200 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+1622A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21492200 | |||||||
chrX:21492250 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+1672C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21492250 | |||||||
chrX:21492591 | C | CAG | 16 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(13): Show |
16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+2014_681+2015d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21492591 | ||||||
chrX:21493023 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+2445G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493023 | |||||||
chrX:21493146 | T | C | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+2568T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493146 | |||||||
chrX:21493238 | T | G | 1 | a0001c0001t0016g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.681+2660T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493238 | |||||||
chrX:21493386 | A | G | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+2808A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493386 | |||||||
chrX:21493499 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.681+2921A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493499 | |||||||
chrX:21494221 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.682-3566C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21494221 | |||||||
chrX:21495113 | T | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682-2674T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495113 | |||||||
chrX:21495149 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682-2638G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495149 | |||||||
chrX:21495178 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682-2609T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495178 | |||||||
chrX:21495608 | A | AC | 30 | a0001c0001t0001g0058 a0001c0001t0001g0157 a0001c0001t0003g0014 others(27): Show |
30 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.682-2176dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495608 | ||||||
chrX:21495666 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.682-2121C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495666 | |||||||
chrX:21495783 | C | CA | 12 | a0001c0001t0001g0066 a0001c0001t0001g0128 a0001c0001t0001g0131 others(9): Show |
12 | HG01256.hp1 HG01258.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.682-1965dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | C | CAAAAAA | 5 | a0001c0001t0010g0163 a0001c0001t0016g0031 a0001c0001t0017g0017 others(2): Show |
5 | HG01071.hp2 HG02602.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1970_682-1965d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | C | CAAAAAAA | 8 | a0001c0001t0001g0157 a0001c0001t0003g0060 a0001c0001t0005g0117 others(5): Show |
8 | HG02015.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-1971_682-1965d others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | C | CAAAAAAA others(10): Show |
1 | a0002c0004t0006g0153 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-1981_682-1965d others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.682-1989_682-1965d others(27): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0050 others(38): Show |
41 | HG00741.hp1 HG01074.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.682-1965delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAA | C | 17 | a0001c0001t0002g0048 a0001c0001t0002g0112 a0001c0001t0002g0113 others(14): Show |
17 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.682-1966_682-1965d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAA | C | 9 | a0001c0001t0001g0058 a0001c0001t0002g0026 a0001c0001t0002g0111 others(6): Show |
9 | HG01433.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-1967_682-1965d others(5): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0099 a0001c0001t0002g0006 others(2): Show |
5 | HG01071.hp1 HG02135.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1972_682-1965d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.682-1975_682-1965d others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.682-1976_682-1965d others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0006g0154 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-1980_682-1965d others(18): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.682-1981_682-1965d others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0002g0118 others(1): Show |
4 | HG00621.hp1 HG02074.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-1982_682-1965d others(20): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495783 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.682-1983_682-1965d others(21): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | ||||||
chrX:21495822 | A | C | 9 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-1965A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495822 | |||||||
chrX:21495911 | T | C | 17 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(14): Show |
17 | HG01071.hp2 HG01884.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-1876T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495911 | |||||||
chrX:21496492 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0092 a0001c0001t0018g0123 |
3 | HG01358.hp1 HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.682-1295T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21496492 | |||||||
chrX:21496757 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682-1030G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21496757 | |||||||
chrX:21497528 | T | A | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.682-259T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497528 | |||||||
chrX:21497553 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.682-234T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497553 | |||||||
chrX:21497748 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.682-39A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497748 | |||||||
chrX:21497898 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0002g0003 a0001c0001t0002g0045 others(20): Show |
23 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.741+52T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21497898 | |||||||
chrX:21498483 | CT | C | 69 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(66): Show |
69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.741+640delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21498483 | ||||||
chrX:21498530 | A | G | 2 | a0001c0001t0002g0048 a0001c0001t0008g0137 |
2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.741+684A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21498530 | |||||||
chrX:21498815 | A | AT | 11 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(8): Show |
11 | HG01884.hp1 HG02886.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.741+979dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21498815 | ||||||
chrX:21499112 | C | T | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.741+1266C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499112 | |||||||
chrX:21499173 | A | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.741+1327A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499173 | |||||||
chrX:21499902 | A | G | 1 | a0001c0001t0004g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.742-1618A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499902 | |||||||
chrX:21499922 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.742-1598A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499922 | |||||||
chrX:21500554 | A | G | 13 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(10): Show |
13 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-966A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21500554 | |||||||
chrX:21500614 | A | T | 13 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(10): Show |
13 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-906A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21500614 | |||||||
chrX:21501150 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742-370A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501150 | |||||||
chrX:21501205 | T | C | 13 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(10): Show |
13 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-315T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501205 | |||||||
chrX:21501220 | C | T | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.742-300C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501220 | |||||||
chrX:21501314 | TTTTC | T | 3 | a0001c0001t0005g0132 a0001c0001t0016g0031 a0001c0001t0018g0123 |
3 | HG01358.hp1 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.742-200_742-197del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21501314 | ||||||
chrX:21501326 | GTTTA | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.742-189_742-186del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21501326 | ||||||
chrX:21501407 | T | G | 12 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-113T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501407 | |||||||
chrX:21501883 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+295A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21501883 | |||||||
chrX:21502002 | A | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(2): Show |
5 | HG01255.hp1 NA19005.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+414A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502002 | |||||||
chrX:21502286 | T | G | 1 | a0001c0001t0022g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.810+698T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502286 | |||||||
chrX:21502378 | A | G | 4 | a0001c0001t0003g0152 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG01081.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+790A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502378 | |||||||
chrX:21502644 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.810+1056C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502644 | |||||||
chrX:21503554 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+1966A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21503554 | |||||||
chrX:21504658 | G | C | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.810+3070G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21504658 | |||||||
chrX:21504785 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.810+3197T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21504785 | |||||||
chrX:21505640 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.810+4052C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21505640 | |||||||
chrX:21505666 | C | A | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.810+4078C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21505666 | |||||||
chrX:21506222 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.810+4634G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506222 | |||||||
chrX:21506279 | A | G | 1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.810+4691A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506279 | |||||||
chrX:21506439 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.810+4851T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506439 | |||||||
chrX:21506987 | G | GT | 15 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(12): Show |
15 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+5411dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21506987 | ||||||
chrX:21507210 | C | G | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.810+5622C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507210 | |||||||
chrX:21507297 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+5709C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507297 | |||||||
chrX:21507403 | A | T | 16 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(13): Show |
16 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.810+5815A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507403 | |||||||
chrX:21507452 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.810+5864G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507452 | |||||||
chrX:21507562 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.810+5974A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507562 | |||||||
chrX:21507800 | G | A | 16 | a0001c0001t0001g0157 a0001c0001t0003g0152 a0001c0001t0006g0154 others(13): Show |
16 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.810+6212G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507800 | |||||||
chrX:21507832 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+6244A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507832 | |||||||
chrX:21508156 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810+6568C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21508156 | |||||||
chrX:21509026 | T | C | 2 | a0001c0001t0005g0132 a0001c0001t0016g0031 |
2 | HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.810+7438T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509026 | |||||||
chrX:21509052 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.811-7433G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509052 | |||||||
chrX:21509276 | C | G | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-7209C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509276 | |||||||
chrX:21509324 | C | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.811-7161C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509324 | |||||||
chrX:21509495 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.811-6990T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509495 | |||||||
chrX:21510357 | T | TA | 7 | a0001c0001t0002g0026 a0001c0001t0003g0028 a0001c0001t0008g0151 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.811-6119dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21510357 | ||||||
chrX:21511027 | A | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-5458A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511027 | |||||||
chrX:21511099 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-5386C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511099 | |||||||
chrX:21511100 | A | G | 4 | a0001c0001t0035g0007 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-5385A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511100 | |||||||
chrX:21511772 | C | G | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.811-4713C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511772 | |||||||
chrX:21511993 | T | C | 1 | a0003c0005t0003g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.811-4492T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511993 | |||||||
chrX:21512191 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.811-4294A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512191 | |||||||
chrX:21512410 | A | T | 1 | a0001c0001t0004g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.811-4075A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512410 | |||||||
chrX:21512441 | T | C | 4 | a0001c0001t0007g0141 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-4044T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512441 | |||||||
chrX:21512754 | T | TTTTTG | 15 | a0001c0001t0003g0014 a0001c0001t0003g0024 a0001c0001t0009g0009 others(12): Show |
15 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.811-3711_811-3707d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21512754 | ||||||
chrX:21513109 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-3376G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21513109 | |||||||
chrX:21513113 | A | T | 2 | a0001c0001t0009g0010 a0001c0001t0009g0012 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.811-3372A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21513113 | |||||||
chrX:21514403 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.811-2082A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514403 | |||||||
chrX:21514475 | T | C | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.811-2010T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514475 | |||||||
chrX:21514636 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.811-1849T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514636 | |||||||
chrX:21514682 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.811-1803G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514682 | |||||||
chrX:21515041 | T | TA | 5 | a0001c0001t0005g0087 a0001c0001t0035g0007 a0001c0003t0014g0148 others(2): Show |
5 | HG00738.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.811-1433dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21515041 | ||||||
chrX:21515557 | T | A | 8 | a0001c0001t0009g0009 a0001c0001t0010g0160 a0001c0001t0022g0032 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.811-928T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21515557 | |||||||
chrX:21515932 | T | G | 1 | a0001c0001t0005g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.811-553T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21515932 | |||||||
chrX:21516037 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-448G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516037 | |||||||
chrX:21516049 | C | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.811-436C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516049 | |||||||
chrX:21516308 | A | G | 1 | a0001c0001t0005g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.811-177A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516308 | |||||||
chrX:21516391 | A | AC | 22 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0063 others(19): Show |
22 | HG00673.hp1 HG00738.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.811-93dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21516391 | ||||||
chrX:21516943 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+312A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516943 | |||||||
chrX:21516993 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+362A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516993 | |||||||
chrX:21516993 | A | T | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.957+362A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516993 | |||||||
chrX:21517776 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0018g0123 |
2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.957+1145A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21517776 | |||||||
chrX:21517851 | A | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+1220A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21517851 | |||||||
chrX:21518048 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.957+1417T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518048 | |||||||
chrX:21518282 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.957+1651G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518282 | |||||||
chrX:21518339 | C | G | 12 | a0001c0001t0001g0157 a0001c0001t0006g0154 a0001c0001t0006g0156 others(9): Show |
12 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.957+1708C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518339 | |||||||
chrX:21518462 | A | G | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.957+1831A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518462 | |||||||
chrX:21519228 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.957+2597C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519228 | |||||||
chrX:21519390 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.957+2759C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519390 | |||||||
chrX:21519926 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+3295A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519926 | |||||||
chrX:21520405 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+3774C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520405 | |||||||
chrX:21520479 | G | GA | 69 | a0001c0001t0001g0157 a0001c0001t0002g0003 a0001c0001t0002g0006 others(66): Show |
69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.957+3857dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21520479 | ||||||
chrX:21520692 | T | C | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+4061T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520692 | |||||||
chrX:21520923 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+4292A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520923 | |||||||
chrX:21521353 | A | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+4722A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21521353 | |||||||
chrX:21521798 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.958-5069C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21521798 | |||||||
chrX:21522192 | T | C | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-4675T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21522192 | |||||||
chrX:21523741 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.958-3126G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21523741 | |||||||
chrX:21524269 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.958-2598A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524269 | |||||||
chrX:21524502 | G | T | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-2365G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524502 | |||||||
chrX:21524718 | C | G | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.958-2149C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524718 | |||||||
chrX:21525674 | A | G | 2 | a0001c0001t0010g0160 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.958-1193A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21525674 | |||||||
chrX:21525849 | A | C | 1 | a0001c0001t0003g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.958-1018A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21525849 | |||||||
chrX:21526206 | T | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0028g0002 |
3 | NA18989.hp1 NA19006.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.958-661T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526206 | |||||||
chrX:21526660 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.958-207C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526660 | |||||||
chrX:21526766 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.958-101T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526766 | |||||||
chrX:21526786 | A | ATTG | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0010g0160 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-51_958-49dupGT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526786 | ||||||
chrX:21526786 | ATTG | A | 5 | a0001c0001t0003g0030 a0001c0001t0017g0017 a0001c0003t0014g0148 others(2): Show |
5 | HG01071.hp2 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-51_958-49delGT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526786 | ||||||
chrX:21527227 | ATC | A | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1091+230_1091+231d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21527227 | ||||||
chrX:21527230 | T | C | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1091+230T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527230 | |||||||
chrX:21527370 | A | T | 5 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+370A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527370 | |||||||
chrX:21527617 | T | C | 1 | a0001c0001t0004g0088 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1091+617T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527617 | |||||||
chrX:21527624 | A | T | 4 | a0001c0001t0035g0007 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+624A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527624 | |||||||
chrX:21527806 | ATAATT | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(18): Show |
21 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1091+810_1091+814d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21527806 | ||||||
chrX:21527852 | C | A | 1 | a0001c0001t0011g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091+852C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527852 | |||||||
chrX:21527872 | A | G | 5 | a0001c0001t0010g0160 a0001c0001t0035g0007 a0001c0003t0014g0148 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+872A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527872 | |||||||
chrX:21528002 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0030 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1091+1002A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528002 | |||||||
chrX:21528049 | T | C | 16 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(13): Show |
16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+1049T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528049 | |||||||
chrX:21528259 | A | G | 1 | a0001c0001t0005g0053 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1091+1259A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528259 | |||||||
chrX:21528865 | C | G | 4 | a0001c0001t0002g0115 a0001c0001t0003g0082 a0001c0001t0003g0101 others(1): Show |
4 | NA18967.hp1 NA18974.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+1865C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528865 | |||||||
chrX:21528937 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1091+1937T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528937 | |||||||
chrX:21529017 | T | C | 6 | a0001c0001t0002g0018 a0001c0001t0010g0160 a0001c0001t0035g0007 others(3): Show |
6 | HG01106.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091+2017T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529017 | |||||||
chrX:21529328 | A | G | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1091+2328A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529328 | |||||||
chrX:21529405 | A | G | 2 | a0001c0001t0010g0160 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1091+2405A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529405 | |||||||
chrX:21529659 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1092-2197A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529659 | |||||||
chrX:21530465 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1092-1391C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21530465 | |||||||
chrX:21532887 | A | G | 4 | a0001c0001t0001g0089 a0001c0001t0004g0088 a0001c0001t0004g0091 others(1): Show |
4 | NA18945.hp1 NA18962.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+820A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21532887 | |||||||
chrX:21533383 | A | G | 5 | a0001c0001t0010g0160 a0001c0001t0035g0007 a0001c0003t0014g0148 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+1316A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533383 | |||||||
chrX:21533463 | A | T | 1 | a0001c0002t0007g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1303+1396A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533463 | |||||||
chrX:21533659 | A | G | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303+1592A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533659 | |||||||
chrX:21533824 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1303+1757A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533824 | |||||||
chrX:21534068 | A | G | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1303+2001A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534068 | |||||||
chrX:21534117 | G | GT | 2 | a0001c0001t0010g0160 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303+2051dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21534117 | ||||||
chrX:21534123 | A | G | 14 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(11): Show |
14 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303+2056A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534123 | |||||||
chrX:21534295 | G | A | 5 | a0001c0001t0010g0160 a0001c0001t0035g0007 a0001c0003t0014g0148 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+2228G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534295 | |||||||
chrX:21534295 | G | GAT | 2 | a0001c0001t0001g0092 a0001c0001t0018g0123 |
2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1303+2241_1303+224 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21534295 | ||||||
chrX:21534410 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+2343T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534410 | |||||||
chrX:21534418 | A | G | 12 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(9): Show |
12 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303+2351A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534418 | |||||||
chrX:21534734 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+2667T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534734 | |||||||
chrX:21534739 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1303+2672C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534739 | |||||||
chrX:21534966 | C | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1303+2899C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534966 | |||||||
chrX:21535389 | A | AT | 9 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(6): Show |
9 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303+3330dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21535389 | ||||||
chrX:21535514 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+3447A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21535514 | |||||||
chrX:21536116 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1303+4049A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21536116 | |||||||
chrX:21536829 | G | GT | 19 | a0001c0001t0002g0115 a0001c0001t0003g0014 a0001c0001t0003g0082 others(16): Show |
19 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1303+4776dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21536829 | ||||||
chrX:21537255 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1303+5188T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537255 | |||||||
chrX:21537399 | TAA | T | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1303+5333_1303+533 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537399 | |||||||
chrX:21537731 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0002g0018 a0001c0001t0004g0088 others(2): Show |
5 | HG01106.hp1 NA18945.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+5664G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537731 | |||||||
chrX:21537786 | GT | G | 5 | a0001c0001t0001g0073 a0001c0001t0002g0046 a0001c0001t0004g0069 others(2): Show |
5 | HG02647.hp1 HG03710.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+5735delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21537786 | ||||||
chrX:21537793 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1303+5726T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537793 | |||||||
chrX:21537804 | T | G | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+5737T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537804 | |||||||
chrX:21538124 | A | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+6057A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21538124 | |||||||
chrX:21538229 | T | G | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+6162T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21538229 | |||||||
chrX:21539502 | G | GT | 34 | a0001c0001t0001g0157 a0001c0001t0003g0014 a0001c0001t0006g0154 others(31): Show |
34 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1303+7444dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21539502 | ||||||
chrX:21539596 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1303+7529A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21539596 | |||||||
chrX:21540073 | A | T | 1 | a0001c0001t0005g0053 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1303+8006A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540073 | |||||||
chrX:21540077 | A | G | 1 | a0001c0001t0005g0053 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1303+8010A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540077 | |||||||
chrX:21540141 | G | T | 1 | a0001c0001t0007g0020 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1303+8074G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540141 | |||||||
chrX:21540311 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1303+8244G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540311 | |||||||
chrX:21540460 | G | T | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1303+8393G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540460 | |||||||
chrX:21540659 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1303+8592A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540659 | |||||||
chrX:21540970 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0004g0072 |
3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1303+8903A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540970 | |||||||
chrX:21541046 | G | A | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+8979G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541046 | |||||||
chrX:21541076 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1303+9009G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541076 | |||||||
chrX:21541132 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1303+9065G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541132 | |||||||
chrX:21541583 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0002g0118 others(1): Show |
4 | HG00621.hp1 HG02074.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+9516A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541583 | |||||||
chrX:21541617 | C | A | 3 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0055 |
3 | HG00741.hp1 HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1303+9550C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541617 | |||||||
chrX:21542249 | G | T | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303+10182G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542249 | |||||||
chrX:21542384 | G | A | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1303+10317G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542384 | |||||||
chrX:21542515 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+10448A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542515 | |||||||
chrX:21542729 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1303+10662G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542729 | |||||||
chrX:21542937 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1303+10870T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542937 | |||||||
chrX:21543057 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+10990A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543057 | |||||||
chrX:21543336 | G | A | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+11269G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543336 | |||||||
chrX:21543492 | G | A | 1 | a0001c0003t0014g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1303+11425G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543492 | |||||||
chrX:21544172 | A | G | 3 | a0001c0001t0003g0043 a0001c0001t0029g0079 a0001c0001t0032g0085 |
3 | HG02735.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1303+12105A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544172 | |||||||
chrX:21544316 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1303+12249G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544316 | |||||||
chrX:21544480 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+12413T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544480 | |||||||
chrX:21544486 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1303+12419G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544486 | |||||||
chrX:21544555 | G | C | 7 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(4): Show |
7 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303+12488G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544555 | |||||||
chrX:21544586 | T | C | 1 | a0001c0001t0016g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1303+12519T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544586 | |||||||
chrX:21544792 | G | A | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1303+12725G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544792 | |||||||
chrX:21544830 | A | G | 2 | a0001c0001t0010g0160 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303+12763A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544830 | |||||||
chrX:21544909 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1303+12842C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544909 | |||||||
chrX:21545815 | G | C | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1303+13748G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21545815 | |||||||
chrX:21546014 | T | G | 1 | a0001c0001t0034g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1303+13947T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546014 | |||||||
chrX:21546063 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1303+13996G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546063 | |||||||
chrX:21546438 | C | T | 27 | a0001c0001t0003g0014 a0001c0001t0006g0154 a0001c0001t0006g0156 others(24): Show |
27 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1303+14371C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546438 | |||||||
chrX:21546655 | A | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0004g0072 |
3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1303+14588A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546655 | |||||||
chrX:21546767 | G | C | 7 | a0001c0001t0010g0160 a0001c0001t0022g0032 a0001c0001t0027g0033 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+14700G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546767 | |||||||
chrX:21546895 | T | C | 2 | a0001c0001t0010g0160 a0001c0001t0035g0007 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1304-14576T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546895 | |||||||
chrX:21547323 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1304-14148A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547323 | |||||||
chrX:21547365 | A | T | 1 | a0001c0001t0010g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1304-14106A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547365 | |||||||
chrX:21547366 | C | T | 1 | a0001c0001t0010g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1304-14105C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547366 | |||||||
chrX:21547847 | T | G | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1304-13624T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547847 | |||||||
chrX:21547914 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1304-13557G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547914 | |||||||
chrX:21548053 | G | A | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1304-13418G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548053 | |||||||
chrX:21548133 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-13338A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548133 | |||||||
chrX:21548493 | C | G | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1304-12978C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548493 | |||||||
chrX:21548784 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1304-12687C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548784 | |||||||
chrX:21549026 | C | G | 12 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(9): Show |
12 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1304-12445C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549026 | |||||||
chrX:21549324 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1304-12147A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549324 | |||||||
chrX:21549520 | C | T | 2 | a0001c0001t0006g0154 a0002c0004t0006g0153 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1304-11951C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549520 | |||||||
chrX:21549672 | A | G | 26 | a0001c0001t0003g0014 a0001c0001t0006g0154 a0001c0001t0006g0156 others(23): Show |
26 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1304-11799A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549672 | |||||||
chrX:21549813 | T | C | 14 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(11): Show |
14 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1304-11658T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549813 | |||||||
chrX:21550233 | G | A | 32 | a0001c0001t0003g0014 a0001c0001t0006g0154 a0001c0001t0006g0156 others(29): Show |
32 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1304-11238G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550233 | |||||||
chrX:21550362 | G | A | 2 | a0001c0001t0005g0129 a0001c0001t0013g0061 |
2 | HG00609.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1304-11109G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550362 | |||||||
chrX:21550618 | G | A | 1 | a0001c0001t0005g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1304-10853G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550618 | |||||||
chrX:21550971 | G | C | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1304-10500G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550971 | |||||||
chrX:21551030 | CA | C | 26 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(23): Show |
26 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1304-10426delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21551030 | ||||||
chrX:21551218 | G | A | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304-10253G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551218 | |||||||
chrX:21551322 | A | T | 1 | a0001c0001t0034g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1304-10149A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551322 | |||||||
chrX:21551369 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1304-10102G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551369 | |||||||
chrX:21551505 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(18): Show |
21 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1304-9966G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551505 | |||||||
chrX:21551802 | A | G | 22 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0063 others(19): Show |
22 | HG00673.hp1 HG00738.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1304-9669A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551802 | |||||||
chrX:21551948 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0099 others(1): Show |
4 | HG02040.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-9523A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551948 | |||||||
chrX:21552099 | GA | G | 5 | a0001c0001t0001g0131 a0001c0001t0011g0015 a0001c0003t0014g0148 others(2): Show |
5 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304-9358delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21552099 | ||||||
chrX:21552212 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0028g0002 |
2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1304-9259G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552212 | |||||||
chrX:21552598 | A | C | 4 | a0001c0001t0019g0013 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-8873A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552598 | |||||||
chrX:21552617 | G | A | 5 | a0001c0001t0007g0020 a0001c0001t0035g0007 a0001c0003t0014g0148 others(2): Show |
5 | HG02132.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304-8854G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552617 | |||||||
chrX:21552875 | G | A | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1304-8596G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552875 | |||||||
chrX:21553215 | T | G | 1 | a0001c0001t0004g0022 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1304-8256T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553215 | |||||||
chrX:21553479 | CT | C | 8 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304-7991delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553479 | |||||||
chrX:21553497 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-7974G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553497 | |||||||
chrX:21553534 | CA | C | 11 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1304-7924delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553534 | ||||||
chrX:21553571 | A | G | 1 | a0001c0001t0013g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1304-7900A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553571 | |||||||
chrX:21553691 | CT | C | 4 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-7778delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553691 | ||||||
chrX:21554478 | C | T | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1304-6993C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21554478 | |||||||
chrX:21554782 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0037 others(32): Show |
35 | HG00642.hp1 HG01255.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.1304-6689T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21554782 | |||||||
chrX:21555400 | C | G | 17 | a0001c0001t0003g0014 a0001c0001t0009g0009 a0001c0001t0009g0010 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1304-6071C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555400 | |||||||
chrX:21555424 | C | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1304-6047C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555424 | |||||||
chrX:21555443 | A | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1304-6028A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555443 | |||||||
chrX:21555457 | T | C | 1 | a0001c0001t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1304-6014T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555457 | |||||||
chrX:21557645 | G | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0018 others(66): Show |
69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1304-3826G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557645 | |||||||
chrX:21557758 | T | A | 4 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-3713T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557758 | |||||||
chrX:21557818 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-3653T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557818 | |||||||
chrX:21557943 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1304-3528G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557943 | |||||||
chrX:21558103 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-3368C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558103 | |||||||
chrX:21558381 | T | A | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1304-3090T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558381 | |||||||
chrX:21558677 | T | G | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1304-2794T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558677 | |||||||
chrX:21559112 | G | A | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1304-2359G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559112 | |||||||
chrX:21559255 | A | G | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1304-2216A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559255 | |||||||
chrX:21559302 | T | C | 7 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1304-2169T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559302 | |||||||
chrX:21559520 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-1951A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559520 | |||||||
chrX:21559523 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-1948G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559523 | |||||||
chrX:21559668 | T | G | 6 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-1803T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559668 | |||||||
chrX:21560241 | G | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-1230G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560241 | |||||||
chrX:21560380 | A | G | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1304-1091A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560380 | |||||||
chrX:21560403 | C | T | 1 | a0001c0001t0010g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1304-1068C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560403 | |||||||
chrX:21560883 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-588T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560883 | |||||||
chrX:21561167 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1304-304T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21561167 | |||||||
chrX:21561182 | TA | T | 35 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0103 others(32): Show |
35 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1304-271delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | ||||||
chrX:21561182 | TAA | T | 28 | a0001c0001t0002g0018 a0001c0001t0003g0014 a0001c0001t0005g0129 others(25): Show |
28 | HG00609.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1304-272_1304-271d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | ||||||
chrX:21561270 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG03491.hp1 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1304-201C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21561270 | |||||||
chrX:21562003 | T | G | 1 | a0001c0001t0006g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1393+443T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562003 | |||||||
chrX:21562028 | G | GA | 6 | a0001c0001t0002g0111 a0001c0001t0006g0154 a0001c0001t0007g0141 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1393+480dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21562028 | ||||||
chrX:21562268 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1393+708A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562268 | |||||||
chrX:21562365 | G | A | 1 | a0001c0006t0004g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1393+805G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562365 | |||||||
chrX:21562718 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1394-520A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562718 | |||||||
chrX:21563158 | C | CTAA | 7 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394-77_1394-75dup others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21563158 | ||||||
chrX:21563663 | T | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0056 others(3): Show |
6 | HG02056.hp1 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+211T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21563663 | |||||||
chrX:21564178 | A | G | 70 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0018 others(67): Show |
70 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1608+726A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564178 | |||||||
chrX:21564206 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+754G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564206 | |||||||
chrX:21564231 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+779G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564231 | |||||||
chrX:21564381 | A | G | 4 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0005g0019 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+929A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564381 | |||||||
chrX:21564454 | A | C | 1 | a0001c0001t0015g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1608+1002A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564454 | |||||||
chrX:21564754 | GT | G | 25 | a0001c0001t0003g0014 a0001c0001t0006g0154 a0001c0001t0006g0156 others(22): Show |
25 | HG01081.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1608+1313delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564754 | ||||||
chrX:21565123 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1608+1671C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565123 | |||||||
chrX:21565371 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0005g0019 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1608+1919G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565371 | |||||||
chrX:21565608 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+2156T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565608 | |||||||
chrX:21566099 | A | AT | 36 | a0001c0001t0002g0006 a0001c0001t0003g0014 a0001c0001t0003g0030 others(33): Show |
36 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1608+2650dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21566099 | ||||||
chrX:21566145 | G | A | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1608+2693G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566145 | |||||||
chrX:21566169 | A | T | 3 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0071 |
3 | NA18747.hp1 NA18960.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1608+2717A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566169 | |||||||
chrX:21566263 | G | C | 4 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+2811G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566263 | |||||||
chrX:21566499 | T | G | 2 | a0001c0001t0009g0011 a0001c0001t0034g0008 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1608+3047T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566499 | |||||||
chrX:21567067 | G | T | 1 | a0001c0001t0012g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1608+3615G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567067 | |||||||
chrX:21567359 | T | C | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1608+3907T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567359 | |||||||
chrX:21567795 | G | GGTGT | 4 | a0001c0001t0001g0073 a0001c0001t0004g0072 a0001c0001t0009g0009 others(1): Show |
4 | HG01884.hp2 HG03486.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+4386_1608+438 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0011g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1608+4380_1608+438 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | G | GGTT | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+4345_1608+434 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | GGT | G | 29 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0001g0097 others(26): Show |
29 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1608+4388_1608+438 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | GGTGT | G | 57 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(54): Show |
57 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1608+4386_1608+438 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | GGTGTGT | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0051 others(31): Show |
34 | HG00642.hp1 HG01255.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1608+4384_1608+438 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0002g0018 a0001c0001t0002g0111 a0001c0001t0002g0112 others(4): Show |
7 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+4382_1608+438 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567795 | GGTGTGTG others(3): Show |
G | 8 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0101 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+4380_1608+438 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | ||||||
chrX:21567891 | T | C | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1608+4439T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567891 | |||||||
chrX:21567899 | A | T | 1 | a0001c0001t0010g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1608+4447A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567899 | |||||||
chrX:21567922 | T | C | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1608+4470T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567922 | |||||||
chrX:21568205 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1608+4753T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568205 | |||||||
chrX:21568351 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1608+4899C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568351 | |||||||
chrX:21568585 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1608+5133G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568585 | |||||||
chrX:21569114 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+5662T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569114 | |||||||
chrX:21569210 | G | GTTA | 4 | a0001c0001t0035g0007 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+5779_1608+578 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21569210 | ||||||
chrX:21569218 | T | G | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1608+5766T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569218 | |||||||
chrX:21569508 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1608+6056C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569508 | |||||||
chrX:21569515 | A | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+6063A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569515 | |||||||
chrX:21570271 | C | G | 1 | a0001c0001t0016g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1608+6819C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570271 | |||||||
chrX:21570706 | G | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+7254G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570706 | |||||||
chrX:21570767 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1608+7315C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570767 | |||||||
chrX:21570974 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+7522T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570974 | |||||||
chrX:21571313 | A | G | 1 | a0001c0001t0008g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1608+7861A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571313 | |||||||
chrX:21571467 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+8015A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571467 | |||||||
chrX:21571684 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1608+8232A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571684 | |||||||
chrX:21572131 | A | G | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1608+8679A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572131 | |||||||
chrX:21572329 | A | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+8877A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572329 | |||||||
chrX:21572624 | C | G | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+9172C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572624 | |||||||
chrX:21572792 | A | G | 11 | a0001c0001t0003g0030 a0001c0001t0006g0156 a0001c0001t0006g0158 others(8): Show |
11 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1608+9340A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572792 | |||||||
chrX:21573050 | C | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | NA18984.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1608+9598C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573050 | |||||||
chrX:21573436 | C | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+9984C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573436 | |||||||
chrX:21573497 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1608+10045G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573497 | |||||||
chrX:21574555 | G | T | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+11103G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21574555 | |||||||
chrX:21574764 | G | A | 11 | a0001c0001t0006g0156 a0001c0001t0006g0158 a0001c0001t0006g0159 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1608+11312G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21574764 | |||||||
chrX:21575222 | A | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1608+11770A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575222 | |||||||
chrX:21575279 | T | C | 1 | a0001c0002t0007g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1608+11827T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575279 | |||||||
chrX:21575518 | A | G | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1608+12066A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575518 | |||||||
chrX:21575523 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+12071T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575523 | |||||||
chrX:21575968 | C | G | 2 | a0001c0001t0007g0141 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1608+12516C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575968 | |||||||
chrX:21576268 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1608+12816G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576268 | |||||||
chrX:21576753 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1608+13301G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576753 | |||||||
chrX:21576876 | T | C | 3 | a0001c0003t0014g0148 a0001c0003t0014g0149 a0001c0003t0026g0150 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+13424T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576876 | |||||||
chrX:21577112 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0157 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1609-13460C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21577112 | |||||||
chrX:21577139 | A | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-13433A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21577139 | |||||||
chrX:21578370 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1609-12202A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21578370 | |||||||
chrX:21578549 | G | GT | 12 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0064 others(9): Show |
12 | HG00280.hp1 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-12007dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | ||||||
chrX:21578549 | GT | G | 27 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0063 others(24): Show |
27 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1609-12007delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | ||||||
chrX:21578930 | G | A | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1609-11642G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21578930 | |||||||
chrX:21579718 | G | C | 8 | a0001c0001t0002g0026 a0001c0001t0003g0024 a0001c0001t0003g0028 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-10854G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21579718 | |||||||
chrX:21581004 | C | T | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1609-9568C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581004 | |||||||
chrX:21581245 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-9327T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581245 | |||||||
chrX:21581521 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1609-9051G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581521 | |||||||
chrX:21581657 | A | G | 4 | a0001c0001t0035g0007 a0001c0003t0014g0148 a0001c0003t0014g0149 others(1): Show |
4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-8915A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581657 | |||||||
chrX:21581770 | T | C | 5 | a0001c0001t0003g0014 a0001c0001t0011g0015 a0001c0001t0011g0016 others(2): Show |
5 | HG02717.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609-8802T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581770 | |||||||
chrX:21582396 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-8176T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21582396 | |||||||
chrX:21582958 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1609-7614T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21582958 | |||||||
chrX:21583313 | T | C | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-7259T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21583313 | |||||||
chrX:21584360 | T | C | 1 | a0001c0001t0007g0020 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1609-6212T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21584360 | |||||||
chrX:21584933 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1609-5639C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21584933 | |||||||
chrX:21585621 | G | A | 1 | a0001c0001t0004g0069 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1609-4951G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585621 | |||||||
chrX:21585667 | T | G | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-4905T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585667 | |||||||
chrX:21585707 | T | C | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-4865T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585707 | |||||||
chrX:21586185 | G | C | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1609-4387G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586185 | |||||||
chrX:21586251 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1609-4321G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586251 | |||||||
chrX:21586332 | G | T | 2 | a0001c0001t0002g0111 a0001c0001t0013g0061 |
2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1609-4240G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586332 | |||||||
chrX:21586413 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1609-4159G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586413 | |||||||
chrX:21586472 | G | T | 1 | a0001c0001t0013g0061 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1609-4100G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586472 | |||||||
chrX:21586847 | C | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-3725C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586847 | |||||||
chrX:21586877 | G | C | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-3695G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586877 | |||||||
chrX:21586904 | G | A | 4 | a0001c0001t0002g0115 a0001c0001t0003g0082 a0001c0001t0003g0101 others(1): Show |
4 | NA18967.hp1 NA18974.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-3668G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586904 | |||||||
chrX:21587111 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1609-3461C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587111 | |||||||
chrX:21587156 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0099 others(1): Show |
4 | HG02040.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-3416T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587156 | |||||||
chrX:21587493 | T | C | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1609-3079T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587493 | |||||||
chrX:21587597 | T | G | 5 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 others(2): Show |
5 | HG01071.hp2 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-2975T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587597 | |||||||
chrX:21587943 | G | A | 3 | a0001c0001t0002g0115 a0001c0001t0003g0082 a0001c0001t0030g0054 |
3 | NA18967.hp1 NA18974.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1609-2629G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587943 | |||||||
chrX:21588844 | A | G | 6 | a0001c0001t0003g0028 a0001c0001t0007g0141 a0001c0001t0010g0160 others(3): Show |
6 | HG01071.hp2 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1728A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21588844 | |||||||
chrX:21589168 | A | G | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1404A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589168 | |||||||
chrX:21589685 | A | G | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-887A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589685 | |||||||
chrX:21589777 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1609-795C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589777 | |||||||
chrX:21590503 | G | A | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-69G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21590503 | |||||||
chrX:21591383 | T | TTG | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1830+189_1830+190i others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591383 | |||||||
chrX:21591384 | A | T | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1830+190A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591384 | |||||||
chrX:21591558 | G | T | 1 | a0001c0001t0003g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1830+364G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591558 | |||||||
chrX:21591704 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1830+510C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591704 | |||||||
chrX:21591710 | G | T | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1830+516G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591710 | |||||||
chrX:21591728 | A | G | 6 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1830+534A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591728 | |||||||
chrX:21592027 | A | G | 29 | a0001c0001t0003g0028 a0001c0001t0006g0154 a0001c0001t0006g0156 others(26): Show |
29 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1830+833A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21592027 | |||||||
chrX:21592775 | A | T | 2 | a0001c0001t0002g0111 a0001c0001t0013g0061 |
2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1830+1581A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21592775 | |||||||
chrX:21593184 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1831-1790A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593184 | |||||||
chrX:21593772 | G | A | 7 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-1202G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593772 | |||||||
chrX:21593914 | C | T | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1831-1060C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593914 | |||||||
chrX:21594025 | A | T | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1831-949A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21594025 | |||||||
chrX:21594117 | T | C | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1831-857T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21594117 | |||||||
chrX:21595478 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1976+83C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595478 | |||||||
chrX:21595555 | A | G | 2 | a0001c0001t0028g0002 a0001c0002t0007g0039 |
2 | NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1976+160A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595555 | |||||||
chrX:21595746 | C | T | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1976+351C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595746 | |||||||
chrX:21595902 | C | CA | 2 | a0001c0001t0009g0010 a0001c0001t0009g0012 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1976+508dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21595902 | ||||||
chrX:21596120 | T | C | 1 | a0001c0001t0027g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1976+725T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596120 | |||||||
chrX:21596264 | G | A | 3 | a0001c0001t0006g0156 a0001c0001t0006g0158 a0001c0006t0004g0057 |
3 | HG02886.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1976+869G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596264 | |||||||
chrX:21596503 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1976+1108T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596503 | |||||||
chrX:21597015 | G | A | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976+1620G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597015 | |||||||
chrX:21597033 | C | A | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1976+1638C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597033 | |||||||
chrX:21597404 | T | G | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976+2009T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597404 | |||||||
chrX:21598008 | C | CAT | 3 | a0001c0001t0001g0035 a0001c0001t0020g0142 a0001c0001t0035g0007 |
3 | HG01243.hp1 HG02647.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1976+2631_1976+263 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | ||||||
chrX:21598008 | C | CATAT | 3 | a0001c0001t0001g0075 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG02615.hp1 HG03471.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1976+2629_1976+263 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | ||||||
chrX:21598008 | CAT | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0007g0090 others(4): Show |
7 | HG00673.hp1 HG01109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1976+2631_1976+263 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | ||||||
chrX:21598025 | A | G | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1976+2630A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598025 | |||||||
chrX:21598042 | C | A | 2 | a0001c0001t0011g0015 a0001c0001t0011g0140 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1976+2647C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598042 | |||||||
chrX:21598242 | G | C | 30 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(27): Show |
30 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1976+2847G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598242 | |||||||
chrX:21598252 | A | G | 6 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 others(3): Show |
6 | NA18943.hp1 NA18944.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1976+2857A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598252 | |||||||
chrX:21598356 | G | GA | 3 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1977-2925dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598356 | ||||||
chrX:21598969 | C | T | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1977-2313C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598969 | |||||||
chrX:21598974 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1977-2308T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598974 | |||||||
chrX:21599339 | G | GGT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0157 others(12): Show |
15 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1977-1899_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | ||||||
chrX:21599339 | G | GGTGT | 3 | a0001c0001t0002g0042 a0001c0001t0002g0125 a0001c0001t0035g0007 |
3 | HG02647.hp1 HG02809.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1977-1901_1977-189 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | ||||||
chrX:21599339 | GGT | G | 61 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(58): Show |
61 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1977-1899_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | ||||||
chrX:21599339 | GGTGT | G | 38 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0063 others(35): Show |
38 | HG00280.hp1 HG00673.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1977-1901_1977-189 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | ||||||
chrX:21599339 | GGTGTGT | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0005g0129 others(1): Show |
4 | HG00609.hp1 HG02486.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1977-1903_1977-189 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | ||||||
chrX:21599348 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1977-1934G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21599348 | |||||||
chrX:21599383 | TGA | T | 6 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0003g0024 others(3): Show |
6 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1977-1896_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599383 | ||||||
chrX:21599896 | A | G | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1977-1386A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21599896 | |||||||
chrX:21600039 | A | C | 2 | a0001c0001t0012g0044 a0001c0001t0020g0142 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1977-1243A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600039 | |||||||
chrX:21600112 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0067 |
3 | HG00642.hp1 HG01261.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.1977-1170C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600112 | |||||||
chrX:21600427 | C | T | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1977-855C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600427 | |||||||
chrX:21600880 | C | T | 1 | a0001c0001t0017g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1977-402C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600880 | |||||||
chrX:21601949 | G | A | 3 | a0001c0001t0011g0015 a0001c0001t0011g0016 a0001c0001t0011g0140 |
3 | HG03041.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2044+600G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21601949 | |||||||
chrX:21602129 | G | T | 7 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(4): Show |
7 | HG01071.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044+780G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602129 | |||||||
chrX:21602164 | C | T | 1 | a0001c0003t0014g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2044+815C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602164 | |||||||
chrX:21602194 | G | A | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2044+845G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602194 | |||||||
chrX:21602229 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0004g0022 |
2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2044+880C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602229 | |||||||
chrX:21602504 | A | C | 3 | a0001c0001t0011g0015 a0001c0001t0011g0016 a0001c0001t0011g0140 |
3 | HG03041.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2044+1155A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602504 | |||||||
chrX:21602736 | G | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0004g0072 |
3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2044+1387G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602736 | |||||||
chrX:21602939 | C | G | 8 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0003g0024 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044+1590C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602939 | |||||||
chrX:21603100 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2044+1751A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603100 | |||||||
chrX:21603372 | C | A | 6 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(3): Show |
6 | HG02615.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044+2023C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603372 | |||||||
chrX:21603400 | A | G | 1 | a0001c0001t0003g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2044+2051A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603400 | |||||||
chrX:21604030 | G | A | 4 | a0001c0001t0011g0015 a0001c0001t0011g0016 a0001c0001t0011g0140 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044+2681G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21604030 | |||||||
chrX:21604470 | A | AAT | 5 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 others(2): Show |
5 | HG01071.hp2 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-2299_2045-229 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 21604470 | ||||||
chrX:21605313 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0128 |
2 | NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2045-1466A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605313 | |||||||
chrX:21605357 | T | C | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2045-1422T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605357 | |||||||
chrX:21605515 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2045-1264A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605515 | |||||||
chrX:21605639 | A | G | 7 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2045-1140A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605639 | |||||||
chrX:21605646 | TC | T | 3 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0071 |
3 | NA18747.hp1 NA18960.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2045-1132delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605646 | |||||||
chrX:21605754 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2045-1025G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605754 | |||||||
chrX:21605769 | C | T | 9 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0003g0024 others(6): Show |
9 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2045-1010C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605769 | |||||||
chrX:21605882 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2045-897A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605882 | |||||||
chrX:21605982 | T | C | 3 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2045-797T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605982 | |||||||
chrX:21606228 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2045-551G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21606228 | |||||||
chrX:21606430 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2045-349A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21606430 | |||||||
chrX:21607315 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2145+436G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21607315 | |||||||
chrX:21608603 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2146-468T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608603 | |||||||
chrX:21608624 | T | C | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2146-447T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608624 | |||||||
chrX:21608740 | T | G | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2146-331T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608740 | |||||||
chrX:21609807 | T | C | 1 | a0001c0001t0023g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2692+190T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609807 | |||||||
chrX:21609852 | T | G | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+235T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609852 | |||||||
chrX:21609973 | G | A | 1 | a0001c0001t0017g0017 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2692+356G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609973 | |||||||
chrX:21610138 | G | A | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2692+521G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610138 | |||||||
chrX:21610250 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2692+633C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610250 | |||||||
chrX:21610334 | T | C | 9 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(6): Show |
9 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+717T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610334 | |||||||
chrX:21611299 | T | A | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2692+1682T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611299 | |||||||
chrX:21611697 | G | C | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+2080G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611697 | |||||||
chrX:21611739 | C | A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+2122C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611739 | |||||||
chrX:21611893 | ACT | A | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2692+2277_2692+227 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611893 | |||||||
chrX:21612694 | G | C | 2 | a0001c0001t0023g0135 a0001c0001t0036g0136 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2692+3077G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21612694 | |||||||
chrX:21613484 | C | T | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2692+3867C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21613484 | |||||||
chrX:21613939 | C | CA | 5 | a0001c0001t0002g0114 a0001c0001t0011g0015 a0001c0001t0011g0016 others(2): Show |
5 | HG00140.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2692+4336dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21613939 | ||||||
chrX:21614121 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2692+4504G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614121 | |||||||
chrX:21614585 | T | TA | 23 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0006g0154 others(20): Show |
23 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2692+4976dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21614585 | ||||||
chrX:21614712 | G | T | 1 | a0001c0001t0022g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2692+5095G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614712 | |||||||
chrX:21614716 | G | C | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+5099G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614716 | |||||||
chrX:21615253 | T | A | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2692+5636T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615253 | |||||||
chrX:21615521 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2692+5904T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615521 | |||||||
chrX:21615561 | A | G | 4 | a0001c0001t0011g0015 a0001c0001t0011g0016 a0001c0001t0011g0140 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+5944A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615561 | |||||||
chrX:21615736 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2692+6119A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615736 | |||||||
chrX:21616058 | T | C | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+6441T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21616058 | |||||||
chrX:21616359 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2692+6742G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21616359 | |||||||
chrX:21616856 | CTTAA | C | 2 | a0001c0001t0002g0006 a0001c0001t0008g0005 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2692+7243_2692+724 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616856 | ||||||
chrX:21617382 | C | T | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+7765C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617382 | |||||||
chrX:21617695 | T | G | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+8078T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617695 | |||||||
chrX:21617757 | G | A | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+8140G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617757 | |||||||
chrX:21617932 | G | A | 2 | a0001c0001t0022g0032 a0001c0001t0027g0033 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2692+8315G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617932 | |||||||
chrX:21618109 | G | C | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01884.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+8492G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618109 | |||||||
chrX:21618213 | A | T | 3 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0012 |
3 | HG02572.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2692+8596A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618213 | |||||||
chrX:21618364 | A | G | 9 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2692+8747A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618364 | |||||||
chrX:21619057 | A | G | 2 | a0001c0001t0006g0154 a0002c0004t0006g0153 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2692+9440A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619057 | |||||||
chrX:21619690 | C | T | 66 | a0001c0001t0001g0098 a0001c0001t0002g0003 a0001c0001t0002g0006 others(63): Show |
66 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.2692+10073C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619690 | |||||||
chrX:21619837 | T | A | 1 | a0001c0001t0012g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2692+10220T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619837 | |||||||
chrX:21620256 | A | G | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+10639A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21620256 | |||||||
chrX:21620871 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2692+11254C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21620871 | |||||||
chrX:21621018 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2692+11401C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621018 | |||||||
chrX:21621289 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2692+11672T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621289 | |||||||
chrX:21621493 | C | T | 17 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(14): Show |
17 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2692+11876C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621493 | |||||||
chrX:21621508 | G | A | 6 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(3): Show |
6 | HG02615.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+11891G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621508 | |||||||
chrX:21622392 | T | C | 30 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(27): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2692+12775T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21622392 | |||||||
chrX:21623292 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2692+13675T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21623292 | |||||||
chrX:21623542 | T | C | 10 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(7): Show |
10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+13925T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21623542 | |||||||
chrX:21624482 | A | T | 1 | a0001c0001t0027g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2692+14865A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624482 | |||||||
chrX:21624510 | G | T | 1 | a0001c0001t0002g0145 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+14893G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624510 | |||||||
chrX:21624565 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2692+14948G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624565 | |||||||
chrX:21624906 | G | T | 1 | a0001c0001t0002g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2692+15289G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624906 | |||||||
chrX:21625340 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2692+15723G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21625340 | |||||||
chrX:21625678 | C | T | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2692+16061C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21625678 | |||||||
chrX:21626153 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2692+16536T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626153 | |||||||
chrX:21626172 | G | A | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2692+16555G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626172 | |||||||
chrX:21626244 | T | TA | 19 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0002g0006 others(16): Show |
19 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2692+16650dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | ||||||
chrX:21626244 | T | TAA | 7 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0008g0151 others(4): Show |
7 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2692+16649_2692+16 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | ||||||
chrX:21626244 | TA | T | 19 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0003g0043 others(16): Show |
19 | HG00738.hp1 HG01884.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.2692+16650delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | ||||||
chrX:21626268 | T | A | 1 | a0001c0001t0003g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2692+16651T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626268 | |||||||
chrX:21626735 | A | G | 9 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(6): Show |
9 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+17118A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626735 | |||||||
chrX:21626958 | G | C | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2692+17341G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626958 | |||||||
chrX:21627220 | C | T | 11 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0003g0024 others(8): Show |
11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2692+17603C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627220 | |||||||
chrX:21627221 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0157 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2692+17604G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627221 | |||||||
chrX:21627250 | T | G | 2 | a0001c0001t0001g0084 a0001c0001t0028g0002 |
2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2692+17633T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627250 | |||||||
chrX:21627336 | C | CA | 10 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(7): Show |
10 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+17732dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21627336 | ||||||
chrX:21627424 | G | A | 1 | a0001c0001t0024g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+17807G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627424 | |||||||
chrX:21627454 | G | A | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2692+17837G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627454 | |||||||
chrX:21628395 | C | G | 2 | a0001c0001t0007g0020 a0001c0001t0025g0130 |
2 | HG02132.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2692+18778C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628395 | |||||||
chrX:21628726 | C | T | 3 | a0001c0001t0002g0112 a0001c0001t0005g0019 a0001c0001t0005g0021 |
3 | HG00741.hp2 HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2692+19109C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628726 | |||||||
chrX:21628854 | T | A | 1 | a0001c0001t0034g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2692+19237T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628854 | |||||||
chrX:21629422 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-19409C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629422 | |||||||
chrX:21629677 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0004g0088 a0001c0001t0004g0091 others(2): Show |
5 | HG02055.hp1 NA18945.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-19154C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629677 | |||||||
chrX:21629772 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2693-19059G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629772 | |||||||
chrX:21629815 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2693-19016T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629815 | |||||||
chrX:21629859 | G | A | 4 | a0001c0001t0020g0142 a0001c0001t0035g0007 a0001c0003t0014g0148 others(1): Show |
4 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-18972G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629859 | |||||||
chrX:21629881 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-18950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629881 | |||||||
chrX:21630182 | T | G | 3 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-18649T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630182 | |||||||
chrX:21630306 | A | G | 8 | a0001c0001t0002g0026 a0001c0001t0003g0014 a0001c0001t0003g0024 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-18525A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630306 | |||||||
chrX:21630469 | TACA | T | 2 | a0001c0001t0003g0082 a0001c0001t0030g0054 |
2 | NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2693-18356_2693-18 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630469 | ||||||
chrX:21630581 | T | TCAGA | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-18243_2693-18 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630581 | ||||||
chrX:21630698 | T | TAC | 10 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(7): Show |
10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-18121_2693-18 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630698 | ||||||
chrX:21630714 | C | CATAT | 4 | a0001c0001t0001g0098 a0001c0001t0002g0111 a0001c0001t0005g0055 others(1): Show |
4 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-18106_2693-18 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630714 | ||||||
chrX:21630840 | A | C | 10 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(7): Show |
10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-17991A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630840 | |||||||
chrX:21630872 | A | G | 6 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(3): Show |
6 | HG01071.hp2 HG01884.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-17959A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630872 | |||||||
chrX:21631030 | T | A | 7 | a0001c0001t0001g0139 a0001c0001t0007g0141 a0001c0001t0010g0160 others(4): Show |
7 | HG01071.hp2 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2693-17801T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631030 | |||||||
chrX:21631314 | G | A | 5 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-17517G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631314 | |||||||
chrX:21631431 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2693-17400G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631431 | |||||||
chrX:21631450 | G | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-17381G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631450 | |||||||
chrX:21631670 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2693-17161T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631670 | |||||||
chrX:21631848 | A | G | 1 | a0001c0001t0006g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2693-16983A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631848 | |||||||
chrX:21631874 | A | G | 3 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-16957A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631874 | |||||||
chrX:21632392 | T | A | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-16439T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21632392 | |||||||
chrX:21632990 | T | TAC | 16 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 others(13): Show |
16 | HG01071.hp2 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2693-15807_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | ||||||
chrX:21632990 | T | TACAC | 2 | a0001c0003t0014g0148 a0001c0003t0014g0149 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-15809_2693-15 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | ||||||
chrX:21632990 | TAC | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0063 others(5): Show |
8 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-15807_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | ||||||
chrX:21632990 | TACAC | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0109 a0001c0001t0010g0160 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-15809_2693-15 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | ||||||
chrX:21632990 | TACACAC | T | 17 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(14): Show |
17 | HG00621.hp1 HG02074.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.2693-15811_2693-15 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | ||||||
chrX:21633350 | A | G | 3 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 |
3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2693-15481A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633350 | |||||||
chrX:21633417 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0002g0111 a0001c0001t0013g0061 |
3 | HG00735.hp2 HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2693-15414T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633417 | |||||||
chrX:21633580 | A | ACT | 10 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(7): Show |
10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-15249_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21633580 | ||||||
chrX:21633631 | G | A | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-15200G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633631 | |||||||
chrX:21633758 | T | C | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-15073T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633758 | |||||||
chrX:21634066 | A | G | 1 | a0001c0001t0021g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2693-14765A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634066 | |||||||
chrX:21634111 | CT | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2693-14719delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634111 | |||||||
chrX:21634227 | C | G | 7 | a0001c0001t0006g0154 a0001c0001t0006g0159 a0001c0001t0006g0161 others(4): Show |
7 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2693-14604C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634227 | |||||||
chrX:21634491 | G | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-14340G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634491 | |||||||
chrX:21634520 | T | A | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-14311T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634520 | |||||||
chrX:21634879 | C | T | 6 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-13952C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634879 | |||||||
chrX:21635028 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2693-13803C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635028 | |||||||
chrX:21635378 | A | ATG | 2 | a0001c0001t0001g0001 a0001c0001t0032g0085 |
2 | HG04204.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2693-13423_2693-13 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | ||||||
chrX:21635378 | ATG | A | 58 | a0001c0001t0001g0098 a0001c0001t0002g0003 a0001c0001t0002g0006 others(55): Show |
58 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.2693-13423_2693-13 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | ||||||
chrX:21635378 | ATGTG | A | 8 | a0001c0001t0002g0026 a0001c0001t0005g0087 a0001c0001t0007g0141 others(5): Show |
8 | HG00738.hp1 HG01071.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-13425_2693-13 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | ||||||
chrX:21635406 | G | GTATATAT others(23): Show |
1 | a0001c0001t0002g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2693-13424_2693-13 others(36): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635406 | ||||||
chrX:21635408 | G | A | 8 | a0001c0001t0002g0122 a0001c0001t0007g0141 a0001c0001t0010g0160 others(5): Show |
8 | HG01071.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-13423G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635408 | |||||||
chrX:21635410 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2693-13421A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635410 | |||||||
chrX:21635420 | A | C | 4 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 others(1): Show |
4 | HG01071.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-13411A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635420 | |||||||
chrX:21635502 | G | A | 28 | a0001c0001t0003g0028 a0001c0001t0006g0154 a0001c0001t0006g0156 others(25): Show |
28 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-13329G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635502 | |||||||
chrX:21635503 | T | A | 28 | a0001c0001t0003g0028 a0001c0001t0006g0154 a0001c0001t0006g0156 others(25): Show |
28 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-13328T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635503 | |||||||
chrX:21635523 | T | C | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2693-13308T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635523 | |||||||
chrX:21635550 | GTGTATAT others(1): Show |
G | 5 | a0001c0001t0020g0142 a0001c0001t0022g0032 a0001c0001t0027g0033 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-13263_2693-13 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635550 | ||||||
chrX:21635902 | C | T | 1 | a0001c0001t0013g0061 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2693-12929C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635902 | |||||||
chrX:21636277 | G | GA | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-12550dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21636277 | ||||||
chrX:21636305 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2693-12526C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636305 | |||||||
chrX:21636492 | G | C | 1 | a0001c0001t0021g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2693-12339G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636492 | |||||||
chrX:21636902 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2693-11929C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636902 | |||||||
chrX:21636912 | A | C | 1 | a0001c0001t0036g0136 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2693-11919A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636912 | |||||||
chrX:21637154 | C | G | 3 | a0001c0001t0010g0160 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2693-11677C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637154 | |||||||
chrX:21637212 | G | C | 72 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0002g0003 others(69): Show |
72 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2693-11619G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637212 | |||||||
chrX:21637841 | G | T | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2693-10990G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637841 | |||||||
chrX:21638335 | A | C | 3 | a0001c0001t0020g0142 a0001c0003t0014g0148 a0001c0003t0014g0149 |
3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-10496A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638335 | |||||||
chrX:21638368 | T | A | 1 | a0001c0001t0002g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2693-10463T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638368 | |||||||
chrX:21638896 | C | A | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2693-9935C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638896 | |||||||
chrX:21639152 | A | G | 1 | a0001c0001t0006g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2693-9679A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639152 | |||||||
chrX:21639259 | T | C | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-9572T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639259 | |||||||
chrX:21639374 | C | T | 1 | a0001c0001t0019g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2693-9457C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639374 | |||||||
chrX:21639969 | G | A | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2693-8862G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639969 | |||||||
chrX:21639976 | A | G | 4 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-8855A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639976 | |||||||
chrX:21640638 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2693-8193A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21640638 | |||||||
chrX:21640652 | T | C | 5 | a0001c0001t0007g0141 a0001c0001t0010g0160 a0001c0001t0010g0162 others(2): Show |
5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-8179T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21640652 | |||||||
chrX:21642148 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2693-6683A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642148 | |||||||
chrX:21642170 | C | A | 5 | a0001c0001t0006g0154 a0001c0001t0006g0159 a0001c0001t0006g0161 others(2): Show |
5 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2693-6661C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642170 | |||||||
chrX:21642182 | C | T | 28 | a0001c0001t0002g0018 a0001c0001t0006g0154 a0001c0001t0006g0156 others(25): Show |
28 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-6649C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642182 | |||||||
chrX:21643079 | T | C | 1 | a0001c0001t0020g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-5752T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643079 | |||||||
chrX:21643532 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-5299A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643532 | |||||||
chrX:21643684 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2693-5147T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643684 | |||||||
chrX:21644379 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2693-4452A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644379 | |||||||
chrX:21644665 | T | A | 1 | a0001c0003t0026g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2693-4166T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644665 | |||||||
chrX:21644850 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0016g0070 |
2 | HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2693-3981T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644850 | |||||||
chrX:21645851 | T | C | 4 | a0001c0001t0011g0015 a0001c0001t0011g0016 a0001c0001t0011g0140 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-2980T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21645851 | |||||||
chrX:21645863 | C | A | 1 | a0001c0001t0012g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2693-2968C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21645863 | |||||||
chrX:21646274 | A | G | 2 | a0001c0001t0012g0044 a0001c0001t0012g0143 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2693-2557A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21646274 | |||||||
chrX:21646932 | G | C | 15 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(12): Show |
15 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2693-1899G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21646932 | |||||||
chrX:21647077 | C | T | 1 | a0001c0007t0031g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-1754C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647077 | |||||||
chrX:21647148 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2693-1683T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647148 | |||||||
chrX:21647150 | T | G | 13 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2693-1681T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647150 | |||||||
chrX:21647921 | T | C | 1 | a0001c0001t0006g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2693-910T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647921 | |||||||
chrX:21647922 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2693-909C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647922 | |||||||
chrX:21648069 | A | G | 1 | a0001c0002t0001g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2693-762A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648069 | |||||||
chrX:21648386 | A | G | 4 | a0001c0001t0002g0006 a0001c0001t0003g0030 a0001c0001t0008g0005 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-445A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648386 | |||||||
chrX:21648395 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-436C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648395 | |||||||
chrX:21648616 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2693-215A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648616 | |||||||
chrX:21648788 | C | T | 1 | a0001c0002t0007g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2693-43C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648788 | |||||||
chrX:21648792 | T | C | 2 | a0001c0001t0011g0016 a0001c0001t0012g0025 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2693-39T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648792 | |||||||
chrX:21648794 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(95): Show |
98 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.2693-12dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | ||||||
chrX:21648794 | C | CTT | 12 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0157 others(9): Show |
12 | HG00642.hp1 HG01192.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2693-13_2693-12dup others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | ||||||
chrX:21648794 | C | CTTT | 7 | a0001c0001t0009g0009 a0001c0001t0011g0015 a0001c0001t0011g0140 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2693-14_2693-12dup others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | ||||||
chrX:21648794 | C | T | 1 | a0001c0001t0035g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-37C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648794 | |||||||
chrX:21649865 | C | T | 7 | a0001c0001t0002g0045 a0001c0001t0002g0119 a0001c0001t0002g0120 others(4): Show |
7 | HG02083.hp1 NA18612.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+838C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21649865 | |||||||
chrX:21650278 | G | A | 31 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(28): Show |
31 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2889+1251G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650278 | |||||||
chrX:21650280 | A | G | 1 | a0001c0001t0021g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2889+1253A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650280 | |||||||
chrX:21650340 | C | T | 1 | a0001c0001t0007g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2889+1313C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650340 | |||||||
chrX:21650425 | G | A | 1 | a0001c0001t0006g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2889+1398G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650425 | |||||||
chrX:21650695 | T | G | 15 | a0001c0001t0006g0154 a0001c0001t0006g0156 a0001c0001t0006g0158 others(12): Show |
15 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2890-1611T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650695 | |||||||
chrX:21650724 | G | C | 1 | a0001c0001t0002g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2890-1582G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650724 | |||||||
chrX:21651166 | T | C | 1 | a0001c0001t0009g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2890-1140T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21651166 | |||||||
chrX:21651461 | C | A | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2890-845C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21651461 | |||||||
chrX:21652095 | G | C | 1 | a0001c0003t0026g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2890-211G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21652095 | |||||||
chrX:21652272 | C | T | 1 | a0001c0001t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2890-34C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21652272 |