view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | 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 | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM86B2_chr8_12419421_12441400 | 12422041 | T | TTTATTAT others(11): Show |
downstream_gene_variant | MODIFIER | HG02976.hp1 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0002 | 1 | 50 | 0.0200 | 18 | c.*38 others(29): Show |
FAM86B2 | ENSG00000145002.13 | transcript | ENST00000262365.9 | protein_coding | 2379 | chr8 | TogoVar | |||||||
FAM89A_chr1_231013958_231045254 | 231024520 | G | GCACACAC others(11): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(1): Show | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0043 others(23): Show |
32 | 450 | 0.0711 | 18 | c.292 others(35): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 1/1 | chr1 | TogoVar | |||||||
FAM89A_chr1_231013958_231045254 | 231043452 | G | GGAGCGCC others(11): Show |
upstream_gene_variant | MODIFIER | NA19012.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0328 | 1 | 450 | 0.0022 | 18 | c.-32 others(29): Show |
FAM89A | ENSG00000182118.8 | transcript | ENST00000366654.5 | protein_coding | 3199 | chr1 | TogoVar | |||||||
FAM98B_chr15_38449127_38492710 | 38462126 | A | AAATGTAT others(11): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00609.hp2 HG01168.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0025 others(8): Show |
22 | 400 | 0.0550 | 18 | c.72- others(33): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
FAM98B_chr15_38449127_38492710 | 38469211 | C | CCTACCGT others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0014a0003c0005others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
140 | 400 | 0.3500 | 18 | c.353 others(35): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022399 | A | ATATTATA others(11): Show |
downstream_gene_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 258 | 0.0039 | 18 | c.*30 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1832 | chrX | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022427 | A | ATATTATA others(11): Show |
downstream_gene_variant | MODIFIER | HG00544.hp1 NA19076.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0019 |
2 | 258 | 0.0078 | 18 | c.*29 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1804 | chrX | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022677 | T | TTATGTAT others(11): Show |
downstream_gene_variant | MODIFIER | NA18950.hp2 NA18977.hp1 NA18988.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0006g0036 |
3 | 258 | 0.0116 | 18 | c.*27 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1554 | chrX | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022751 | T | TTATGTAT others(11): Show |
downstream_gene_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG01346.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
3 | 258 | 0.0116 | 18 | c.*26 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1480 | chrX | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022779 | T | TTATGTAT others(11): Show |
downstream_gene_variant | MODIFIER | HG01081.hp1 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 a0001c0001t0001g0027 |
2 | 258 | 0.0078 | 18 | c.*26 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1452 | chrX | TogoVar | |||||||
FAM9B_chrX_9019232_9039127 | 9022807 | T | TTATGTAT others(11): Show |
downstream_gene_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 258 | 0.0039 | 18 | c.*26 others(29): Show |
FAM9B | ENSG00000177138.17 | transcript | ENST00000327220.10 | protein_coding | 1424 | chrX | TogoVar | |||||||
FANCA_chr16_89732549_89821647 | 89759318 | T | TTAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
a0003a0032 | a0003c0003a0032c0043 | a0003c0003t0002a0032c0043t0015 | a0003c0003t0002g0242 a0003c0003t0002g0257 a0003c0003t0002g0268 others(1): Show |
4 | 334 | 0.0120 | 18 | c.285 others(35): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 29/42 | chr16 | TogoVar | |||||||
FANCA_chr16_89732549_89821647 | 89774729 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0036 | a0036c0021 | a0036c0021t0002 | a0036c0021t0002g0012 | 1 | 334 | 0.0030 | 18 | c.190 others(36): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 21/42 | chr16 | TogoVar | |||||||
FANCA_chr16_89732549_89821647 | 89812646 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(2): Show |
a0009a0014 | a0009c0010a0014c0015 | a0009c0010t0002a0014c0015t0002 | a0009c0010t0002g0287 a0009c0010t0002g0288 a0009c0010t0002g0298 others(2): Show |
5 | 334 | 0.0150 | 18 | c.284 others(35): Show |
FANCA | ENSG00000187741.16 | transcript | ENST00000389301.8 | protein_coding | 3/42 | chr16 | TogoVar | |||||||
FANCC_chr9_95094054_95322709 | 95170637 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01934.hp1 HG02055.hp2 others(2): Show |
a0001a0007 | a0001c0001a0007c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0214 a0001c0001t0001g0227 a0001c0001t0002g0052 others(2): Show |
5 | 278 | 0.0180 | 18 | c.521 others(33): Show |
FANCC | ENSG00000158169.14 | transcript | ENST00000289081.8 | protein_coding | 6/14 | chr9 | TogoVar | |||||||
FANCC_chr9_95094054_95322709 | 95271927 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0138 | 1 | 278 | 0.0036 | 18 | c.-78 others(37): Show |
FANCC | ENSG00000158169.14 | transcript | ENST00000289081.8 | protein_coding | 1/14 | chr9 | TogoVar | |||||||
FANCD2_chr3_10021437_10106932 | 10036086 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0006 | a0002c0002t0002g0188 a0002c0002t0002g0189 a0002c0002t0002g0190 others(4): Show |
7 | 242 | 0.0289 | 18 | c.439 others(33): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
FANCG_chr9_35068839_35084942 | 35072568 | T | TGGCAGCG others(11): Show |
downstream_gene_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 426 | 0.0024 | 18 | c.*15 others(29): Show |
FANCG | ENSG00000221829.11 | transcript | ENST00000378643.8 | protein_coding | 1270 | chr9 | TogoVar | |||||||
FANCI_chr15_89238979_89322131 | 89286977 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG03195.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0088 a0001c0004t0003g0096 a0001c0004t0003g0103 |
3 | 346 | 0.0087 | 18 | c.182 others(37): Show |
FANCI | ENSG00000140525.20 | transcript | ENST00000310775.12 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125906515 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01358.hp1 HG02738.hp1 NA18940.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0237 others(4): Show |
7 | 370 | 0.0189 | 18 | c.13+ others(33): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125914280 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01106.hp2 others(13): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0001 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0153 others(13): Show |
16 | 370 | 0.0432 | 18 | c.13+ others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125918585 | A | AAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0132 | 1 | 370 | 0.0027 | 18 | c.13+ others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125918585 | A | AAAAAATA others(11): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0144 | 1 | 370 | 0.0027 | 18 | c.13+ others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125918585 | A | AAAATATA others(11): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0347 | 1 | 370 | 0.0027 | 18 | c.13+ others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125919195 | A | ATTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01934.hp1 HG02818.hp2 HG02886.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0072 a0001c0001t0002g0132 a0001c0001t0002g0204 |
3 | 370 | 0.0081 | 18 | c.13+ others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FANK1_chr10_125891564_126014592 | 125991250 | G | GGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(17): Show |
a0001a0004 | a0001c0001a0004c0009 | a0001c0001t0001a0001c0001t0002a0004c0009t0001 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0062 others(17): Show |
20 | 370 | 0.0541 | 18 | c.316 others(35): Show |
FANK1 | ENSG00000203780.12 | transcript | ENST00000368693.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FAP_chr2_162165684_162248445 | 162247864 | A | ATCTGGGT others(11): Show |
upstream_gene_variant | MODIFIER | NA18982.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0045 | 1 | 234 | 0.0043 | 18 | c.-45 others(29): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4420 | chr2 | TogoVar | |||||||
FAR1_chr11_13663668_13737346 | 13708447 | G | GCGCACAC others(11): Show |
intron_variant | MODIFIER | HG01168.hp2 HG02717.hp1 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0011 | a0001c0001t0004g0299 a0001c0001t0011g0278 a0001c0001t0011g0280 |
3 | 352 | 0.0085 | 18 | c.545 others(33): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAR2_chr12_29144278_29340616 | 29217984 | A | AGAGGAGG others(11): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0204 | 1 | 326 | 0.0031 | 18 | c.-38 others(37): Show |
FAR2 | ENSG00000064763.12 | transcript | ENST00000536681.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
FAR2_chr12_29144278_29340616 | 29308707 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0002 | a0001c0002t0016 | a0001c0002t0016g0223 | 1 | 326 | 0.0031 | 18 | c.724 others(33): Show |
FAR2 | ENSG00000064763.12 | transcript | ENST00000536681.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98151660 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03098.hp1 HG03239.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0003 | a0001c0001t0007g0002 a0001c0002t0003g0207 |
2 | 218 | 0.0092 | 18 | c.-24 others(35): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98207908 | C | CCACACAC others(11): Show |
intron_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0001 | a0001c0001t0070 | a0001c0001t0070g0075 | 1 | 218 | 0.0046 | 18 | c.-23 others(35): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98259882 | A | AGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG01978.hp2 HG02056.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(6): Show | a0001c0001t0002g0035 a0001c0001t0004g0123 a0001c0001t0005g0082 others(9): Show |
12 | 218 | 0.0551 | 18 | c.171 others(37): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98277109 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01257.hp1 HG01257.hp2 others(19): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | a0001c0001t0002g0101 a0001c0001t0004g0009 a0001c0001t0007g0002 others(19): Show |
22 | 218 | 0.1009 | 18 | c.171 others(37): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98277148 | A | ACACACAC others(11): Show |
intron_variant | MODIFIER | HG02080.hp1 NA19004.hp1 NA19004.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0002t0006a0001c0002t0071 | a0001c0001t0014g0076 a0001c0002t0006g0102 a0001c0002t0071g0094 |
3 | 218 | 0.0138 | 18 | c.171 others(37): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98365894 | G | GGTGTGTG others(11): Show |
intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0108 | 1 | 218 | 0.0046 | 18 | c.319 others(33): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98365913 | G | GTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG03098.hp1 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0045a0001c0002t0003 | a0001c0001t0045g0019 a0001c0002t0003g0207 |
2 | 218 | 0.0092 | 18 | c.319 others(33): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98373533 | G | GACAGACA others(11): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02717.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0001 | a0001c0001t0004g0009 a0001c0002t0001g0049 |
2 | 218 | 0.0092 | 18 | c.399 others(35): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP1_chr13_98138094_98460176 | 98379080 | G | GTAATATA others(11): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02622.hp1 HG02630.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0003a0001c0002t0010 | a0001c0001t0004g0011 a0001c0002t0003g0195 a0001c0002t0010g0212 |
3 | 218 | 0.0138 | 18 | c.496 others(35): Show |
FARP1 | ENSG00000152767.17 | transcript | ENST00000319562.11 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
FARP2_chr2_241351285_241499841 | 241396958 | G | GATTAAGA others(11): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0370 | 1 | 378 | 0.0027 | 18 | c.184 others(35): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FARP2_chr2_241351285_241499841 | 241402845 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 378 | 0.0027 | 18 | c.184 others(33): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FARP2_chr2_241351285_241499841 | 241402880 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG01934.hp1 NA18962.hp2 NA18966.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0090 |
3 | 378 | 0.0079 | 18 | c.184 others(33): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FARP2_chr2_241351285_241499841 | 241402880 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 378 | 0.0027 | 18 | c.184 others(33): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FARP2_chr2_241351285_241499841 | 241497033 | C | CGCTGGGG others(11): Show |
downstream_gene_variant | MODIFIER | HG01496.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0190 | 1 | 378 | 0.0027 | 18 | c.*29 others(29): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2193 | chr2 | TogoVar | |||||||
FARS2_chr6_5256513_5776583 | 5341257 | T | TTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0095 | 1 | 170 | 0.0059 | 18 | c.-21 others(37): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 1/6 | chr6 | TogoVar | |||||||
FARS2_chr6_5256513_5776583 | 5405480 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03834.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0046 a0001c0001t0002g0116 |
2 | 170 | 0.0118 | 18 | c.772 others(33): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FARS2_chr6_5256513_5776583 | 5407043 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0034 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | 170 | 0.0529 | 18 | c.772 others(35): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FARS2_chr6_5256513_5776583 | 5407066 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01517.hp1 HG01952.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0057 others(3): Show |
6 | 170 | 0.0353 | 18 | c.772 others(35): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FARS2_chr6_5256513_5776583 | 5514089 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0108 | 1 | 170 | 0.0059 | 18 | c.905 others(37): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FARS2_chr6_5256513_5776583 | 5532774 | T | TAAGAAGA others(11): Show |
intron_variant | MODIFIER | HG03098.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0112 a0001c0001t0002g0114 |
2 | 170 | 0.0118 | 18 | c.905 others(37): Show |
FARS2 | ENSG00000145982.13 | transcript | ENST00000274680.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |