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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr10
123549544
T
TACAC
intron_variant
MODIFIER
ATE1
c.1378+139_1378+140insGTGT
chr10
123298158
T
C
synonymous_variant
LOW
FGFR2
c.696A>G
chr10
123286375
T
C
intron_variant
MODIFIER
FGFR2
c.749-6692A>G
chr10
123279745
C
T
intron_variant
MODIFIER
FGFR2
c.749-62G>A
chr10
123263616
C
T
intron_variant
MODIFIER
FGFR2
c.1291-161G>A
chr10
123241794
C
T
intron_variant
MODIFIER
FGFR2
c.2304+1418G>A
chr10
112764594
T
C
intron_variant
MODIFIER
SHOC2
c.1161+42T>C
chr10
97447487
T
A
intron_variant
MODIFIER
TCTN3
c.500-11A>T
chr10
97447373
A
T
synonymous_variant
LOW
TCTN3
c.603T>A
chr10
97446206
G
A
intron_variant
MODIFIER
TCTN3
c.888+46C>T
chr10
97445501
CCT
C
intron_variant
MODIFIER
TCTN3
c.889-110_889-109delAG
chr10
97440107
CA
C
intron_variant
MODIFIER
TCTN3
c.1590+121delT
chr10
97440106
A
G
intron_variant
MODIFIER
TCTN3
c.1590+123T>C
chr10
97440103
T
TGG
intron_variant
MODIFIER
TCTN3
c.1590+125_1590+126insCC
chr10
97440098
CACT
C
intron_variant
MODIFIER
TCTN3
c.1590+128_1590+130delAGT
chr10
92680929
A
G
5_prime_UTR_variant
MODIFIER
ANKRD1
c.-145T>C
chr10
92678765
A
G
intron_variant
MODIFIER
ANKRD1
c.346-36T>C
chr10
92678740
AATAAATAAATATATATAT
A
intron_variant
MODIFIER
ANKRD1
c.346-29_346-12delATATATATATTTATTTAT
chr10
92676127
T
C
intron_variant
MODIFIER
ANKRD1
c.553-101A>G
chr10
92672564
T
C
3_prime_UTR_variant
MODIFIER
ANKRD1
c.*59A>G