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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr10
126677961
C
A
3_prime_UTR_variant
MODIFIER
CTBP2
c.*126G>T
chr10
126677950
C
T
3_prime_UTR_variant
MODIFIER
CTBP2
c.*137G>A
chr10
126677944
T
C
3_prime_UTR_variant
MODIFIER
CTBP2
c.*143A>G
chr10
126677938
C
G
3_prime_UTR_variant
MODIFIER
CTBP2
c.*149G>C
chr10
123683935
T
G
intron_variant
MODIFIER
ATE1
c.107-91A>C
chr10
123673339
T
C
synonymous_variant
LOW
ATE1
c.303A>G
chr10
123600590
A
G
splice_region_variant&intron_variant
LOW
ATE1
c.1157+7T>C
chr10
123596254
T
C
synonymous_variant
LOW
ATE1
c.1236A>G
chr10
123503431
CTT
C
intron_variant
MODIFIER
ATE1
c.1379-60_1379-59delAA
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
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