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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
119013928
A
T
intron_variant
MODIFIER
ARHGAP31
c.100+77A>T
chr3
111356083
G
C
synonymous_variant
LOW
CD96
c.1410G>C
chr3
111343069
C
T
intron_variant
MODIFIER
CD96
c.1298-111C>T
chr3
111316886
C
CTTATG
intron_variant
MODIFIER
CD96
c.856-81_856-80insTTATG
chr3
111286375
G
C
missense_variant
MODERATE
CD96
c.424G>C
chr3
69059023
A
C
intron_variant
MODIFIER
EOGT
c.-14-12T>G
chr3
69053447
A
T
intron_variant
MODIFIER
EOGT
c.620+82T>A
chr3
69038217
A
G
intron_variant
MODIFIER
EOGT
c.832-49T>C
chr3
69037633
G
C
intron_variant
MODIFIER
EOGT
c.996+24C>G
chr3
69036707
G
A
intron_variant
MODIFIER
EOGT
c.1084-43C>T
chr3
69025792
C
CGTGTGTGTGT
3_prime_UTR_variant
MODIFIER
EOGT
c.*967_*976dupACACACACAC
chr3
58156242
C
T
intron_variant
MODIFIER
FLNB
c.7715-60C>T
chr3
58156176
G
A
intron_variant
MODIFIER
FLNB
c.7715-126G>A
chr3
58154327
C
T
synonymous_variant
LOW
FLNB
c.7452C>T
chr3
58145263
G
A
intron_variant
MODIFIER
FLNB
c.6982-18G>A
chr3
58121626
T
A
intron_variant
MODIFIER
FLNB
c.4765-80T>A
chr3
58118700
A
G
intron_variant
MODIFIER
FLNB
c.4607+42A>G
chr3
58118555
G
A
missense_variant
MODERATE
FLNB
c.4504G>A
chr3
58116369
T
C
intron_variant
MODIFIER
FLNB
c.4223-99T>C
chr3
58116358
C
T
intron_variant
MODIFIER
FLNB
c.4223-110C>T