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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
58112556
G
C
intron_variant
MODIFIER
FLNB
c.4222+67G>C
chr3
58112488
C
T
splice_region_variant&synonymous_variant
LOW
FLNB
c.4221C>T
chr3
58112440
A
G
synonymous_variant
LOW
FLNB
c.4173A>G
chr3
58112251
A
G
intron_variant
MODIFIER
FLNB
c.4062-78A>G
chr3
58111285
T
G
intron_variant
MODIFIER
FLNB
c.3899-23T>G
chr3
58109162
G
A
missense_variant
MODERATE
FLNB
c.3469G>A
chr3
58095500
G
T
intron_variant
MODIFIER
FLNB
c.2323+74G>T
chr3
58095466
G
T
intron_variant
MODIFIER
FLNB
c.2323+40G>T
chr3
58094852
C
T
intron_variant
MODIFIER
FLNB
c.2056-54C>T
chr3
58094157
A
G
intron_variant
MODIFIER
FLNB
c.1942-28A>G
chr3
58089877
A
G
intron_variant
MODIFIER
FLNB
c.1610+65A>G
chr3
58089585
T
A
intron_variant
MODIFIER
FLNB
c.1484-101T>A
chr3
58083446
G
A
intron_variant
MODIFIER
FLNB
c.985-96G>A
chr3
58081888
T
C
synonymous_variant
LOW
FLNB
c.927T>C
chr3
58080505
G
T
intron_variant
MODIFIER
FLNB
c.788-58G>T
chr3
57994677
C
T
intron_variant
MODIFIER
FLNB
c.292+94C>T
chr3
55520778
T
G
intron_variant
MODIFIER
WNT5A
c.6+230A>C
chr3
53779580
G
C
intron_variant
MODIFIER
CACNA1D
c.3067-71G>C
chr3
53778621
G
A
intron_variant
MODIFIER
CACNA1D
c.2979-146G>A
chr3
53776995
T
C
intron_variant
MODIFIER
CACNA1D
c.2872-43T>C