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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr19
39008003
G
A
synonymous_variant
LOW
RYR1
c.9690G>A
chr19
39002725
A
G
synonymous_variant
LOW
RYR1
c.9186A>G
chr19
39000946
A
G
intron_variant
MODIFIER
RYR1
c.8933-192A>G
chr19
38998497
G
GC
intron_variant
MODIFIER
RYR1
c.8932+30_8932+31insC
chr19
38997679
G
T
intron_variant
MODIFIER
RYR1
c.8816+87G>T
chr19
38997635
A
C
intron_variant
MODIFIER
RYR1
c.8816+43A>C
chr19
38997609
T
A
intron_variant
MODIFIER
RYR1
c.8816+17T>A
chr19
38997459
G
C
intron_variant
MODIFIER
RYR1
c.8693-10G>C
chr19
38997364
T
TTCA
intron_variant
MODIFIER
RYR1
c.8693-105_8693-104insTCA
chr19
38997214
T
G
intron_variant
MODIFIER
RYR1
c.8692+28T>G
chr19
38997076
C
T
intron_variant
MODIFIER
RYR1
c.8617-35C>T
chr19
38996990
T
C
synonymous_variant
LOW
RYR1
c.8589T>C
chr19
38996623
T
G
intron_variant
MODIFIER
RYR1
c.8541+37T>G
chr19
38996620
C
T
intron_variant
MODIFIER
RYR1
c.8541+34C>T
chr19
38996066
A
G
intron_variant
MODIFIER
RYR1
c.8400+28A>G
chr19
38995975
G
A
synonymous_variant
LOW
RYR1
c.8337G>A
chr19
38995510
T
C
synonymous_variant
LOW
RYR1
c.8190T>C
chr19
38995438
T
C
synonymous_variant
LOW
RYR1
c.8118T>C
chr19
38995355
ACCT
A
intron_variant
MODIFIER
RYR1
c.8068-32_8068-30delCCT
chr19
38994910
G
A
synonymous_variant
LOW
RYR1
c.7977G>A