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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr19
55668509
A
T
intron_variant
MODIFIER
TNNI3
c.23-9T>A
chr19
55668310
C
G
intron_variant
MODIFIER
TNNI3
c.105+108G>C
chr19
55668197
T
G
intron_variant
MODIFIER
TNNI3
c.106-185A>C
chr19
55668144
T
C
intron_variant
MODIFIER
TNNI3
c.106-132A>G
chr19
55667958
C
T
intron_variant
MODIFIER
TNNI3
c.147+13G>A
chr19
55667500
A
T
intron_variant
MODIFIER
TNNI3
c.279+69T>A
chr19
55665689
C
G
intron_variant
MODIFIER
TNNI3
c.370-115G>C
chr19
55665584
A
C
intron_variant
MODIFIER
TNNI3
c.370-10T>G
chr19
49686055
C
G
missense_variant
MODERATE
TRPM4
c.1484C>G
chr19
49685708
CCCAT
C
intron_variant
MODIFIER
TRPM4
c.1264-126_1264-123delCCAT
chr19
49684787
CTT
C
intron_variant
MODIFIER
TRPM4
c.1263+70_1263+71delTT
chr19
42883065
AAAGGGGG
A
downstream_gene_variant
MODIFIER
MEGF8
c.*9173_*9173delAAGGGGG
chr19
42882829
TA
T
3_prime_UTR_variant
MODIFIER
MEGF8
c.*1903delA
chr19
42879964
C
T
synonymous_variant
LOW
MEGF8
c.7575C>T
chr19
42848764
A
G
intron_variant
MODIFIER
MEGF8
c.1933+27A>G
chr19
42375244
C
T
intron_variant
MODIFIER
RPS19
c.412-175C>T
chr19
42373893
C
T
intron_variant
MODIFIER
RPS19
c.411+70C>T
chr19
42373679
C
T
intron_variant
MODIFIER
RPS19
c.357-90C>T
chr19
42373298
G
A
intron_variant
MODIFIER
RPS19
c.356+14G>A
chr19
42367914
C
CTT
intron_variant
MODIFIER
RPS19
c.172+2633_172+2634insTT