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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr9
94518328
C
T
intron_variant
MODIFIER
ROR2
c.494+25G>A
chr9
94499618
G
A
intron_variant
MODIFIER
ROR2
c.622+55C>T
chr9
94495608
T
C
missense_variant
MODERATE
ROR2
c.733A>G
chr9
94487459
C
T
intron_variant
MODIFIER
ROR2
c.1387-70G>A
chr9
94486688
G
A
synonymous_variant
LOW
ROR2
c.2088C>T
chr9
94486321
C
T
missense_variant
MODERATE
ROR2
c.2455G>A
chr9
94485928
C
T
3_prime_UTR_variant
MODIFIER
ROR2
c.*16G>A
chr8
145699601
T
C
3_prime_UTR_variant
MODIFIER
FOXH1
c.*20A>G
chr8
106815894
A
AGACTT
3_prime_UTR_variant
MODIFIER
ZFPM2
c.*129_*133dupGACTT
chr8
106646683
A
T
intron_variant
MODIFIER
ZFPM2
c.532+98A>T
chr8
106573578
C
T
intron_variant
MODIFIER
ZFPM2
c.302-13C>T
chr8
106573524
CA
C
intron_variant
MODIFIER
ZFPM2
c.302-66delA
chr8
106456683
A
G
intron_variant
MODIFIER
ZFPM2
c.301+74A>G
chr8
106431589
T
TA
intron_variant
MODIFIER
ZFPM2
c.199+59_199+60insA
chr8
100844758
T
C
synonymous_variant
LOW
VPS13B
c.9567T>C
chr8
100479917
T
C
intron_variant
MODIFIER
VPS13B
c.3666+55T>C
chr8
100287517
CTT
CT
intron_variant
MODIFIER
VPS13B
c.2824+37delT
chr8
100287517
CTT
C
intron_variant
MODIFIER
VPS13B
c.2824+36_2824+37delTT
chr8
100160282
ATT
A
intron_variant
MODIFIER
VPS13B
c.2013+45_2013+46delTT
chr8
100133706
T
G
stop_gained
HIGH
VPS13B
c.1239T>G