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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
24006477
T
A
missense_variant
MODERATE
NR1D2
c.1156T>A
chr3
12650482
T
A
intron_variant
MODIFIER
RAF1
c.424-60A>T
chr3
12645007
C
T
intron_variant
MODIFIER
RAF1
c.834+628G>A
chr3
10140696
A
G
3_prime_UTR_variant
MODIFIER
FANCD2
c.*62A>G
chr3
10140671
G
A
3_prime_UTR_variant
MODIFIER
FANCD2
c.*37G>A
chr3
10138069
T
G
synonymous_variant
LOW
FANCD2
c.4098T>G
chr3
10136150
C
T
intron_variant
MODIFIER
FANCD2
c.3963+103C>T
chr3
10133949
A
G
intron_variant
MODIFIER
FANCD2
c.3849+13A>G
chr3
10132127
ATTTT
A
intron_variant
MODIFIER
FANCD2
c.3777+59_3777+62delTTTT
chr3
10119917
T
C
intron_variant
MODIFIER
FANCD2
c.2976+36T>C
chr3
10114802
T
C
intron_variant
MODIFIER
FANCD2
c.2606-135T>C
chr3
10107520
G
T
intron_variant
MODIFIER
FANCD2
c.2270-28G>T
chr3
10106532
C
T
missense_variant
MODERATE
FANCD2
c.2141C>T
chr3
10106408
C
T
splice_region_variant&intron_variant
LOW
FANCD2
c.2022-5C>T
chr3
10106386
A
G
intron_variant
MODIFIER
FANCD2
c.2022-27A>G
chr3
10106144
C
T
intron_variant
MODIFIER
FANCD2
c.2021+31C>T
chr3
10105661
CT
C
intron_variant
MODIFIER
FANCD2
c.1947+67delT
chr3
10094206
AT
A
intron_variant
MODIFIER
FANCD2
c.1656+26delT
chr3
10089886
G
T
intron_variant
MODIFIER
FANCD2
c.1413+151G>T
chr3
10089852
A
G
intron_variant
MODIFIER
FANCD2
c.1413+117A>G