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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
32201182
G
A
intron_variant
MODIFIER
GPD1L
c.959+16G>A
chr3
32200233
G
A
intron_variant
MODIFIER
GPD1L
c.619-135G>A
chr3
32187990
C
G
intron_variant
MODIFIER
GPD1L
c.506-124C>G
chr3
32181684
G
A
intron_variant
MODIFIER
GPD1L
c.367-36G>A
chr3
24009279
A
C
intron_variant
MODIFIER
NR1D2
c.1333-25A>C
chr3
24006477
T
A
missense_variant
MODERATE
NR1D2
c.1156T>A
chr3
24001078
C
T
intron_variant
MODIFIER
NR1D2
c.373-84C>T
chr3
12650847
T
TA
intron_variant
MODIFIER
RAF1
c.321-14_321-13insT
chr3
12650482
T
A
intron_variant
MODIFIER
RAF1
c.424-60A>T
chr3
10142949
C
T
3_prime_UTR_variant
MODIFIER
FANCD2
c.*3C>T
chr3
10128965
CT
C
intron_variant
MODIFIER
FANCD2
c.3466+18delT
chr3
10105665
C
G
intron_variant
MODIFIER
FANCD2
c.1947+70C>G
chr3
10105661
CT
C
intron_variant
MODIFIER
FANCD2
c.1947+67delT
chr3
10091252
A
C
intron_variant
MODIFIER
FANCD2
c.1545+63A>C
chr3
10091035
T
C
intron_variant
MODIFIER
FANCD2
c.1414-23T>C
chr3
10089886
G
T
intron_variant
MODIFIER
FANCD2
c.1413+151G>T
chr3
10089852
A
G
intron_variant
MODIFIER
FANCD2
c.1413+117A>G
chr3
10089841
C
A
intron_variant
MODIFIER
FANCD2
c.1413+106C>A
chr3
10089834
A
T
intron_variant
MODIFIER
FANCD2
c.1413+99A>T
chr3
10089828
G
A
intron_variant
MODIFIER
FANCD2
c.1413+93G>A