List of variants studied for Fanconi anemia, complementation group D1 by OMIM

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Total variants: 15

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HGVS	dbSNP
NM_000059.3(BRCA2):c.4648G>T (p.Glu1550Ter)	rs80358695
NM_000059.3(BRCA2):c.5609_5610delinsAG (p.Phe1870Ter)	rs276174859
NM_000059.3(BRCA2):c.5946del (p.Ser1982fs)	rs80359550
NM_000059.3(BRCA2):c.631+1G>A	rs81002897
NM_000059.3(BRCA2):c.631+2T>G	rs81002899
NM_000059.3(BRCA2):c.658_659del (p.Val220fs)	rs80359604
NM_000059.3(BRCA2):c.7007G>A (p.Arg2336His)	rs28897743
NM_000059.3(BRCA2):c.7464_7465insTA (p.Asp2489Ter)	rs886038169
NM_000059.3(BRCA2):c.7529T>C (p.Leu2510Pro)	rs80358979
NM_000059.3(BRCA2):c.8187G>T (p.Lys2729Asn)	rs80359065
NM_000059.3(BRCA2):c.8219T>A (p.Leu2740Ter)	rs80359070
NM_000059.3(BRCA2):c.8488-1G>A	rs397507404
NM_000059.3(BRCA2):c.8732C>A (p.Ala2911Glu)	rs80359130
NM_000059.3(BRCA2):c.9196C>T (p.Gln3066Ter)	rs80359180
NM_000059.3(BRCA2):c.9672dup (p.Tyr3225fs)	rs80359773

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