List of variants in gene FGFR2 studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 34

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HGVS	dbSNP
NM_022970.3(FGFR2):c.*259C>T	rs1047057
NM_022970.3(FGFR2):c.-151+19G>T	rs974988741
NM_022970.3(FGFR2):c.-157A>G	rs41258305
NM_022970.3(FGFR2):c.1087+1221C>T	rs201717227
NM_022970.3(FGFR2):c.1087+1290T>C	rs886038254
NM_022970.3(FGFR2):c.1087+1383T>C	rs1554928776
NM_022970.3(FGFR2):c.1089G>A (p.Ala363=)	rs151250769
NM_022970.3(FGFR2):c.109+10T>G	rs3135722
NM_022970.3(FGFR2):c.1365G>A (p.Thr455=)	rs200183009
NM_022970.3(FGFR2):c.1542C>T (p.Thr514=)	rs74160617
NM_022970.3(FGFR2):c.1575A>G (p.Thr525=)	rs74160613
NM_022970.3(FGFR2):c.159G>A (p.Ala53=)	rs1047102
NM_022970.3(FGFR2):c.1676-12C>T	rs41293763
NM_022970.3(FGFR2):c.170C>T (p.Ser57Leu)	rs56226109
NM_022970.3(FGFR2):c.1791G>A (p.Glu597=)	rs56335660
NM_022970.3(FGFR2):c.17G>C (p.Arg6Pro)	rs3750819
NM_022970.3(FGFR2):c.1867-17T>G	rs3135802
NM_022970.3(FGFR2):c.1944C>T (p.Leu648=)	rs35337478
NM_022970.3(FGFR2):c.1989+7C>T	rs199697707
NM_022970.3(FGFR2):c.2193C>T (p.Asn731=)	rs55637244
NM_022970.3(FGFR2):c.2286C>T (p.Leu762=)	rs753103160
NM_022970.3(FGFR2):c.2304+1526A>G	rs189179463
NM_022970.3(FGFR2):c.2304+15C>T	rs2278202
NM_022970.3(FGFR2):c.2332G>A (p.Glu778Lys)	rs374993905
NM_022970.3(FGFR2):c.23T>G (p.Ile8Ser)	rs147307031
NM_022970.3(FGFR2):c.294G>A (p.Thr98=)	rs1047101
NM_022970.3(FGFR2):c.309C>A (p.Gly103=)	rs749255726
NM_022970.3(FGFR2):c.34G>A (p.Val12Met)	rs143978938
NM_022970.3(FGFR2):c.420G>A (p.Ala140=)	rs765024365
NM_022970.3(FGFR2):c.557T>C (p.Met186Thr)	rs755793
NM_022970.3(FGFR2):c.696A>G (p.Val232=)	rs1047100
NM_022970.3(FGFR2):c.748+18C>T	rs377269009
NM_022970.3(FGFR2):c.831C>T (p.Val277=)	rs886038255
NM_022970.3(FGFR2):c.939+11T>C	rs145303463

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