List of variants in gene HRAS, LRRC56 studied for B-cell neoplasm

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

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.181C>G (p.Gln61Glu)	rs28933406
NM_005343.4(HRAS):c.182A>C (p.Gln61Pro)	rs121913233
NM_005343.4(HRAS):c.182A>T (p.Gln61Leu)	rs121913233
NM_005343.4(HRAS):c.34G>A (p.Gly12Ser)	rs104894229
NM_005343.4(HRAS):c.34G>T (p.Gly12Cys)	rs104894229
NM_005343.4(HRAS):c.35G>C (p.Gly12Ala)	rs104894230
NM_005343.4(HRAS):c.37G>C (p.Gly13Arg)	rs104894228
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_005343.4(HRAS):c.38G>C (p.Gly13Ala)	rs104894226
NM_005343.4(HRAS):c.38G>T (p.Gly13Val)	rs104894226
NM_005343.4(HRAS):c.436G>A (p.Ala146Thr)	rs104894231
NM_005343.4(HRAS):c.436G>C (p.Ala146Pro)	rs104894231
NM_005343.4(HRAS):c.437C>T (p.Ala146Val)	rs121917759

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