ClinVar Miner

List of variants in gene COL7A1 reported as benign by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_000094.3(COL7A1):c.1098G>A (p.Gly366=) rs150776274
NM_000094.3(COL7A1):c.1383A>G (p.Val461=) rs112805032
NM_000094.3(COL7A1):c.1628G>A (p.Ser543Asn) rs76410546
NM_000094.3(COL7A1):c.1836G>T (p.Thr612=) rs151186709
NM_000094.3(COL7A1):c.2766C>T (p.Asp922=) rs201424023
NM_000094.3(COL7A1):c.3359G>A (p.Arg1120Lys) rs2228563
NM_000094.3(COL7A1):c.3889G>A (p.Glu1297Lys) rs149881350
NM_000094.3(COL7A1):c.4068C>T (p.Ile1356=) rs146913953
NM_000094.3(COL7A1):c.4222C>T (p.Arg1408Trp) rs143126677
NM_000094.3(COL7A1):c.4517G>A (p.Arg1506Gln) rs372793584
NM_000094.3(COL7A1):c.4719A>G (p.Glu1573=) rs558405095
NM_000094.3(COL7A1):c.5154+5T>C rs2854400
NM_000094.3(COL7A1):c.5307+7G>C rs116455408
NM_000094.3(COL7A1):c.5343C>T (p.Ser1781=) rs147919436
NM_000094.3(COL7A1):c.54G>C (p.Ala18=) rs35899847
NM_000094.3(COL7A1):c.5590G>A (p.Ala1864Thr) rs17080261
NM_000094.3(COL7A1):c.5778C>T (p.Leu1926=) rs113151410
NM_000094.3(COL7A1):c.5819C>T (p.Pro1940Leu) rs149267939
NM_000094.3(COL7A1):c.5988C>T (p.Ile1996=) rs146901730
NM_000094.3(COL7A1):c.6081C>T (p.Pro2027=) rs375047225
NM_000094.3(COL7A1):c.6217-6C>T rs191559835
NM_000094.3(COL7A1):c.683-8A>G rs113167762
NM_000094.3(COL7A1):c.6937-9C>G rs143589222
NM_000094.3(COL7A1):c.7008G>A (p.Gly2336=) rs117723065
NM_000094.3(COL7A1):c.7191C>A (p.Pro2397=) rs34360255
NM_000094.3(COL7A1):c.7286C>T (p.Pro2429Leu) rs2229822
NM_000094.3(COL7A1):c.7313C>G (p.Pro2438Arg) rs185142403
NM_000094.3(COL7A1):c.7353T>C (p.Pro2451=) rs139461888
NM_000094.3(COL7A1):c.7687-6C>T rs200429526
NM_000094.3(COL7A1):c.802C>T (p.Pro268Ser) rs35623035
NM_000094.3(COL7A1):c.8047-4C>T rs185429200
NM_000094.3(COL7A1):c.8504G>A (p.Arg2835His) rs139014122
NM_000094.4(COL7A1):c.1907G>T rs116005007
NM_000094.4(COL7A1):c.1985A>G (p.Gln662Arg)
NM_000094.4(COL7A1):c.3611C>T (p.Ala1204Val)
NM_000094.4(COL7A1):c.5913G>T rs754578634

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