Krtdap Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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13 records found for search term Krtdap

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156061485	CV2239991	single nucleotide variant	NM_207392.3(KRTDAP):c.11C>T (p.Pro4Leu)	not specified [RCV004110781]	uncertain significance	19	35490432	35490432	Human		name
401879455	CV2785097	single nucleotide variant	NM_207392.3(KRTDAP):c.56C>T (p.Ser19Phe)	not specified [RCV004355110]	uncertain significance	19	35490387	35490387	Human		name
405808298	CV3266127	single nucleotide variant	NM_207392.3(KRTDAP):c.73C>G (p.Leu25Val)	not specified [RCV004407009]	uncertain significance	19	35490370	35490370	Human		name
407480719	CV3455967	single nucleotide variant	NM_207392.3(KRTDAP):c.31C>T (p.Leu11Phe)	not specified [RCV004639787]	uncertain significance	19	35490412	35490412	Human		name
156370590	CV2204252	single nucleotide variant	NM_207392.3(KRTDAP):c.113C>T (p.Ala38Val)	not specified [RCV004079087]	uncertain significance	19	35488815	35488815	Human		name
155968728	CV2213210	single nucleotide variant	NM_207392.3(KRTDAP):c.170C>T (p.Ala57Val)	not specified [RCV004085436]	uncertain significance	19	35488484	35488484	Human		name
155942739	CV2225865	single nucleotide variant	NM_207392.3(KRTDAP):c.226A>C (p.Lys76Gln)	not specified [RCV004103262]	uncertain significance	19	35487747	35487747	Human		name
401770930	CV2726305	single nucleotide variant	NM_207392.3(KRTDAP):c.140C>G (p.Pro47Arg)	not specified [RCV004326747]	uncertain significance	19	35488690	35488690	Human		name
401894366	CV2780828	single nucleotide variant	NM_207392.3(KRTDAP):c.268G>A (p.Gly90Arg)	not specified [RCV004352146]	uncertain significance	19	35487460	35487460	Human		name
405808294	CV3266125	single nucleotide variant	NM_207392.3(KRTDAP):c.145C>G (p.Leu49Val)	not specified [RCV004407007]	uncertain significance	19	35488685	35488685	Human		name
405808296	CV3266126	single nucleotide variant	NM_207392.3(KRTDAP):c.188T>C (p.Phe63Ser)	not specified [RCV004407008]	uncertain significance	19	35488466	35488466	Human		name
407480715	CV3455965	single nucleotide variant	NM_207392.3(KRTDAP):c.151A>G (p.Ile51Val)	not specified [RCV004639786]	uncertain significance	19	35488679	35488679	Human		name
407460172	CV3455966	single nucleotide variant	NM_207392.3(KRTDAP):c.243C>A (p.Asn81Lys)	not specified [RCV004633791]	uncertain significance	19	35487730	35487730	Human		name