ClinVar Miner

List of variants in gene CELSR1 reported as benign for not provided

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_001378328.1(CELSR1):c.1275C>G (p.Leu425=) rs1009154 0.92493
NM_001378328.1(CELSR1):c.1230C>T (p.Ser410=) rs1009155 0.87017
NM_001378328.1(CELSR1):c.6319A>G (p.Ile2107Val) rs4044210 0.30730
NM_001378328.1(CELSR1):c.2961G>A (p.Val987=) rs8141744 0.23018
NM_001378328.1(CELSR1):c.8842G>A (p.Gly2948Ser) rs35364389 0.22454
NM_001378328.1(CELSR1):c.214C>T (p.Arg72Trp) rs10427790 0.05598
NM_001378328.1(CELSR1):c.8826G>A (p.Thr2942=) rs6008778 0.05390
NM_001378328.1(CELSR1):c.8947C>G (p.Pro2983Ala) rs61741871 0.03273
NM_001378328.1(CELSR1):c.8961G>A (p.Pro2987=) rs28495011 0.03244
NM_001378328.1(CELSR1):c.7971A>G (p.Ala2657=) rs76868014 0.02692
NM_001378328.1(CELSR1):c.8891C>T (p.Ser2964Leu) rs6008777 0.02609
NM_001378328.1(CELSR1):c.6366T>C (p.Asn2122=) rs115467657 0.02005
NM_001378328.1(CELSR1):c.6411G>A (p.Ala2137=) rs35091156 0.01860
NM_001378328.1(CELSR1):c.1759A>G (p.Ile587Val) rs34141466 0.01752
NM_001378328.1(CELSR1):c.4809C>T (p.Val1603=) rs61737818 0.01700
NM_001378328.1(CELSR1):c.5059+9C>T rs145584601 0.01668
NM_001378328.1(CELSR1):c.6078C>T (p.Pro2026=) rs61737809 0.01494
NM_001378328.1(CELSR1):c.5059+10C>T rs59224842 0.01491
NM_001378328.1(CELSR1):c.7194C>T (p.Phe2398=) rs113616457 0.00952
NM_001378328.1(CELSR1):c.6134C>T (p.Thr2045Met) rs12169391 0.00936
NM_001378328.1(CELSR1):c.8238C>T (p.Asp2746=) rs74699704 0.00921
NM_001378328.1(CELSR1):c.4572C>T (p.Asp1524=) rs34897600 0.00912
NM_001378328.1(CELSR1):c.5622C>T (p.Asp1874=) rs34107040 0.00877
NM_001378328.1(CELSR1):c.8988C>G (p.Ala2996=) rs77489567 0.00873
NM_001378328.1(CELSR1):c.3055G>T (p.Ala1019Ser) rs61737811 0.00781
NM_001378328.1(CELSR1):c.8107G>A (p.Val2703Met) rs75983687 0.00766
NM_001378328.1(CELSR1):c.2274C>T (p.Tyr758=) rs28613988 0.00760
NM_001378328.1(CELSR1):c.8319G>A (p.Lys2773=) rs34191340 0.00689
NM_001378328.1(CELSR1):c.4377A>G (p.Arg1459=) rs77948853 0.00631
NM_001378328.1(CELSR1):c.3738C>T (p.Asn1246=) rs35364113 0.00553
NM_001378328.1(CELSR1):c.2318C>T (p.Ala773Val) rs12170597 0.00529
NM_001378328.1(CELSR1):c.1776G>A (p.Ala592=) rs61737812 0.00405
NM_001378328.1(CELSR1):c.5085C>T (p.Ser1695=) rs61737821 0.00400
NM_001378328.1(CELSR1):c.1036A>T (p.Thr346Ser) rs142090496 0.00148
NM_001378328.1(CELSR1):c.1065G>A (p.Gln355=) rs138032863 0.00144
NM_001378328.1(CELSR1):c.4683T>C (p.Asp1561=) rs147486726 0.00130
NM_001378328.1(CELSR1):c.1881C>T (p.Asp627=) rs56207834 0.00118
NM_001378328.1(CELSR1):c.6846C>T (p.Ser2282=) rs146846163 0.00083
NM_001378328.1(CELSR1):c.8415C>T (p.Ser2805=) rs138188369 0.00070
NM_001378328.1(CELSR1):c.5310C>T (p.Thr1770=) rs144157544 0.00065
NM_001378328.1(CELSR1):c.2196C>A (p.Arg732=) rs149287307 0.00063
NM_001378328.1(CELSR1):c.8367C>T (p.Asp2789=) rs147530261 0.00055
NM_001378328.1(CELSR1):c.3240G>A (p.Pro1080=)
NM_001378328.1(CELSR1):c.4356C>T (p.Phe1452=)
NM_001378328.1(CELSR1):c.4428C>T (p.Asn1476=)
NM_001378328.1(CELSR1):c.4517_4518insCGCAGGTGGGGCCTTC (p.Glu1509fs) rs768467194
NM_001378328.1(CELSR1):c.477G>T (p.Pro159=)
NM_001378328.1(CELSR1):c.5702-8C>T
NM_001378328.1(CELSR1):c.5861C>T (p.Pro1954Leu)
NM_001378328.1(CELSR1):c.6250+177C>T
NM_001378328.1(CELSR1):c.6372G>T (p.Thr2124=) rs34751339
NM_001378328.1(CELSR1):c.6877G>A (p.Glu2293Lys)
NM_001378328.1(CELSR1):c.6935G>C (p.Arg2312Pro) rs7287089
NM_001378328.1(CELSR1):c.7179C>A (p.Pro2393=) rs140558529
NM_001378328.1(CELSR1):c.7955C>A (p.Ser2652Tyr)
NM_001378328.1(CELSR1):c.8051A>G (p.Tyr2684Cys)
NM_001378328.1(CELSR1):c.8126G>A (p.Arg2709Gln)
NM_001378328.1(CELSR1):c.8813C>A (p.Pro2938Gln)
NM_001378328.1(CELSR1):c.8886_8897del (p.Arg2965_Ser2968del) rs375307146
NM_001378328.1(CELSR1):c.9042TAATGAAACTTCAATTTGAACCATCAG[1] (p.Gly3013_Ter3020=) rs576512903

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