All variants in the HBS1L gene

Information The variants shown are described using the NM_006620.3 transcript reference sequence.

31 entries on 1 page. Showing entries 1 - 31.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. - c.-61557A>G r.(=) p.(=) Substitution g.135437386T>C C-C So,et al;dbSNP HBS1L_000029 132/238 - Likely benign Qi Ming
./. - c.-59672A>G r.(=) p.(=) Substitution g.135435501T>C Yi S,et al;dbSNP HBS1L_000015 - - Likely benign Qi Ming
./. - c.-59342C>T r.(=) p.(=) Substitution g.135435171G>A C-C So,et al;dbSNP HBS1L_000028 130/238 - Likely benign Qi Ming
./. - c.-56723A>G r.(=) p.(=) Substitution g.135432552T>C Yi S,et al;dbSNP HBS1L_000011 - - Likely benign Qi Ming
./. - c.-56232T>C r.(=) p.(=) Substitution g.135432061A>G C-C So,et al;dbSNP HBS1L_000027 125/238 - Likely benign Qi Ming
./. - c.-55811A>G r.(=) p.(=) Substitution g.135431640T>C C-C So,et al;dbSNP HBS1L_000007 98/238 - Likely benign Qi Ming
./. - c.-55811A>G r.(=) p.(=) Substitution g.135431640T>C Yi S,et al;dbSNP HBS1L_000007 - - Likely benign Qi Ming
./. - c.-51988C>T r.(=) p.(=) Substitution g.135427817G>A C-C So,et al;dbSNP HBS1L_000006 99/238 - Likely benign Qi Ming
./. - c.-51330A>G r.(=) p.(=) Substitution g.135427159T>C Yunyan He,et al ;dbSNP HBS1L_000026 16/312 - Likely benign Qi Ming
./. - c.-51315G>T r.(=) p.(=) Substitution g.135427144C>A C-C So,et al;dbSNP HBS1L_000025 100/238 - Likely benign Qi Ming
./. - c.-50744T>C r.(=) p.(=) Substitution g.135426573A>G Yi S,et al;dbSNP HBS1L_000005 - - Likely benign Qi Ming
./. - c.-50729T>A r.(=) p.(=) Substitution g.135426558A>T C-C So,et al;dbSNP HBS1L_000004 100/238 - Likely benign Qi Ming
./. - c.-48895delA r.(=) p.(=) Deletion g.135424724delT Yi S,et al;dbSNP HBS1L_000010 - - Likely benign Qi Ming
./. - c.-48350G>C r.(=) p.(=) Substitution g.135424179C>G Yunyan He,et al ;dbSNP HBS1L_000003 - - Likely benign Qi Ming
./. - c.-47583C>T r.(=) p.(=) Substitution g.135423412G>A C-C So,et al;dbSNP HBS1L_000024 130/238 - Likely benign Qi Ming
./. - c.-46467T>A r.(=) p.(=) Substitution g.135422296A>T C-C So,et al;dbSNP HBS1L_000002 101/238 - Likely benign Qi Ming
./. - c.-46467T>A r.(=) p.(=) Substitution g.135422296A>T dbSNP HBS1L_000002 - - - Qianqian Zhang
./. - c.-45239delA r.(=) p.(=) Deletion g.135421068delT Yi S,et al;dbSNP HBS1L_000016 - - Likely benign Qi Ming
./. - c.-43859A>G r.(=) p.(=) Substitution g.135419688T>C Lai Y,et al;dbSNP HBS1L_000020 - - Likely benign Qi Ming
?/. - c.-43802T>C r.(=) p.(=) Substitution g.135419631A>G Lai Y,et al;dbSNP HBS1L_000018 - - Likely benign Qi Ming
./. - c.-43425A>G r.(=) p.(=) Substitution g.135419254T>C Yi S,et al;dbSNP HBS1L_000009 - - Likely benign Qi Ming
./. - c.-43209delG r.(=) p.(=) Deletion g.135419038delC Shang,et al;dbSNP HBS1L_000021 - - Likely benign Qi Ming
./. - c.-43209G>T r.(=) p.(=) Substitution g.135419038C>A Yi S,et al;dbSNP HBS1L_000001 - - Likely benign Qi Ming
?/. - c.-43189A>G r.(=) p.(=) Substitution g.135419018T>C Lai Y,et al; HBS1L_000019 - - Likely benign Qi Ming
./. - c.-43087T>C r.(=) p.(=) Substitution g.135418916A>G Lai Y,et al;dbSNP HBS1L_000017 - - Likely benign Qi Ming
./. - c.-42806_-42804delGTA r.(=) p.(=) Deletion g.135418633_135418635delTAC Yi S,et al;dbSNP HBS1L_000014 - - Likely benign Qi Ming
./. - c.-39379C>T r.(=) p.(=) Substitution g.135415208G>A C-C So,et al;dbSNP HBS1L_000023 157/238 - Likely benign Qi Ming
./. - c.-38380C>T r.(=) p.(=) Substitution g.135414209G>A Yi S,et al;dbSNP HBS1L_000012 - - Likely benign Qi Ming
./. - c.-35399A>G r.(=) p.(=) Substitution g.135411228T>C Lai Y,et al;dbSNP HBS1L_000022 89/238 - Likely benign Qi Ming
./. - c.-25542G>A r.(=) p.(=) Substitution g.135401371C>T Yi S,et al;dbSNP HBS1L_000013 - - Likely benign Qi Ming
./. - c.431-185T>G r.(=) p.(=) Substitution g.135324165A>C Yi S,et al;dbSNP HBS1L_000008 - - uncertain significance Qi Ming
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