http://identifiers.org/hco/5/GRCh38#135476964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56356126-A-C

135476995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: non coding transcript exon variant
orthologous variants: 56356157-G-C

http://identifiers.org/hco/5/GRCh38#135477043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56356205-C-A

http://identifiers.org/hco/5/GRCh38#135477416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56356572-C-A

135477432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56356588-C-T

135478189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56357266-T-G

135478536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56357821-A-G

135479128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56358343-G-A

135479332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56358512-C-T

135479675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56359157-C-G

135479675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56359157-C-T

135480316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56359698-G-A

135480539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56359874-G-A

135480567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56359895-G-T

135482233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56362177-A-G

135482692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56362603-G-T

135482998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56362898-C-T

135483118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56363032-G-A

135483135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56363049-G-A

135484558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56363940-A-G

135484880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56364293-G-A

135484880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56364293-G-T

135485692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56364798-G-A

135485799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56364893-T-C

135485862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56364968-A-T

135486188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56365828-C-T

http://identifiers.org/hco/5/GRCh38#135486349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56365962-C-A

http://identifiers.org/hco/5/GRCh38#135486416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56366023-C-A

135486489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56366107-G-C

135487022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367102-T-C

135487252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56367287-G-A

135487988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368200-G-T

135488050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368262-A-T

135488150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368333-T-G

135488240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368438-C-T

135488245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368443-A-G

135488263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368461-C-T

135488815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56368897-G-A

135489400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369468-G-A

135489470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369537-C-T

135489533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369598-C-G

135489779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369867-T-C

135489779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56369867-T-G

135490223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370275-G-A

135490344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370398-G-A

http://identifiers.org/hco/5/GRCh38#135490478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56370544-C-A

135490504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370567-T-G

135490581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370593-G-A

135490611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370623-G-C

135490616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370628-C-G

135490954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370873-C-T

135491112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56370991-T-C

135491433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371304-G-C

135491454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371333-G-A

135491459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371338-A-G

135491511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371397-A-G

135491658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371547-C-T

135491760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371654-A-G

135491778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371672-G-A

135491778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371672-G-C

135491836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371726-C-G

135491916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56371810-C-T

135492224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56372082-A-T

135493354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56372546-A-G

135493674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56373468-T-G

135493814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56373855-T-G

135494327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374309-C-T

135494384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374366-C-T

135494447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374425-C-T

135494647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374619-C-G

135494647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374619-C-T

135497213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374801-G-A

135497254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374833-C-G

135497254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374833-C-T

135497422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374994-G-C

135497844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375508-A-G

135498031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375825-T-A

135498031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375825-T-C

135498053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375847-T-A

135498690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376415-A-T

135498720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376437-A-G

135498903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376673-C-G

135498903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376673-C-T

135499398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377139-T-C

135499457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377184-T-C

http://identifiers.org/hco/5/GRCh38#135499477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56377204-A-C

135499477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377204-A-T

http://identifiers.org/hco/5/GRCh38#135499536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56377250-C-A

135499557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377271-A-G

135499557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377271-A-T

135499590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377331-C-G

135499596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377337-G-A

135499994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377726-C-T

135501850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380147-G-A

135501896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380191-G-A

135502337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380638-G-C

135502389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56380691-G-T

135506915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383207-G-T

135507225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56383541-T-C

135509123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384671-A-G

135509511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56385020-C-G

135509511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56385020-C-T

135509692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56386180-C-T

135510047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56386503-C-T

135510384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56386793-G-A

135510468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56386879-T-C

135510599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387021-T-A

135510674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387088-G-A

135510720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387131-T-C

135510845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387296-G-C

135510914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387364-T-C

135510927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387377-A-G

135511025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387473-C-G

http://identifiers.org/hco/5/GRCh38#135511065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56387517-C-A

135511157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387608-G-A

135511788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

135512080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56388173-G-A

135512080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56388173-G-T

135512486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56388579-G-A

135514394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390021-C-T

135514395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390022-T-C

135514471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390093-G-C

135514471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390093-G-T

135514490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390124-C-G

135514644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390250-A-G

135514950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390386-C-G

135514955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390391-A-G

135515012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390443-G-T

135515180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390587-G-A

http://identifiers.org/hco/5/GRCh38#135515218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56390626-C-A

135515288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390681-T-C

135515453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56390807-A-G

http://identifiers.org/hco/5/GRCh38#135515584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56390944-A-C

135527963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56392138-C-T

135528200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393223-G-A

135528218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393241-A-G

http://identifiers.org/hco/5/GRCh38#135528398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56393424-C-A

135528398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393424-C-T

135528471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393687-G-A

135528486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393701-A-G

135528609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393821-T-C

135528678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393889-G-C

135528727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393939-A-G

135528734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56393946-G-A

135529032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56394188-C-T

135531279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396195-G-A

http://identifiers.org/hco/5/GRCh38#135531839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56396379-A-C

135531839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396379-A-G

135531839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396379-A-T

http://identifiers.org/hco/5/GRCh38#135531848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56396386-C-A

135531850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396388-T-A

135531850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396388-T-C

135531850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396388-T-G

135532044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396579-T-C

135532061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396616-T-G

135532355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56396865-G-A

135532795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397279-C-T

135533533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397605-C-G

135533533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397605-C-T

135533659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397689-G-A

135533750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56397769-T-C

135533995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398007-G-A

135534000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398011-C-T

135534135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56398144-A-G

http://identifiers.org/hco/5/GRCh38#135534235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398241-C-A

135534490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398509-T-A

135534490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398509-T-G

135534761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398784-G-A

135534761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398784-G-T

135534768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398791-G-T

135534777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398805-G-A

135534777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398805-G-T

http://identifiers.org/hco/5/GRCh38#135534787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398814-C-A

135534787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398814-C-G

135534787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398814-C-T

http://identifiers.org/hco/5/GRCh38#135534795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398822-C-A

135534795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398822-C-T

http://identifiers.org/hco/5/GRCh38#135534816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398842-C-A

135534816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56398842-C-T

135534848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398873-T-C

http://identifiers.org/hco/5/GRCh38#135534854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398879-C-A

135534854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56398879-C-T

http://identifiers.org/hco/5/GRCh38#135534881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56398903-C-A

135534969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399004-C-G

135534969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399004-C-T

135535002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56399036-G-A

135535027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399061-G-A

135535052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399086-G-A

135535052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399086-G-T

135535097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399131-G-A

135535097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56399131-G-T

135535121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399173-G-A

http://identifiers.org/hco/5/GRCh38#135535153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56399205-C-A

135535153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56399205-C-T

135535178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399230-G-A

135535268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399320-G-A

135535268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399320-G-T

135535328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 56399380-C-G

135535364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 56399416-G-A

135535364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 56399416-G-T

135535430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399482-G-A

http://identifiers.org/hco/5/GRCh38#135535535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56399587-C-A

135535535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399587-C-G

135535535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399587-C-T

http://identifiers.org/hco/5/GRCh38#135535553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56399605-C-A

135535553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399605-C-T

135535576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56399628-C-T

135535625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399677-T-A

135535625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399677-T-G

135535627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56399679-G-A

135535627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56399679-G-T

http://identifiers.org/hco/5/GRCh38#135535703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56399757-C-A

135535703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399757-C-T

135535826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399853-G-A

135535826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399853-G-C

135535826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399853-G-T

135535833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399860-T-A

135535833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56399860-T-C

135535907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56399936-G-A

135535907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56399936-G-T

135535956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56399985-G-A

135535956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56399985-G-T

135536040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56400068-G-A

135536040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56400068-G-T

135536258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400289-C-G

135536308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400343-C-T

135536361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400394-G-T

http://identifiers.org/hco/5/GRCh38#135536374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56400407-C-A

http://identifiers.org/hco/5/GRCh38#135536595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56400512-C-A

135536595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400512-C-T

135537003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400791-C-T

135537137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400918-A-G

135537147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56400931-G-T

135537331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401102-C-T

135537584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401299-C-T

135537789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401532-T-C

135537825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401571-A-T

http://identifiers.org/hco/5/GRCh38#135537828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56401574-C-A

135538010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401707-A-T

135538303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56401936-G-C

135538659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402192-G-T

135538861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402368-C-T

135538906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402413-C-G

135539157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402656-G-A

135539172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402671-C-T

135539195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402678-C-T

135539205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402688-G-T

http://identifiers.org/hco/5/GRCh38#135539284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56402776-A-C

135539618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403106-T-G

135540075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403457-G-A

135540482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403646-G-A

135540964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403917-C-T

135541828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404649-G-A

135542057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404883-G-A

135542087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404913-C-T

http://identifiers.org/hco/5/GRCh38#135542128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56404942-C-A

135542128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404942-C-T

135542140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404954-G-A

135542178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56404992-T-C

135542335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405193-C-T

135542600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405457-C-T

http://identifiers.org/hco/5/GRCh38#135542615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56405472-C-A

135543630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406421-C-T

135544157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406799-C-T

135544519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406905-C-T

135544601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406976-C-G

135544602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406977-T-C

135544646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407037-G-C

135544674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407064-G-C

135544676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407066-C-T

135544677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407067-G-A

http://identifiers.org/hco/5/GRCh38#135544910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56407280-C-A

135545064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407424-A-T

135545133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407493-C-G

135545217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407579-T-C

135545346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407717-G-T

http://identifiers.org/hco/5/GRCh38#135545423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56407781-C-A

135545423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56407781-C-T

http://identifiers.org/hco/5/GRCh38#135545783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56408028-C-A

135546024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56408095-C-T

135546858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56408824-A-T

135547693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56409978-G-A

135547752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410035-G-A

135547752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410035-G-C

135547816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410098-G-T

135548150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410439-T-G

135548173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56410462-G-A

135548532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56411479-C-G

135548532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56411479-C-T

135548548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56411494-G-A

135549950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413526-C-T

135552006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56414430-G-A

http://identifiers.org/hco/5/GRCh38#135552021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56414445-A-C

135557186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417994-C-T

135557292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418137-T-A

135557296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418141-C-T

135560774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56427244-T-C

135560805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56427275-T-C

135560834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56427306-T-C

135560903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56427378-T-A

135561023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56427481-G-A

135561291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427694-A-G

135561455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427807-G-T

135561523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427868-G-A

135561562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56427895-C-T

135561903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56428091-C-G

135561903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56428091-C-T

135562056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56428243-G-A

135564264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430267-C-T

135564278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430281-C-T

135565119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430841-G-T

135565134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430851-A-G

135565340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56430973-T-C

http://identifiers.org/hco/5/GRCh38#135565372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56431003-A-C

135565566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56431160-T-C

135565728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56431305-C-G

http://identifiers.org/hco/5/GRCh38#135570479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56436247-C-A

135570501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436269-C-T

135570517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436284-T-C

135570602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56436355-C-T

135570795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436576-G-A

135570795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436576-G-T

http://identifiers.org/hco/5/GRCh38#135570859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56436655-C-A

135570859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436655-C-T

135570879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436675-C-T

135571030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436809-T-A

135571127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436915-T-C

135571128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56436916-G-T

135571332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437107-G-T

135571398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437173-G-A

135571398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437173-G-T

135571433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437208-A-G

135571621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437409-G-A

135571621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437409-G-T

135571718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437503-T-A

135571718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437503-T-C

135571718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437503-T-G

135571790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437542-T-A

135571790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437542-T-C

135571790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437542-T-G

135571800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437552-T-A

135571800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437552-T-C

135571800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437552-T-G

http://identifiers.org/hco/5/GRCh38#135571805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56437557-A-C

135571805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437557-A-G

135571805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56437557-A-T

135571905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56437659-C-T

135572971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438476-A-G

135573055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438605-G-C

135573066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438616-A-G

135573132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438688-G-C

135573216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438757-T-C

135573230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438771-C-T

135573314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56438871-C-G

135573582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439111-C-T

135573602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439131-C-T

135573657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439186-G-T

135573869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439336-A-G

135573873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439340-G-A

135573873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439340-G-T

135574025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439470-G-A

135574104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439533-A-G

135574208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439620-C-T

135574315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56439978-G-A

http://identifiers.org/hco/5/GRCh38#135574343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56440007-C-A

135574343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440007-C-T

135574363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440027-A-G

http://identifiers.org/hco/5/GRCh38#135574436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56440099-A-C

135574436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440099-A-T

http://identifiers.org/hco/5/GRCh38#135574506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56440167-C-A

135574506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440167-C-G

135574506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440167-C-T

135574554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440240-A-T

135574557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440255-A-G

135574560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440258-G-T

135574563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440261-G-A

135574568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440270-G-A

135574568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440270-G-T

135574685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 56440387-G-A

135574778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440450-G-T

135574791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440460-G-A

135574791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440460-G-T

http://identifiers.org/hco/5/GRCh38#135574834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56440489-C-A

135574895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440539-G-A

135574909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440544-G-A

http://identifiers.org/hco/5/GRCh38#135575036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56440621-C-A

135575155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440701-G-A

135575156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440702-C-G

135575282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56440814-C-T

135576542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56441851-T-C

http://identifiers.org/hco/5/GRCh38#135576703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56442122-A-C

135576703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442122-A-G

135576840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442331-G-C

135576992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442434-T-C

135577039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442475-C-G

135577067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442500-G-A

135577138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442562-T-C

135577292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442665-C-T

135577320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442698-C-T

135577409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56442760-G-T

135577885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443223-A-G

135578143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443437-C-T

135578298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443546-G-T

http://identifiers.org/hco/5/GRCh38#135578354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56443584-C-A

135578354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443584-C-T

135578367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443597-C-T

135578576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443779-G-A

135578576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443779-G-T

135578592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443795-C-G

135578592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443795-C-T

http://identifiers.org/hco/5/GRCh38#135578612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56443816-C-A

135578612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443816-C-G

http://identifiers.org/hco/5/GRCh38#135578618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56443832-A-C

135578618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443832-A-G

135578618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443832-A-T

135578659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443872-G-A

135578659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443872-G-T

135578661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443874-T-C

135578661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56443874-T-G

135578707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 56443915-G-A

135578707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 56443915-G-C

135578707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 56443915-G-T

135578865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444072-C-T

http://identifiers.org/hco/5/GRCh38#135578903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444110-C-A

http://identifiers.org/hco/5/GRCh38#135578919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444126-C-A

135578919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444126-C-T

135578942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444149-T-A

135578942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444149-T-C

http://identifiers.org/hco/5/GRCh38#135578961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444171-C-A

135578961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444171-C-T

135578966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444176-T-A

135578966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444176-T-C

http://identifiers.org/hco/5/GRCh38#135578994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444204-C-A

135578994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56444204-C-T

http://identifiers.org/hco/5/GRCh38#135579263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444472-C-A

135579370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56444554-G-A

135579447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444617-T-C

135579447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444617-T-G

http://identifiers.org/hco/5/GRCh38#135579475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444645-C-A

135579475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444645-C-T

135579482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444652-G-A

http://identifiers.org/hco/5/GRCh38#135579490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56444660-A-C

135579490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444660-A-G

135579504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444688-G-A

135579504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56444688-G-T

135579718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444855-G-A

135579718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444855-G-C

135579718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444855-G-T

135579786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56444924-G-A

135580016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56445129-G-T

135580375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56445469-G-A

http://identifiers.org/hco/5/GRCh38#135580465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56445555-C-A

135580560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56445644-G-A

135580566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56445650-G-A

135580628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56445699-G-A

http://identifiers.org/hco/5/GRCh38#135584095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56449120-C-A

135584095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449120-C-T

135584110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449127-G-A

135584150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449169-T-G

135584225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449244-A-G

135584406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449394-T-C

http://identifiers.org/hco/5/GRCh38#135584463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56449441-A-C

135584559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449499-G-T

135584710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449758-T-G

135584716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56449764-C-T

135584979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450076-T-C

135585087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450157-C-T

135585123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450191-G-A

135585304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450335-G-T

135585733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450738-C-G

135585749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450755-T-C

135585765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450771-G-A

135585807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450856-G-A

135585916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56450947-C-T

135586319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451279-T-C

135586384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451344-G-A

135586409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451369-A-T

135586444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451404-C-T

135586486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451446-G-A

135586506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451467-G-A

135586560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451508-C-T

135586603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451547-A-G

135586653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451615-G-A

135586794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451763-T-C

135586809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56451779-T-C

135587245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452277-C-T

135587468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452567-A-G

135587622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452732-C-G

135587756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452836-C-T

135587858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56452937-G-A

135588298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453304-C-G

135588453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453396-C-T

135588517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453449-G-A

135588746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453581-T-A

135588770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453596-T-G

135588915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453726-C-T

135589132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56453977-G-A

135589239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454094-T-C

135589279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454126-G-A

135589584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454404-T-G

135589600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454420-T-C

135590212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454662-C-T

135590264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454705-C-T

http://identifiers.org/hco/5/GRCh38#135590307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56454748-C-A

135590315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454752-G-A

135590321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56454758-G-A

135590623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56455064-G-T

http://identifiers.org/hco/5/GRCh38#135590625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56455066-C-A

135590625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56455066-C-T

135590706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56455150-C-T

135593181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56455793-A-G

135593405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456020-C-T

135593415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456029-C-T

135593430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456044-G-A

135593476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456086-G-A

135593646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456226-G-A

135594055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456348-C-G

135594055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456348-C-T

135594089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456381-G-C

135594093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456385-G-C

135594388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456689-G-A

135594499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456778-T-C

135594746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56456995-C-G

135594871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457119-C-T

135595414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457938-C-T

135595416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56457940-G-A

http://identifiers.org/hco/5/GRCh38#135596444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56459135-A-C

135596533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459247-C-G

135596541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459255-G-A

135596682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459398-C-T

135596711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459448-T-G

135596786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459584-C-T

135596797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459597-C-T

135596878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459670-C-T

135596892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459686-G-T

135596907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459701-G-T

135597009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459793-A-T

135597029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459810-T-A

135597126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56459938-A-G

http://identifiers.org/hco/5/GRCh38#135599889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56460277-C-A

135599908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460294-G-C

135599969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460352-T-A

135599992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460380-T-A

135600099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460459-A-T

135600112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56460472-A-G

135600441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461458-G-T

135601601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56461510-C-T

http://identifiers.org/hco/5/GRCh38#135601871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56462140-C-A

135601875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462144-G-A

135601997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462263-C-T

http://identifiers.org/hco/5/GRCh38#135602237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56462379-A-C

135602275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462415-A-G

135602621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462592-T-C

http://identifiers.org/hco/5/GRCh38#135602633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56462604-C-A

135602633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462604-C-T

135602645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56462617-G-T

135603306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56463066-C-T

135603458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56463202-C-T

135603690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56463444-G-A

135603814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56463752-G-A

135603848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56463864-C-T

135603933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464017-G-A

135604013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464114-T-C

135604079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464184-A-G

135604246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464356-C-T

http://identifiers.org/hco/5/GRCh38#135604371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56464456-C-A

135604768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464747-T-A

135604909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464857-T-A

135604909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464857-T-C

135604963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56464910-G-A

135605068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465010-C-G

135605209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465156-G-A

135606159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468370-A-G

135606428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469262-T-G

135606844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469670-G-A

135606844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469670-G-T

135607041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469870-T-C

135607082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469910-A-G

135607207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470016-C-G

135607207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470016-C-T

135607284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470081-A-T

135607332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470444-A-G

135607614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470737-A-G

http://identifiers.org/hco/5/GRCh38#135607770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56471217-C-A

135607776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471223-G-A

135607811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471256-G-C

135608408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471708-A-G

135608411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471711-G-A

135608460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471751-G-C

135608841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472016-G-A

135608841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472016-G-T

135608940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472106-T-C

135609152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472280-G-A

135609152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472280-G-T

135609162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472290-C-T

135609267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472392-C-T

135609292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472407-G-A

135609309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472424-G-A

135609309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472424-G-T

135609334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472451-T-C

http://identifiers.org/hco/5/GRCh38#135609349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56472460-C-A

135609394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472489-G-A

135609488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472557-A-G

135609494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472563-G-T

135609521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472583-A-G

http://identifiers.org/hco/5/GRCh38#135609603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56472632-C-A

135609609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56472638-G-T

135609954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473588-C-T

135610094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473730-A-G

135610195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473829-C-T

135610245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473879-G-T

135610452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474091-T-C

135610546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474186-C-T

135610579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474221-T-C

135610681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474315-C-T

135610877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474507-A-T

135611890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475372-C-T

135611989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475468-A-G

135612054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475533-T-C

135612189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475666-A-G

135612195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56475672-G-T

http://identifiers.org/hco/5/GRCh38#135621614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56476448-A-C

135621724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56476514-G-A

135621846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56476633-T-C

135622473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477224-G-A

135622611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477369-T-C

135622611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477369-T-G

135622650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477408-T-C

135623102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477802-C-T

135623289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56477973-C-G

135623461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478158-G-C

135623751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478372-T-C

135623786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478449-C-T

135623951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478617-T-C

135624017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478679-G-A

135624067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478728-G-A

135624094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478755-T-A

135624235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478902-G-A

135624264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56478940-G-A

135624540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56479197-A-G

http://identifiers.org/hco/5/GRCh38#135625311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56479922-A-C

http://identifiers.org/hco/5/GRCh38#135628795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56480639-C-A

135629078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480911-G-T

135629098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56480930-T-C

135629334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56481186-A-G

135629359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56481211-T-C

135629373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56481225-A-G

135629446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56481280-G-T

135629450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56481284-C-T

135629474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481306-G-A

135629474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481306-G-T

135629510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481339-C-T

135629586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481404-G-A

135630032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56481755-G-T

135630684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56482301-A-T

135630745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56482368-G-T

http://identifiers.org/hco/5/GRCh38#135631078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56482760-C-A

135631330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56482972-G-C

135631591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483200-G-A

135631591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483200-G-C

135631628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483237-T-C

135631722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483351-A-G

135631751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483378-T-A

135631808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483587-G-A

135631848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483622-A-T

135631904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483662-A-G

135631983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483754-G-A

135632165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56483913-G-A

135632308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484053-G-A

135632571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484700-G-C

135632636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484769-G-C

135632858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56484992-T-C

135633056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485193-A-G

http://identifiers.org/hco/5/GRCh38#135633075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56485212-C-A

135633075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485212-C-T

135633109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485242-C-G

135633161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485289-G-A

135633161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485289-G-C

135633161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485289-G-T

135633394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485499-G-A

135633489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485598-G-A

135633603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485696-T-C

135633637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485719-C-T

http://identifiers.org/hco/5/GRCh38#135633638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56485720-C-A

135633823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485908-G-A

135633832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56485918-A-G

http://identifiers.org/hco/5/GRCh38#135634947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56486130-C-A

135634947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56486130-C-T

135635059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486241-C-T

135635172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486307-G-A

135635554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486629-C-T

135635603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486674-A-G

135635742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486784-G-A

135635868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486905-C-G

135635868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56486905-C-T

135636053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56487097-G-A

135636343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488110-G-C

135636542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488294-G-A

135636602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488352-G-A

135637013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56488749-C-T

135637109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489082-T-C

135638312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489642-G-T

135638340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489672-T-C

135638435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489754-T-G

135638535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56489840-T-A

http://identifiers.org/hco/5/GRCh38#135638829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56490088-A-C

135638905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56490158-A-G

135639336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56490715-A-T

135639438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56490783-T-C

135639623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491032-A-G

135639715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491125-A-G

135639800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491192-C-T

135639852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491244-C-T

135639871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56491259-C-G

135641714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492089-C-T

135641732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492107-C-T

135641808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56492183-C-G

135641808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56492183-C-T

135641830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492194-C-T

135641852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492216-C-T

135641855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492219-A-T

135642190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56492568-G-C

135642190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56492568-G-T

135642437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492792-G-T

135642605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492951-T-C

135642716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493062-G-T

135642778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493115-C-G

135642879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493193-G-C

135643100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493358-A-G

135643164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493418-T-C

135643227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493480-C-T

135643261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493517-A-G

135643285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493594-G-A

135643285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493594-G-T

135643406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493712-C-T

http://identifiers.org/hco/5/GRCh38#135643453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56493768-C-A

135643514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493839-A-G

135643668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56493992-T-A

135643744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494066-C-T

http://identifiers.org/hco/5/GRCh38#135643795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56494113-C-A

135643796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494114-T-C

135644243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494401-G-A

135644253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494409-G-A

135644272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494428-G-A

135644305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494458-G-A

135644364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494507-G-A

135644371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494514-G-A

135644380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494523-G-T

135644389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494532-A-G

135644401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494544-G-A

135644401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494544-G-T

135644823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494932-C-T

http://identifiers.org/hco/5/GRCh38#135644953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56494957-A-C

http://identifiers.org/hco/5/GRCh38#135644996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56494982-C-A

135644996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494982-C-T

135644997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56494983-G-A

135645144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495102-C-T

135645145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495103-C-T

135645153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495111-A-G

135645360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495309-A-G

135645498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495512-C-G

135645775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495774-T-C

135645791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495790-C-G

135645875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495881-C-T

135645927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495926-G-A

135645985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495976-A-G

135645985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495976-A-T

135646042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56495998-G-A

135646082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496037-T-C

135646176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496130-G-A

135646241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496170-G-A

http://identifiers.org/hco/5/GRCh38#135646688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56496528-A-C

135646688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496528-A-G

135646688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496528-A-T

135646689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496529-G-A

135646689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496529-G-C

135646689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496529-G-T

135646694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496534-T-A

135646694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496534-T-G

135646726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496566-G-A

135646731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496571-A-T

135646870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56496651-A-G

135647698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498479-T-C

135648125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498846-G-A

135648185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56498893-C-T

135648376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499008-C-T

http://identifiers.org/hco/5/GRCh38#135648523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56499151-A-C

135648576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56499188-C-T

135648784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56499439-T-C

135648986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56499631-G-T

135649113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56499755-C-G

135649239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56499856-A-T

135649497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500069-G-T

135649630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500168-G-A

135649630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500168-G-T

135649633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500171-G-A

135649633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500171-G-T

http://identifiers.org/hco/5/GRCh38#135649644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56500182-C-A

135649699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500232-G-A

135649699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500232-G-C

135649699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500232-G-T

135649716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500241-T-C

135649716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500241-T-G

135649747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500267-A-G

135649808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500312-G-T

135649819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500323-G-T

135649820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500324-G-A

135649820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500324-G-T

135649925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500394-G-A

135649925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500394-G-T

135650030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500489-G-A

135650057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500511-A-G

135650058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500512-T-G

135650095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56500551-C-T

135650312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501372-G-T

135650315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501375-T-A

135650315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501375-T-G

135650373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501434-G-A

135650420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501482-G-A

135650420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501482-G-T

135650512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56501572-C-G

http://identifiers.org/hco/5/GRCh38#135650581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56501609-C-A

135650633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56501644-C-T

135650904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56501875-A-G

135650912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56501887-C-T

135651059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502036-T-C

135651157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502129-G-A

135651366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502283-C-T

135651464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502382-C-T

135651782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502680-T-A

135651864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502765-A-G

http://identifiers.org/hco/5/GRCh38#135651941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56502806-C-A

135651941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502806-C-T

135651944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56502809-A-T

135652209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503051-C-T

135652217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503059-C-T

http://identifiers.org/hco/5/GRCh38#135652235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56503065-C-A

135652296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503107-T-G

135652560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503482-G-A

135652618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56503510-A-G

135653431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504362-G-T

135653499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56504432-G-C

135653890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56505798-G-A

135653919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56505825-G-C

135653920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56505826-G-A

135654021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56505942-A-T

135654810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56506685-C-T

135655230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507106-T-C

135655269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507143-G-A

135655455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507323-G-A

http://identifiers.org/hco/5/GRCh38#135655480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56507347-C-A

135655527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507392-C-T

http://identifiers.org/hco/5/GRCh38#135655597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56507454-C-A

135655723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507585-C-T

135655740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56507602-T-C

http://identifiers.org/hco/5/GRCh38#135655969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56507852-C-A

135656386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508235-G-T

135656594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508372-T-A

135656852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508801-G-A

135656911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508860-C-G

135656982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56508934-A-G

135662128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56510874-G-A

135662414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511162-A-G

135662608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511354-C-T

135662878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511665-G-A

135662993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511793-A-G

135663051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511866-C-G

135663085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56511909-T-C

135663318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56512102-A-G

135663378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56512154-A-G

135663554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56512319-C-T

135666201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514028-T-C

135666209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514032-T-G

135666273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514096-T-G

135666358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514183-T-C

135666365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514190-T-G

135666375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514200-A-G

135666556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514339-T-C

135666642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514399-T-A

135666643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514400-G-T

135666733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514451-A-G

135666778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514476-A-G

135666904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514603-C-T

135667083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514785-T-C

135667108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514811-A-G

135667134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514837-G-A

135667153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514857-T-G

135667171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514875-G-C

135667738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514966-C-T

135667758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56514986-A-G

135667825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56515050-A-G

135668343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516654-A-G

135668497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56516795-T-C

http://identifiers.org/hco/5/GRCh38#135668891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56517179-C-A

135668921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517209-A-G

135669354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517285-C-G

135669386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517317-G-T

135669738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517668-A-G

135669801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517729-C-T

135669970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56517864-G-C

135670133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518023-G-T

135670218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518106-G-A

135670231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518119-G-A

135670416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518311-T-A

135670429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518331-G-T

135670568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518466-G-A

135670629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518528-T-A

135670713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518624-G-A

135670713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518624-G-T

135670729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56518638-C-T

135671539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519353-G-T

135671616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519452-A-G

http://identifiers.org/hco/5/GRCh38#135671631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56519468-C-A

135671632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519469-A-G

135671632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519469-A-T

135671633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519470-C-G

135671660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56519497-G-C

135671660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56519497-G-T

http://identifiers.org/hco/5/GRCh38#135671738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56519572-C-A

135671837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519667-G-T

http://identifiers.org/hco/5/GRCh38#135671864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56519695-C-A

135671864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519695-C-T

135671993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56519815-C-T

135672516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56520349-G-A

135672607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56520440-G-T

135672683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56520516-T-A

135682370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56523952-C-G

http://identifiers.org/hco/5/GRCh38#135682438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56524008-C-A

135682679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56524134-G-A

135682713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56524151-A-G

http://identifiers.org/hco/5/GRCh38#135682824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56524265-C-A

135682824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56524265-C-T

135682989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56524830-G-A

135682989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56524830-G-C

135683369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525179-C-T

135683390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525207-A-G

135683584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525400-T-A

135683884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525684-T-C

135683920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56525753-G-A

135687665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526462-T-A

135687944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526734-T-A

135688001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526823-C-T

135688018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526840-C-T

http://identifiers.org/hco/5/GRCh38#135688023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56526860-A-C

http://identifiers.org/hco/5/GRCh38#135688037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56526874-C-A

135688037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526874-C-T

135688038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526875-C-G

135688047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526884-G-C

135688047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56526884-G-T

135688256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527045-T-G

135688266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527055-C-T

135688312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527091-G-T

http://identifiers.org/hco/5/GRCh38#135688751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56527474-C-A

http://identifiers.org/hco/5/GRCh38#135689067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56527609-A-C

135689279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527786-A-G

135689285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56527792-T-G

135689957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528212-C-T

135689974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528225-G-A

http://identifiers.org/hco/5/GRCh38#135690047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56528283-C-A

135690822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528917-G-A

135690822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528917-G-C

135690824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528919-G-A

135690840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528933-G-T

135690846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528939-A-G

135690922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529003-A-G

135691006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529076-A-G

135691055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529117-T-C

135691318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529374-C-G

135691605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529624-T-A

135691781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531385-C-G

135692188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531735-T-G

135692191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531738-G-A

135692196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531743-T-C

135692261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531815-G-C

135692271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531825-A-T

135692294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531852-G-A

135692294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531852-G-T

http://identifiers.org/hco/5/GRCh38#135692300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56531858-C-A

135692525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532180-A-G

135692614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532268-C-T

135692679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532335-G-C

135692906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532557-G-T

135693356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533579-G-T

135693582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533781-C-G

135693792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533915-T-G

135693874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533996-G-A

135694498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534574-C-T

http://identifiers.org/hco/5/GRCh38#135694913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56534633-C-A

135694921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534641-G-C

135695087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534790-C-T

135695761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535376-A-G

135695903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535508-C-G

135695917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535522-G-C

135696576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535609-G-T

135696601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535634-T-C

http://identifiers.org/hco/5/GRCh38#135696760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56535748-C-A

135696760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535748-C-T

135696880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535860-G-A

135696989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535971-T-C

135697003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535985-A-G

135697332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536337-G-C

135697368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536370-T-G

135697624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536604-G-A

135698391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537348-T-A

135699980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539628-C-G

135699980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539628-C-T

135700668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539933-T-C

135700677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539942-C-T

135700684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539954-G-A

135700684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539954-G-T

135700743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540034-A-T

135700860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540138-C-T

135700967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540251-C-T

135701057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540349-G-A

135701295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540564-G-A

135701361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540618-C-T

135701497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540697-A-G

135701550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540741-T-C

135702012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541890-A-G

135702180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542030-T-C

135702491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542296-G-A

135702502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542307-C-G

135702740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542802-A-G

135702816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542877-T-G

135702865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542909-T-A

135703099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543099-G-A

135703146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543147-A-G

135703225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543222-A-G

135703275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543259-A-G

135703346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543327-G-T

http://identifiers.org/hco/5/GRCh38#135703406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56543369-C-A

135703457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543431-G-A

135703883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543734-C-T

135703928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543782-C-G

135705464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544151-G-A

135705524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544224-A-G

135705718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544336-A-G

135705966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544588-C-G

http://identifiers.org/hco/5/GRCh38#135706178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56544731-A-C

http://identifiers.org/hco/5/GRCh38#135706271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56544839-A-C

135706279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544845-T-C

135706317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544878-C-T

135706370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56544917-G-C

135708880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545914-G-A

135708895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56545928-A-G

135709031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546064-G-A

135709067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56546099-A-G

135711506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548558-G-C

135711625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548723-A-T

135711854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548948-G-C

http://identifiers.org/hco/5/GRCh38#135711887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56548980-C-A

135711887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548980-C-T

135711918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549007-C-G

135711923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549012-T-C

135711923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549012-T-G

http://identifiers.org/hco/5/GRCh38#135711939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56549024-C-A

http://identifiers.org/hco/5/GRCh38#135711959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56549044-A-C

135711959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549044-A-G

135711982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549069-G-A

135712058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549135-T-C

135712060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549137-G-A

135712276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549346-G-T

135712372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549426-G-A

135712754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56549616-T-C

135712986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550361-A-G

135713099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550464-A-G

135713129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550468-C-T

135713191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550532-G-A

135713306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550638-G-A

135713429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550755-C-T

135713504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550836-C-G

135713949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551199-C-T

135714489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551744-G-A

135714489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551744-G-C

135714509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551763-C-T

http://identifiers.org/hco/5/GRCh38#135714581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56551820-C-A

135714622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551860-G-T

135714736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56551961-T-C

135714769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56551997-A-G

135714814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56552032-A-G

http://identifiers.org/hco/5/GRCh38#135714837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56552055-C-A

135714841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552096-G-T

135715077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552312-A-G

135715491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552731-C-T

135715652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552898-G-A

135715788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553033-A-G

135716080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553294-C-T

135716095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553309-G-A

135718183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56554604-A-G

135718186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56554607-G-C

135718204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554625-G-T

135718225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554646-C-T

135718242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554663-G-C

http://identifiers.org/hco/5/GRCh38#135718258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56554679-C-A

135719173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56557941-G-A

135719263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56558032-A-T

135719289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56558058-G-A

135719421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56558174-G-C

135719533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56558272-C-T

135719658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559018-A-G

135719693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559051-G-A

135719693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559051-G-T

135719899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559217-G-T

135720035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559310-G-T

135720290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559566-C-G

135720290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559566-C-T

135720438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559662-C-G

135720540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559758-C-T

135720661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559892-G-T

135720686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559915-C-G

135720783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560010-G-T

135721671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560305-C-G

135721671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560305-C-T

135721672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560306-G-A

135721672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560306-G-C

135721672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560306-G-T

135721786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560392-T-C

135721902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560516-T-A

135721978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560592-C-T

135722367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56560961-C-T

http://identifiers.org/hco/5/GRCh38#135722448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56561035-C-A

135722448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56561035-C-T

135722549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56561126-G-A

135722970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562132-G-A

135723246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562336-T-A

135723257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562347-A-G

135723413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562895-C-T

135723512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56562991-T-A

135723995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563416-T-C

135723997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56563418-T-C

http://identifiers.org/hco/5/GRCh38#135724002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56563420-A-C

135725289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566386-G-A

135725355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566438-G-C

135725646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566677-G-A

135725718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566737-T-A

135725923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566918-T-C

135725986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566989-C-T

135725992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56566995-C-G

135726021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567024-T-C

135726354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567670-T-C

135726446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567823-T-C

135726476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567852-C-T

135726585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567932-G-A

135726586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567933-G-C

135726652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567997-C-T

135726845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568125-G-A

135729137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569754-A-G

135729212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569820-G-T

135729557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570196-G-T

135729760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570369-T-C

135820623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573357-T-C

135820920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573636-G-C

135821185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573848-A-G

135821269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573949-G-A

135821474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574121-C-G

135821842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56574460-T-C

135821842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56574460-T-G

http://identifiers.org/hco/5/GRCh38#135821852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56574470-C-A

135821852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56574470-C-T

135821854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56574472-G-T

135821984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56574596-T-C

135822180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574771-G-A

135822180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574771-G-T

http://identifiers.org/hco/5/GRCh38#135822215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56574788-C-A

135822215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574788-C-T

http://identifiers.org/hco/5/GRCh38#135822263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56574814-C-A

http://identifiers.org/hco/5/GRCh38#135822275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56574826-C-A

135822275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574826-C-T

135822387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56574930-A-T

135822796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56575256-G-A

135822964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56575425-T-G

135822988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56575453-C-T

135823630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576141-A-G

135823795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576290-C-T

135824143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576595-G-A

135824166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576608-C-T

http://identifiers.org/hco/5/GRCh38#135824278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56576756-A-C

135824278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576756-A-G

135824304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576782-G-A

135824339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576808-G-T

135824378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576829-A-G

135824378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56576829-A-T

135824411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576862-G-A

135824411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576862-G-T

135824420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576871-C-T

135824423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576874-T-C

135824430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576881-G-A

135824430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576881-G-T

135824432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576883-A-G

135824447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576898-T-C

135824462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576913-G-T

135824509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56576960-G-T

135824589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577028-T-C

135824636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577114-A-T

http://identifiers.org/hco/5/GRCh38#135824754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56577241-C-A

135824754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577241-C-T

135824767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577254-A-G

135824849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577330-G-A

135824863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577344-C-T

135824957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577406-G-A

135824957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577406-G-T

135824968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577417-G-T

135824984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577432-A-G

135824986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577434-G-A

135824986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577434-G-T

135824993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56577441-G-T

http://identifiers.org/hco/5/GRCh38#135825005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56577453-C-A

135825224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577633-A-G

135825282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577687-A-G

135825443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577820-G-A

135825464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577841-C-T

135825616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577984-G-A

135825616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577984-G-T

135825635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56577991-T-C

http://identifiers.org/hco/5/GRCh38#135825679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578035-C-A

135825704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578060-G-A

http://identifiers.org/hco/5/GRCh38#135825706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578062-C-A

135825706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578062-C-T

135825784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578092-T-C

135825925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578229-G-A

135825925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578229-G-T

http://identifiers.org/hco/5/GRCh38#135825967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578270-C-A

135825979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578282-A-G

http://identifiers.org/hco/5/GRCh38#135825984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578287-C-A

135825984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578287-C-T

135826056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578364-G-A

135826089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578397-T-C

http://identifiers.org/hco/5/GRCh38#135826120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578436-C-A

135826120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578436-C-T

135826144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578459-A-G

135826144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578459-A-T

135826249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578562-T-C

135826364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56578673-G-T

http://identifiers.org/hco/5/GRCh38#135826370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56578679-C-A

135826387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578716-A-G

135826446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578772-T-C

135826453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56578777-A-T

135826508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56578832-A-G

135826560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56578878-T-C

135828746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56580341-C-T

135828916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56580516-T-C

135828925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56580525-G-A

135829607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56580913-G-A

135829759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581056-G-C

135829790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: 56581074-C-G

135829849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581127-G-T

135829990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581209-G-A

135829990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581209-G-T

135830010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: 56581232-G-A

135830124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: 56581331-C-T

135830545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581710-G-C

135830593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56581755-T-C

135831239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582036-C-T

135831452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582186-C-T

135831648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582365-T-C

135831827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582593-C-G

135832042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582844-G-A

135832101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56582910-G-C

135832199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56583007-C-T

135832372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56583107-G-T

http://identifiers.org/hco/5/GRCh38#135832530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56583235-C-A

http://identifiers.org/hco/5/GRCh38#135832644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56583305-C-A

135833279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56583840-T-C

135833453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56583991-C-G

135834509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56586004-G-C

135834509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56586004-G-T

http://identifiers.org/hco/5/GRCh38#135834519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586014-C-A

135834519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: 56586014-C-T

135834609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56586078-A-G

135834609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56586078-A-T

http://identifiers.org/hco/5/GRCh38#135834669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586138-A-C

135834669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586138-A-G

135834669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586138-A-T

http://identifiers.org/hco/5/GRCh38#135834734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586191-C-A

135834734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56586191-C-T

135834740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586197-C-G

135834740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586197-C-T

135834772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586222-G-A

135834772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586222-G-T

http://identifiers.org/hco/5/GRCh38#135834775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586225-C-A

http://identifiers.org/hco/5/GRCh38#135834777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586227-C-A

http://identifiers.org/hco/5/GRCh38#135834816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586267-C-A

135834816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586267-C-G

135834816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56586267-C-T

135834838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56586293-A-T

135834839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56586294-G-A

135834839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56586294-G-T

135834953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586419-T-C

135835009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586472-G-A

135835009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586472-G-C

135835009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586472-G-T

135835027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586492-T-C

135835028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586493-G-A

135835028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586493-G-T

135835062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56586524-T-C

135835062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56586524-T-G

http://identifiers.org/hco/5/GRCh38#135835071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56586544-C-A

135835121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56586591-A-G

135835138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56586608-G-T

135835198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56586670-G-T

135835307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56586782-T-C

135842106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590285-C-T

135842115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590294-T-C

135842265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590451-G-T

135842277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590463-G-A

135842277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590463-G-T

135842468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590654-G-T

http://identifiers.org/hco/5/GRCh38#135842469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56590655-C-A

135842469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590655-C-T

135842484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590669-C-G

135842554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590735-T-A

135842554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590735-T-C

135842557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590738-T-A

135842557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590738-T-C

135842557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590738-T-G

135842566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590755-G-T

http://identifiers.org/hco/5/GRCh38#135842572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56590761-C-A

135842572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590761-C-G

135842589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590775-A-G

135842601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590786-G-A

135842601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56590786-G-T

135842694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56591175-A-T

135842720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56591202-G-A

135842881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56591351-C-T

135843054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56591475-A-G

135843062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56591483-C-T

135848061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56594194-C-G

135848061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56594194-C-T

http://identifiers.org/hco/5/GRCh38#135848283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56594351-A-C

135848463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56594513-T-G

135848508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56594554-C-T

135848690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56595304-A-G

135848890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56595464-A-G

135849065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56595612-A-G

135849129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56595659-C-T

135849617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596072-G-T

135849687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596120-G-A

135849687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596120-G-T

135849837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596245-T-C

http://identifiers.org/hco/5/GRCh38#135849948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596352-C-A

135850021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596410-G-A

135850057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596444-A-G

135850188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596597-G-A

http://identifiers.org/hco/5/GRCh38#135850286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596691-C-A

135850286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596691-C-T

135850311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596715-G-T

http://identifiers.org/hco/5/GRCh38#135850314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596718-C-A

135850314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596718-C-G

135850314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596718-C-T

http://identifiers.org/hco/5/GRCh38#135850324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596728-C-A

135850324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596728-C-G

135850324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596728-C-T

http://identifiers.org/hco/5/GRCh38#135850333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596737-C-A

135850333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596737-C-T

135850344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596748-G-T

135850427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 56596813-T-C

http://identifiers.org/hco/5/GRCh38#135850571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56596959-C-A

135850571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596959-C-T

135850606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56596991-T-C

135850711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597091-C-T

135851315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597611-T-A

135851465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597763-G-A

135851572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597840-G-A

135851654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597893-G-A

135851702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597931-G-C

135851766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56597995-C-T

http://identifiers.org/hco/5/GRCh38#135851862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56598120-C-A

135851862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598120-C-T

135851887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598145-G-A

135851895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598153-G-A

135851895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598153-G-T

135852151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598414-C-T

135852164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598427-T-C

135852221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598520-A-G

135852249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598547-C-T

135852372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598620-G-A

135852523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56598791-C-T

135852652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56598923-G-A

135852700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56598971-C-T

135852811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56599082-G-A

135855992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56599264-C-T

http://identifiers.org/hco/5/GRCh38#135856109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56599358-C-A

135856350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56599494-G-A

135856536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56599679-G-T

135856614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56599753-G-A

135856780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56599826-G-A

135860396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56600047-T-C

135864530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56601187-G-T

135865211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56601761-G-A

135865233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56601799-T-A

135865233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56601799-T-C

135865250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56601816-C-G

http://identifiers.org/hco/5/GRCh38#135865329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56601896-A-C

135869513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609450-A-T

135869698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609633-A-G

135869747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609669-G-T

135869858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609746-A-G

135869937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609778-G-A

135870010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56609851-G-A

http://identifiers.org/hco/5/GRCh38#135870308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56610106-C-A

135870336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56610128-T-G

135870462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56610214-C-G

135870462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56610214-C-T

135870524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56610282-T-C

http://identifiers.org/hco/5/GRCh38#135870708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56610803-A-C

135871197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611056-G-A

135871197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611056-G-T

http://identifiers.org/hco/5/GRCh38#135871357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611213-C-A

http://identifiers.org/hco/5/GRCh38#135871358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611214-A-C

135871358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611214-A-G

135871376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611234-A-G

http://identifiers.org/hco/5/GRCh38#135871413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611268-C-A

http://identifiers.org/hco/5/GRCh38#135871422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611277-C-A

135871422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611277-C-T

135871485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56611340-C-T

http://identifiers.org/hco/5/GRCh38#135871486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611341-A-C

135871645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56611485-G-C

135871648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56611488-T-A

135871677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56611517-G-A

135871721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56611561-A-G

135871728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56611568-G-A

135871757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56611604-G-C

http://identifiers.org/hco/5/GRCh38#135871803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611655-C-A

135871803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56611655-C-T

135871870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56611732-C-G

135871870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56611732-C-T

135871929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611790-C-T

135871947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611808-C-T

http://identifiers.org/hco/5/GRCh38#135872019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611879-C-A

135872019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611879-C-T

135872050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611911-G-T

http://identifiers.org/hco/5/GRCh38#135872088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611936-C-A

135872088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611936-C-T

135872118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611946-A-G

135872118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611946-A-T

http://identifiers.org/hco/5/GRCh38#135872136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611951-C-A

http://identifiers.org/hco/5/GRCh38#135872173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611959-C-A

135872173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611959-C-T

http://identifiers.org/hco/5/GRCh38#135872175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56611961-C-A

135872175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611961-C-G

135872175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611961-C-T

135872176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611962-T-A

135872176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611962-T-C

135872176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611962-T-G

135872177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611963-G-A

135872177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611963-G-C

135872177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56611963-G-T

135872264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56612013-A-G

http://identifiers.org/hco/5/GRCh38#135872357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56612107-C-A

135872371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56612120-T-A

135872371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56612120-T-C

135873521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612360-C-T

135873594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612423-C-T

135873599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612428-C-T

135873812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612584-G-A

135873928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612671-A-G

135873928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612671-A-T

135873943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612686-G-A

135873988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612729-T-C

135873988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612729-T-G

http://identifiers.org/hco/5/GRCh38#135874113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56612860-C-A

135874113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56612860-C-T

135874138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56612885-A-G

135874223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56612963-G-T

135874226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 56612966-G-A

135874226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56612966-G-T

135877207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615676-C-T

135877235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615704-T-A

http://identifiers.org/hco/5/GRCh38#135877240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56615709-C-A

135877240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615709-C-G

135877240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615709-C-T

135877300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615753-T-A

http://identifiers.org/hco/5/GRCh38#135877460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56615884-C-A

135877471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615895-G-A

http://identifiers.org/hco/5/GRCh38#135877496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56615922-A-C

135877516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615940-G-T

135877814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616166-C-T

135877822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616174-G-A

135877823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616175-G-A

135877823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616175-G-T

135877886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616236-C-T

135877963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616308-G-A

135878047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616344-C-T

135878079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616365-G-A

135878192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616403-G-A

http://identifiers.org/hco/5/GRCh38#135878540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56616636-C-A

135878540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616636-C-T

135878696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616686-G-A

135878699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616689-T-C

135878907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616870-C-G

135878977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616917-C-T

135879146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617079-G-A

135879146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617079-G-T

135879324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617379-C-T

135879371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617444-G-A

http://identifiers.org/hco/5/GRCh38#135879520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56617723-C-A

135879557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617759-T-C

135879578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617780-C-T

135879603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617805-A-T

135879613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617815-T-A

135879613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617815-T-G

135879647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617830-T-A

135879792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617996-C-G

135879814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618003-T-A

135879841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618027-G-A

135879841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618027-G-C

135879935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618126-A-G

http://identifiers.org/hco/5/GRCh38#135880009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56618204-C-A

135880093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56618289-G-A

135880093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56618289-G-T

http://identifiers.org/hco/5/GRCh38#135880163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56618346-C-A

135880163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618346-C-T

http://identifiers.org/hco/5/GRCh38#135880211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56618384-C-A

135880220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618393-G-A

135880220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618393-G-T

135880227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618400-T-A

135880227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618400-T-C

http://identifiers.org/hco/5/GRCh38#135880254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56618423-A-C

135880254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618423-A-G

135880377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618533-A-G

135880386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618542-T-C

135880510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618663-A-G

http://identifiers.org/hco/5/GRCh38#135880698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56618791-A-C

135880729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56618830-C-T

135880752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56618849-C-T

135880920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619015-G-A

135880920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619015-G-T

http://identifiers.org/hco/5/GRCh38#135880946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56619044-C-A

135880946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619044-C-T

135880956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619054-G-A

135880956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619054-G-C

http://identifiers.org/hco/5/GRCh38#135880958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56619056-A-C

135880973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619068-G-A

135881026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619112-A-G

135881122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619131-T-A

135881246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619248-G-A

135881288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619300-A-G

135881437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619428-A-T

135881619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619622-A-T

135881727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619750-T-C

135881846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619838-T-A

135881893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619878-C-T

http://identifiers.org/hco/5/GRCh38#135881972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56619959-A-C

135881995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619984-C-T

135882089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620064-A-T

135882121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620096-C-G

135882121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620096-C-T

135882149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620124-G-A

135882428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620705-T-C

135882457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620735-G-T

135882487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620768-C-T

135882695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620999-C-T

135882791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56621092-G-T

135882872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56621173-C-T

135882874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 56621175-T-C

135882910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56621211-A-G

http://identifiers.org/hco/5/GRCh38#135882917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56621222-C-A

135882917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56621222-C-T

135882947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56621259-A-G

http://identifiers.org/hco/5/GRCh38#135882983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56621291-A-C

135882995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56621303-G-A

135882995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56621303-G-T

135883063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 56621382-G-T

135883070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56621389-C-G

135883070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56621389-C-T

135883072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56621391-C-T

135883095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56621409-T-C

135883106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56621420-C-T

135883143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621474-C-G

135883176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621505-A-G

135883183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621508-C-T

135883193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621518-T-C

135883271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621577-G-A

135883271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621577-G-T

http://identifiers.org/hco/5/GRCh38#135883274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56621580-C-A

135883283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621589-A-G

http://identifiers.org/hco/5/GRCh38#135883308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56621614-C-A

135883308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621614-C-T

135883437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621692-G-A

135883437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56621692-G-T

135883471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56621725-G-A

135883471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56621725-G-T

135883880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622085-C-G

135883880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622085-C-T

135883881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622086-G-A

135883895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622101-T-C

135883984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622168-T-C

135884032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622222-C-T

135884531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56622835-G-A

135884719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56623011-G-T

135884760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56623036-G-A

135887566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron_variant, undefined
orthologous variants: 56623358-G-T

http://identifiers.org/hco/5/GRCh38#135888004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56623591-C-A

135888005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56623592-T-C

135888006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: intron variant
orthologous variants: 56623593-G-A

135888030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: splice acceptor variant
orthologous variants: 56623619-A-G

135888030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: splice acceptor variant
orthologous variants: 56623619-A-T

135888078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 56623669-C-T

http://identifiers.org/hco/5/GRCh38#135888079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56623670-A-C

135888079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 56623670-A-G

135888098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56623689-G-T

http://identifiers.org/hco/5/GRCh38#135888118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56623706-C-A

135888174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56623751-G-T

http://identifiers.org/hco/5/GRCh38#135888181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56623758-C-A

135888202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 56623779-G-T

135888256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56623823-G-T

http://identifiers.org/hco/5/GRCh38#135888486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56623985-C-A

135888486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56623985-C-G

135888486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56623985-C-T

http://identifiers.org/hco/5/GRCh38#135888522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56624016-C-A

135888522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624016-C-G

135888522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624016-C-T

http://identifiers.org/hco/5/GRCh38#135888524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56624018-C-A

135888527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624021-G-A

135888527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624021-G-T

135888789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624321-A-G

135888789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624321-A-T

http://identifiers.org/hco/5/GRCh38#135888822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#56624362-C-A

135888822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30451
most severe consequence: 3 prime UTR variant
orthologous variants: 56624362-C-T