http://identifiers.org/hco/16/GRCh38#18374587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806642-C-A

18374587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806642-C-T

18374590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806639-G-C

18374590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806639-G-T

18374617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806612-G-A

18374617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806612-G-T

18374762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-A

18374762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-C

18375065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24806155-G-A

18375065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24806155-G-C

18375065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24806155-G-T

18376620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805654-A-G

18376620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805654-A-T

18376854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24805442-C-T

18377152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24805147-G-T

18377195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805097-G-A

18377196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805096-C-T

http://identifiers.org/hco/16/GRCh38#18377247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805049-C-A

18377247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805049-C-G

18377247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805049-C-T

18377374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804922-T-G

18377535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-T-C

18377550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804757-T-C

18377550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804757-T-G

18377652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804655-G-A

18377652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804655-G-T

18377655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24804652-G-T

18379127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800766-G-A

18379143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-C-G

18379143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-C-T

18379357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 24800528-A-T

18379394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800487-T-C

18379521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24800369-C-T

18379542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24800348-G-A

18379644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24800246-T-C

18379737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-G-A

18379737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-G-C

18379737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-G-T

18379849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-G-A

18379849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-G-T

18380858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-G-A

18380858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-G-C

18381028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24798888-G-A

18381728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798079-T-G

18381801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798003-A-G

18381805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797999-T-C

18381997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797818-G-A

http://identifiers.org/hco/16/GRCh38#18382198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797669-A-C

18382264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797633-T-C

18382587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 24797349-T-A

18382587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 24797349-T-C

18382597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-G-C

18382597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797338-G-T

18382614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797321-T-C

18382660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-A

18382660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-T

18382757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797176-G-T

18382821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797112-G-A

18382821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24797112-G-T

18383056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24796904-G-T

18383259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796692-G-A

18383259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796692-G-T

18383260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796691-A-G

http://identifiers.org/hco/16/GRCh38#18383379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796621-C-A

18383379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24796621-C-T

http://identifiers.org/hco/16/GRCh38#18383742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796319-C-A

18383742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796319-C-T

18383753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796310-C-T

18383789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796282-G-A

18383789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796282-G-C

18383789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796282-G-T

18383842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796240-C-T

http://identifiers.org/hco/16/GRCh38#18383865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796217-C-A

18383865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796217-C-T

18383883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796200-G-A

http://identifiers.org/hco/16/GRCh38#18383963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796137-A-C

18383963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796137-A-G

18383997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796126-C-G

18384004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796119-C-G

18384004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796119-C-T

18384025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796091-C-G

18384058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796053-G-A

18384058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796053-G-T

18384513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24795490-A-G

18385087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794941-G-A

18385087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794941-G-T

18385189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794839-G-A

18385189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794839-G-C

18385189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794839-G-T

http://identifiers.org/hco/16/GRCh38#18385460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24794568-C-A

18385460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794568-C-T

18385461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794567-G-A

18385461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794567-G-T

18385570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794458-A-G

18385573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794455-G-A

18385573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794455-G-T

18385823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24794204-C-T

18386143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793884-A-G

18386143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793884-A-T

http://identifiers.org/hco/16/GRCh38#18386181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793846-C-A

18386181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793846-C-T

http://identifiers.org/hco/16/GRCh38#18386220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793810-C-A

http://identifiers.org/hco/16/GRCh38#18386302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793728-C-A

18386490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793540-C-G

18386490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793540-C-T

18386551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793479-A-G

18386613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793417-C-T

http://identifiers.org/hco/16/GRCh38#18386666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793364-C-A

18386666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793364-C-T

18386700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793330-A-G

18386722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793305-A-G

18386722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793305-A-T

18386757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793267-A-G

18386808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793210-C-G

http://identifiers.org/hco/16/GRCh38#18386809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24793209-C-A

18386809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793209-C-T

18386924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793094-G-A

18386962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793057-C-G

18387003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793016-G-A

18387003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793016-G-T

18387009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793010-C-G

18387009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24793010-C-T

http://identifiers.org/hco/16/GRCh38#18387211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24792808-C-A

18387211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24792808-C-T

18387295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24792724-A-G

18387634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24792385-C-T

18387672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24792347-A-T

18387830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24792189-C-T

18388126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24791893-G-A

18388126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24791893-G-C

18388729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791222-G-A

18388884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24791089-T-A

18388884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24791089-T-C

18388936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24791037-T-A

18388936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24791037-T-C

18388969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24791004-T-C

18389033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790940-G-A

18389043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790933-G-A

18389043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790933-G-C

18389095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-G-A

18389095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-G-T

18389102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-A

18389102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-C

18389102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-T

18389108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790908-G-A

18389108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790908-G-C

18389108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790908-G-T

18389109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790907-G-A

18389109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790907-G-T

18389119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790897-A-G

http://identifiers.org/hco/16/GRCh38#18389120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790896-C-A

18389120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790896-C-G

18389120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790896-C-T

18389126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790890-T-A

18389126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790890-T-C

18389126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790890-T-G

18389139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-T-A

18389139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-T-C

18389139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-T-G

18389280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790763-G-T

18389500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24790527-A-G

18389848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790148-G-A

18390041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789867-A-T

18390228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789660-C-T

18390452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789467-G-A

http://identifiers.org/hco/16/GRCh38#18390491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24789429-C-A

18390491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789429-C-T

18390965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-A-G

18390965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-A-T

18391090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24788731-G-A

18391090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24788731-G-T

18391135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24788686-C-T

18392325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787501-T-C

18392336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787490-G-A

18392794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787133-G-A

18392794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787133-G-T

18393026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786810-G-T

18393238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786554-T-C

18393238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786554-T-G

18393244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786548-G-C

18393244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786548-G-T

18393245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786547-T-C

18393286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786490-C-T

18393291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786485-G-A

18393291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786485-G-T

18393515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24786214-G-A

18393515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24786214-G-T

http://identifiers.org/hco/16/GRCh38#18393569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786160-C-A

18393569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24786160-C-T

http://identifiers.org/hco/16/GRCh38#18393586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786146-A-C

18393586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24786146-A-G

18393586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24786146-A-T

http://identifiers.org/hco/16/GRCh38#18393774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24785944-C-A

18393866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785138-A-G

18393890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785113-C-G

18393890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785113-C-T

http://identifiers.org/hco/16/GRCh38#18393995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24785020-C-A

18393995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785020-C-T

18394002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-A

18394002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-C

18394002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-G-T

18394007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785006-C-T

http://identifiers.org/hco/16/GRCh38#18394016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784996-A-C

http://identifiers.org/hco/16/GRCh38#18394035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784974-A-C

18394035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-A-G

18394035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-A-T

http://identifiers.org/hco/16/GRCh38#18394149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784862-C-A

18394149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784862-C-G

18394149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784862-C-T

18394337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784685-T-C

18394464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784561-C-T

18394520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-T-A

18394520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-T-C

http://identifiers.org/hco/16/GRCh38#18394548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784477-C-A

18394548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784477-C-G

18394548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784477-C-T

18394760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784265-G-T

http://identifiers.org/hco/16/GRCh38#18394769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784256-A-C

18394934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24784091-A-G

http://identifiers.org/hco/16/GRCh38#18395086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783935-C-A

http://identifiers.org/hco/16/GRCh38#18395097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783882-A-C

18395097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-A-G

18395887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24783192-G-A

18395887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24783192-G-T

18395919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: non coding transcript exon variant
orthologous variants: 24783160-C-T

18395963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24783116-G-A

18395963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24783116-G-T

18395984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783099-G-A

18395984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783099-G-T

18395985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783098-G-A

18395999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783084-T-C

18400624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770375-G-A

http://identifiers.org/hco/16/GRCh38#18400730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24770301-C-A

http://identifiers.org/hco/16/GRCh38#18401132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769977-C-A

18401132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769977-C-G

18401132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769977-C-T

http://identifiers.org/hco/16/GRCh38#18401135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769974-A-C

18401346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769792-G-A

18401346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769792-G-C

http://identifiers.org/hco/16/GRCh38#18401361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769775-C-A

18401361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769775-C-T

18401862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24769180-C-G

18401862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24769180-C-T