31514116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5 prime UTR variant
orthologous variants: 55813900-G-A

31514116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5 prime UTR variant
orthologous variants: 55813900-G-T

31514302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: 55814151-T-A

31514571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: 55814403-G-A

31514571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: 55814403-G-C

31514792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: -G-C

31515127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: -G-C

http://identifiers.org/hco/7/GRCh38#31515192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: -C-A

31515337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron variant
orthologous variants: -A-G

31518351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55821989-G-A

31518482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55822120-G-T

http://identifiers.org/hco/7/GRCh38#31518638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55822264-C-A

31518870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55822488-G-A

31518913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55822531-C-G

31519030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55822647-A-T

31524371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55824291-T-A

31524461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55824377-A-G

31524641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55824554-G-A

31525321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55825262-A-T

31525472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55825426-G-A

31526644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55828402-T-G

31527365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829096-C-G

http://identifiers.org/hco/7/GRCh38#31527410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55829140-C-A

31527410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829140-C-G

31527414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829144-C-T

31527480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829215-T-A

31529122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829552-T-C

31529294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829763-T-C

31529392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829869-G-T

31529401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829878-G-A

31529401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55829878-G-C

http://identifiers.org/hco/7/GRCh38#31529484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55829954-C-A

31529484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55829954-C-T

31529504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55829974-G-A

31529504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55829974-G-T

31529516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55829985-A-G

31529585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830055-T-C

http://identifiers.org/hco/7/GRCh38#31529589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55830059-C-A

31529589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830059-C-G

31529589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830059-C-T

31529652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830129-A-G

31529697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830168-T-A

31529733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830197-G-A

31529748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55830210-A-G

31529893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55830338-G-A

31530413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55830871-G-A

http://identifiers.org/hco/7/GRCh38#31530417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55830875-C-A

31530463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55830921-T-C

31530484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55830957-G-T

31530546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831056-A-G

31530729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831282-G-A

31530816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831374-A-G

http://identifiers.org/hco/7/GRCh38#31530826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55831384-A-C

31530862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831427-G-C

31530910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831456-C-T

31530919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831469-T-C

31531053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831523-C-G

31531085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831553-G-A

31531169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831765-G-A

31531219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55831815-A-G

31543989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840026-T-A

31544022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840047-C-T

31544398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840379-A-G

31544441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840417-A-G

31544441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840417-A-T

31544552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840614-T-G

31544556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840618-T-A

31544683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840767-G-A

31544711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840795-C-G

31544711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840795-C-T

31544854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841531-A-T

31544856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841533-T-C

31544896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841575-A-G

31544937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841620-C-T

31545074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841755-C-T

31545082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841763-G-A

31545213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841868-A-T

31545621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842264-C-G

31545631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842274-G-A

31546241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842885-G-T

31546288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842931-A-G

31546288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842931-A-T

31546358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55842981-G-A

31546501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55843061-A-G

31546506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55843066-G-C

31546522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55843082-C-T

http://identifiers.org/hco/7/GRCh38#31546831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55843392-A-C

31547041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55843602-G-A

31547155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55843698-C-T

31547767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55844178-A-T

31548443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55844799-G-T

31548489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55844862-C-T

31548540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55844913-G-A

31548614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55844976-G-C

31548743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845077-A-T

31548953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845433-A-G

31549026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845509-G-T

31549049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845531-A-G

31549109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845606-C-G

http://identifiers.org/hco/7/GRCh38#31549218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55845709-A-C

31549266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845756-A-G

31549304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845794-T-C

http://identifiers.org/hco/7/GRCh38#31549305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55845795-C-A

31549305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845795-C-G

31549425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 55846720-G-A

31549425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 55846720-G-C

31549449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55846744-A-G

31549477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55846767-A-G

http://identifiers.org/hco/7/GRCh38#31549481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55846771-A-C

http://identifiers.org/hco/7/GRCh38#31549491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55846781-A-C

31549630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846911-G-A

31549630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846911-G-T

31550046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847381-T-G

31550188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847511-G-A

31550188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847511-G-T

31550270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847576-C-T

31550308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847598-G-T

31550375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847661-C-G

http://identifiers.org/hco/7/GRCh38#31550522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55847817-C-A

31550522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847817-C-G

31550602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847896-A-G

31550631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55847924-G-A

31551102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55848331-T-G

31551223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55848449-A-G

31551294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55848508-T-A

http://identifiers.org/hco/7/GRCh38#31551711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55848873-C-A

31551806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55848972-T-C

31551833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55848998-G-T

http://identifiers.org/hco/7/GRCh38#31551863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55849026-C-A

31551921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849082-A-G

31551928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849089-C-T

http://identifiers.org/hco/7/GRCh38#31551952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55849114-C-A

31551959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849121-A-T

31552702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849189-T-A

31552812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849286-G-A

31552851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849325-G-T

31552871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849345-T-C

31552913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849386-G-A

31552913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849386-G-T

http://identifiers.org/hco/7/GRCh38#31552939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55849400-A-C

31553012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55849459-G-T

31553204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55849647-G-T

31553244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849687-T-G

31553260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849702-G-T

31553266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849708-G-A

31553266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849708-G-T

31553267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849709-G-A

31553267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849709-G-T

31553336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849772-T-A

31553336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849772-T-C

31553344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849780-G-A

http://identifiers.org/hco/7/GRCh38#31553444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55849848-C-A

31553444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55849848-C-G

31553686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55850513-G-T

31554083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55850898-T-C

http://identifiers.org/hco/7/GRCh38#31554264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55851079-C-A

31554264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851079-C-T

31554509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55851319-G-A

31554572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851402-C-T

31554583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851413-A-G

31554583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851413-A-T

31554602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851433-G-C

31554602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851433-G-T

31554692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851545-A-T

http://identifiers.org/hco/7/GRCh38#31554721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55851556-C-A

31554721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851556-C-T

31554733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851568-T-C

31554748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851573-C-T

31554753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851578-T-A

31554819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851638-A-G

31554845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851664-T-C

31554971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55851798-A-T

31555157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55851966-C-T

31555162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55851971-G-A

31555195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55852003-T-C

31555706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852495-G-T

31556042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853544-C-G

31556042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853544-C-T

31561527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854202-G-A

http://identifiers.org/hco/7/GRCh38#31561637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55854307-C-A

31561655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854325-G-A

31561755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854414-G-A

31561902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854521-C-T

31562144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854674-G-A

31562775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855432-C-T

31562978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855710-A-G

31563032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855744-C-T

31563073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855783-G-A

31563073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855783-G-C

http://identifiers.org/hco/7/GRCh38#31563075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55855785-C-A

31563075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855785-C-T

31563514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856192-G-T

31563759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856355-G-T

31563872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856447-G-A

31563943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856519-G-A

31564463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856992-A-G

31564692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857221-C-T

31564746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857269-G-A

31564815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857332-C-G

31564815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857332-C-T

31564961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857476-A-G

31565213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857698-C-T

31565218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857703-C-T

31565380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857861-C-T

31565393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857874-T-G

31565790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857969-C-G

31565980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858133-G-C

31565980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858133-G-T

http://identifiers.org/hco/7/GRCh38#31565984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55858137-A-C

31565984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858137-A-G

31566164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858313-T-C

31566232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858381-G-A

http://identifiers.org/hco/7/GRCh38#31566245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55858394-C-A

31566245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858394-C-G

31566480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858622-C-G

31566704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858871-C-T

31566783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858950-G-A

31566823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55858990-T-C

31566860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55859027-C-G

31567719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55859376-C-T

31568049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55859627-T-C

31568215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55859720-G-T

31568328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55859983-C-G

31568576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55860223-A-G

http://identifiers.org/hco/7/GRCh38#31568677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55860324-A-C

31568677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55860324-A-G

31569044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55860936-C-T

31569088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55860976-A-G

31569144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861059-G-T

31569160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861075-C-G

31569269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861240-C-T

http://identifiers.org/hco/7/GRCh38#31569312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55861269-C-A

31569509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861434-C-T

31569572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861505-G-A

31569724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861626-A-T

31569817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55861740-G-A

31569817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55861740-G-T

31569820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861743-G-A

31569820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861743-G-T

31569886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55861800-A-G

31570217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55862095-G-A

31570293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55862161-C-T

31571021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55862852-T-C

31571713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55863605-G-A

http://identifiers.org/hco/7/GRCh38#31571846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55863738-C-A

31572017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55863903-G-C

31572017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55863903-G-T

31572033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55863919-A-G

31572041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55863927-T-C

31572343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55864225-A-T

31572348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55864230-G-A

31572836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55864733-G-A

31574182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55865657-C-T

31574384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55865848-T-A

31574395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55865860-A-G

31574653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55866117-G-A

31574653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55866117-G-C

31574758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866221-G-A

31574763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866226-A-G

31574833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866305-G-A

31574833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866305-G-T

31574945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866408-G-A

31574945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866408-G-C

31575292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866691-A-G

31575399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866805-G-T

http://identifiers.org/hco/7/GRCh38#31575463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55866868-A-C

31575463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866868-A-G

31575541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866943-G-T

31575562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55866965-A-G

31575648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55867074-G-A

31575877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868042-G-A

31575977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868124-C-G

31575977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868124-C-T

31575980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868127-C-T

31576018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868156-A-G

http://identifiers.org/hco/7/GRCh38#31576562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55868647-C-A

31576663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868740-G-A

31576678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868755-C-T

31576767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55868850-C-T

31576904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873318-A-G

31576905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873319-C-G

31576905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873319-C-T

31576917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873327-T-C

31576936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873335-A-G

31576936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873335-A-T

31576942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873341-G-T

31577003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873402-A-G

31577453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873870-G-C

31577453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873870-G-T

31577480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55873947-T-C

31577556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874063-G-A

31577681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874188-C-T

31577717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874236-A-G

http://identifiers.org/hco/7/GRCh38#31577751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55874341-C-A

http://identifiers.org/hco/7/GRCh38#31577784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55874551-C-A

31577784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874551-C-G

31577784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874551-C-T

31577808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55874581-T-C

31577888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55874675-G-A

31577922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55874709-A-G

31577948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55874735-A-T

31578064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55874851-G-A

31578064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55874851-G-T

31578081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55874868-G-A

31578100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55874887-T-A

31578254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55875056-T-C

31578337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55875139-A-G

31578347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55875149-T-A

31578347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55875149-T-C

http://identifiers.org/hco/7/GRCh38#31578404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55875206-C-A

31578404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55875206-C-G

http://identifiers.org/hco/7/GRCh38#31578480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55875280-C-A

31578480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55875280-C-T

http://identifiers.org/hco/7/GRCh38#31578506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55875312-C-A

http://identifiers.org/hco/7/GRCh38#31578529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55875335-A-C

31578882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55876408-C-G

31581811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55877632-C-G

31582666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55877945-G-A

31582792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878078-A-T

31582974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878262-A-G

http://identifiers.org/hco/7/GRCh38#31583001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55878289-A-C

31583015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878299-G-C

31583015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878299-G-T

31583018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878302-T-G

http://identifiers.org/hco/7/GRCh38#31583037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55878321-C-A

31583037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878321-C-T

http://identifiers.org/hco/7/GRCh38#31583041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55878325-C-A

31583041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878325-C-G

http://identifiers.org/hco/7/GRCh38#31583047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55878331-A-C

31583047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878331-A-G

31583167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55878457-C-T

31583200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878490-T-C

31583206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878496-A-G

http://identifiers.org/hco/7/GRCh38#31583220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55878510-A-C

31583913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55878854-A-G

31584915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55886448-C-T

31584984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55886519-C-T

31585320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55886810-C-T

31585324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55886814-C-T

31585506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887011-A-G

http://identifiers.org/hco/7/GRCh38#31585677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55887183-C-A

31585799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887305-C-G

31588660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887701-T-A

31588685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887726-G-T

31588691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887732-A-G

31588829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55887868-G-T

http://identifiers.org/hco/7/GRCh38#31588936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55887975-A-C

31588996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55888049-G-A

31589033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55888086-G-A

31589291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55888449-A-G

http://identifiers.org/hco/7/GRCh38#31589530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55888686-C-A

31589688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55888831-A-T

31589793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55888939-G-A

31589877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889001-A-G

31589967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889073-G-C

31590008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889119-G-T

31590649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889657-T-C

31591034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889833-T-G

31591050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889849-G-T

31591087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55889880-G-A

31591381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55890146-C-T

31591561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55890301-G-A

31591707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55890443-T-C

31591869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55890715-A-G

http://identifiers.org/hco/7/GRCh38#31591895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55890741-A-C

31592129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55890956-C-T

31592317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55891113-T-A

31592853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

31595038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55892430-A-T

31595356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55892476-A-T

31595462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55892547-A-G

31595826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55893412-G-A

31596020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55893589-T-G

31596050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55893614-G-T

http://identifiers.org/hco/7/GRCh38#31596058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55893622-C-A

http://identifiers.org/hco/7/GRCh38#31601394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55896338-C-A

31601394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896338-C-T

31601395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896339-G-T

31601735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896659-A-G

31601766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55896704-T-G

31602051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897092-C-T

31602054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897095-C-T

31602144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897184-G-A

31602772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897818-G-A

31602820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897883-T-C

31602853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55897984-C-T

31603567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55898692-A-G

31603567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55898692-A-T

31603792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55898892-A-G

31603940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55899041-A-G

31604000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55899098-A-G

31604100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55899193-A-T

31604232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900224-C-T

31604428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900484-G-A

31604439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900495-T-C

31604459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900514-C-G

31604459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900514-C-T

31604677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55900780-T-C

31605387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901063-A-G

31605591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901261-A-G

31605656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901333-G-A

31605714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901390-G-A

31605742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901415-T-G

31605820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901487-A-G

31605837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901501-G-A

31605968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901624-G-T

31606002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901652-C-T

31606056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901703-A-G

31606065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901712-G-A

31606215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901841-C-G

31606350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55901982-G-A

31606550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903290-G-T

31606566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903307-C-T

31606570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903311-A-G

31606745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903482-T-C

31606748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903485-T-A

31606927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903709-C-T

31607086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903838-C-T

31607253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55903998-G-A

http://identifiers.org/hco/7/GRCh38#31613903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55917040-A-C

31613903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917040-A-G

31614110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917177-A-G

31614130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917196-C-G

31614162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917228-G-C

31614352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55917386-C-T

31614391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918167-T-C

31614450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918225-T-G

31614595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918354-C-G

31614694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918429-G-C

31614764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55918498-G-T

http://identifiers.org/hco/7/GRCh38#31617112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55919886-C-A

31617112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55919886-C-T

31617132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55919910-A-G

http://identifiers.org/hco/7/GRCh38#31617177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55919954-C-A

http://identifiers.org/hco/7/GRCh38#31617259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55920064-C-A

31617259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55920064-C-T

31617299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55920115-T-C

31617373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55920188-T-G

31617374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55920189-C-G

31617374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55920189-C-T

31625911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55921638-C-T

31626003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55921714-A-G

31626006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55921717-A-T

31626227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55921937-A-G

31626277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55921986-G-A

31626295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55922005-A-G

31626297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55922007-C-T

http://identifiers.org/hco/7/GRCh38#31626519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55922185-A-C

31626593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55922257-T-C

31627184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55922756-C-T

http://identifiers.org/hco/7/GRCh38#31627340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55922887-A-C

31627341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55922888-G-A

31627635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923176-G-A

31627635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923176-G-C

http://identifiers.org/hco/7/GRCh38#31627638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55923181-C-A

31627638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923181-C-T

31627713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923291-C-T

31627776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923354-T-C

31627927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923465-G-A

31627927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923465-G-C

31627959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923496-A-G

31628008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923539-A-G

31628416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55923905-T-G

http://identifiers.org/hco/7/GRCh38#31628817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55924139-A-C

31628817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924139-A-T

http://identifiers.org/hco/7/GRCh38#31628905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55924222-C-A

31628929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924246-A-T

31628930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924247-C-G

31629381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924672-C-T

31629415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924706-A-T

31629603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924872-G-A

31629639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55924905-G-A

31629856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55925081-A-G

31630036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55925239-T-C

31630119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55925320-G-T

31633373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927222-A-G

31633461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927308-C-T

http://identifiers.org/hco/7/GRCh38#31633570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55927411-A-C

31633627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927464-G-A

31633739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927564-C-T

31633837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927661-T-C

31633869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55927696-G-C

31634250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928040-G-C

31634381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928160-G-T

31634551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928261-C-T

31634556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928266-G-A

31634612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928323-A-G

31634819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928529-G-A

31634915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928641-A-G

31634995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928711-T-C

31635025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928739-T-C

31635171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55928864-T-C

31635352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55929034-A-G

31638067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55930150-A-T

31638224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55930294-T-C

31638321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932478-T-C

31638358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932515-A-G

31638457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932611-G-A

http://identifiers.org/hco/7/GRCh38#31638563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55932782-A-C

31638657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932887-T-C

31638701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55932928-T-A

31640118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55941995-T-C

31640127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942004-C-T

31640272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942102-A-G

31640447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942241-A-T

31640571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942361-G-A

31640928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942706-G-A

31640972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942747-G-A

31641148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55942887-T-G

31641285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943019-T-C

31641457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943304-G-A

31641567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943441-G-C

31641574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943472-C-T

31641706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943617-C-G

31641807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943714-A-G

31641838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943738-G-A

31642079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55943948-G-A

http://identifiers.org/hco/7/GRCh38#31642083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55943952-C-A

http://identifiers.org/hco/7/GRCh38#31642213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944082-C-A

31642213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944082-C-G

31642213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944082-C-T

31642297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944170-A-G

http://identifiers.org/hco/7/GRCh38#31642336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944196-A-C

31642336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944196-A-G

http://identifiers.org/hco/7/GRCh38#31642339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944199-C-A

31642339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944199-C-G

31642434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944350-G-C

31642459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944408-G-T

31642464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944413-G-A

http://identifiers.org/hco/7/GRCh38#31642561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944518-C-A

31642561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944518-C-G

31642561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944518-C-T

31642638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944566-T-C

31642638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55944566-T-G

http://identifiers.org/hco/7/GRCh38#31642646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944574-C-A

31642675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55944600-C-G

31642708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944633-T-C

31642723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944648-A-G

http://identifiers.org/hco/7/GRCh38#31642764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55944689-C-A

31642764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944689-C-G

31642780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944705-A-G

31642788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944713-A-G

31642820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944745-T-C

31642843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944768-T-A

31642846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944771-C-G

31642846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944771-C-T

31642909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944834-G-A

31642909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55944834-G-T

31643115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55944998-G-A

31643159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945048-C-G

31643159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 55945048-C-T

31643169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945058-C-G

31643169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945058-C-T

31643186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945075-C-G

http://identifiers.org/hco/7/GRCh38#31643217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55945106-C-A

31643217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945106-C-T

31643254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945143-C-G

31643254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55945143-C-T

31643332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55945221-T-A

31643475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945298-C-G

http://identifiers.org/hco/7/GRCh38#31643702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55945543-C-A

31643708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945549-A-G

31643750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945591-C-T

http://identifiers.org/hco/7/GRCh38#31643764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#55945605-C-A

31643764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55945605-C-T

31643772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945613-T-C

31643823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55945664-A-T

http://identifiers.org/hco/7/GRCh38#31643985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55945824-C-A

31643985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55945824-C-T

http://identifiers.org/hco/7/GRCh38#31644006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55945849-C-A

31644006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55945849-C-T

31644088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55945928-G-A

31644142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55945981-C-T

31644699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946546-T-G

31644793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946638-G-A

31644940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946770-A-G

31644941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946771-T-G

31644945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946775-G-A

31645003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946837-C-T

31645105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55946937-T-C

31645533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947263-G-C

31645573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947315-G-T

31645586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947350-C-T

31645768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947514-T-C

31645828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947578-G-A

31645828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947578-G-C

http://identifiers.org/hco/7/GRCh38#31645895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55947644-C-A

31645990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947735-G-A

31646046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55947786-G-A

31646654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55948404-A-G

31646690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55948440-G-C

31647003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949059-T-C

31647047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949103-C-T

http://identifiers.org/hco/7/GRCh38#31647087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55949148-C-A

31647087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949148-C-T

31647195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949235-A-G

31647343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949380-A-G

31647347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949384-G-A

31648089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949728-T-C

31648259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949888-A-G

31648264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55949893-T-C

http://identifiers.org/hco/7/GRCh38#31648616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55950246-C-A

31648768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55950367-A-G

31648795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55950394-A-G

31649960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55950806-G-A

31650108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55951085-C-T

31650288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55951803-A-G

31650413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55951913-T-C

31650607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952059-T-C

31650628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952081-A-T

31650690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952143-T-C

http://identifiers.org/hco/7/GRCh38#31650849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55952298-C-A

31650935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952378-A-T

http://identifiers.org/hco/7/GRCh38#31651078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55952519-C-A

31651190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55952621-C-T

31651252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55952683-C-T

31651380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952816-G-A

31651380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952816-G-C

31651380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952816-G-T

31651385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952821-G-A

31651385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952821-G-C

31651385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55952821-G-T

31651578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953024-A-T

31651584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953030-C-T

31651675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953177-A-G

31651793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953264-T-A

31651793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953264-T-G

http://identifiers.org/hco/7/GRCh38#31651891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55953283-C-A

31651905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953297-T-C

31651907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953299-A-T

http://identifiers.org/hco/7/GRCh38#31651932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55953321-C-A

31651932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55953321-C-T

31651962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55953351-C-G

31651962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55953351-C-T

31651966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55953355-A-T

31652060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953452-A-G

31652060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953452-A-T

31652064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953456-G-A

31652064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953456-G-T

31652077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953486-A-G

31652114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55953526-G-A

31652114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55953526-G-T

31652128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55953539-T-C

31652246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953629-A-T

31652323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953697-A-G

http://identifiers.org/hco/7/GRCh38#31652378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55953751-C-A

31652378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953751-C-G

31652378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953751-C-T

http://identifiers.org/hco/7/GRCh38#31652408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55953781-C-A

31652415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953788-A-G

http://identifiers.org/hco/7/GRCh38#31652419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55953792-A-C

31652430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953802-T-A

31652434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953807-A-T

31652467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953840-G-T

31652468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953841-G-A

31652468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55953841-G-T

31652500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55955130-C-T

31652748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55955375-A-G

31652774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55955401-C-T

31653039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55955580-G-A

31653050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55955590-G-A

31654206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55955928-A-G

31654332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55956048-C-G

31654332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55956048-C-T

31654356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55956065-G-A

31654376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55956086-C-T

http://identifiers.org/hco/7/GRCh38#31654458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55956167-C-A

31655641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55957578-G-A

31655641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55957578-G-T

31655732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55957667-C-T

31655975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55957857-T-C

http://identifiers.org/hco/7/GRCh38#31656369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55958104-A-C

31656459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55958193-T-G

31656467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55958198-A-G

http://identifiers.org/hco/7/GRCh38#31656519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55958252-C-A

31656519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958252-C-G

http://identifiers.org/hco/7/GRCh38#31656539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55958274-C-A

31656563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958298-A-G

31656575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958310-T-C

31656718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958432-G-A

31656747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55958461-T-G

http://identifiers.org/hco/7/GRCh38#31657169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55959152-C-A

http://identifiers.org/hco/7/GRCh38#31657179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55959162-C-A

31657179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27363
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55959162-C-T