60916977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97517148-A-G

60916983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97517157-C-T

60917088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97517239-A-G

60917949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518016-G-A

60918074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518139-C-T

60918110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518174-G-A

60918124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518189-G-A

60918188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518357-G-A

60918213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518390-T-C

60918241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518480-C-G

http://identifiers.org/hco/1/GRCh38#60918253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97518530-A-C

60918253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518530-A-G

60918269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97518546-C-G

60918866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97519111-C-T

60918931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97519174-A-G

http://identifiers.org/hco/1/GRCh38#60919168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97519423-C-A

60919334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97519579-T-C

60920642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97520381-C-G

60921113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97520817-G-A

60921113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97520817-G-C

60921136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97520837-G-A

60921298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97521191-C-G

60921875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97521743-T-C

60922094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97521952-G-A

60922134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97521984-A-T

60922170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522006-G-A

60922239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522062-G-A

60922246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522069-T-G

60922266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522076-C-T

60922623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522435-G-A

60922660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522471-G-A

60922660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97522471-G-T

60923093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97523164-T-C

60923094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97523165-G-T

http://identifiers.org/hco/1/GRCh38#60923175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97523301-C-A

60923636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97523701-C-T

60923861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97523956-C-T

60923923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97524020-G-A

http://identifiers.org/hco/1/GRCh38#60923953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97524087-A-C

60924613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97524891-A-G

http://identifiers.org/hco/1/GRCh38#60924782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97525043-C-A

60924816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525076-A-T

60924913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525110-G-A

60925393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525525-C-T

60925398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525530-C-T

60925593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525698-G-A

60925593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525698-G-T

60925742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97525839-T-C

http://identifiers.org/hco/1/GRCh38#60925814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97525914-A-C

60926258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97526363-C-T

60926297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97526401-T-A

60927160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97526992-A-G

60927166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97526998-A-G

60927283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527092-C-T

60927477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527379-G-A

http://identifiers.org/hco/1/GRCh38#60927523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97527424-A-C

60927523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527424-A-G

60927646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527559-C-T

60927695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527602-A-G

60927704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527611-G-A

60927704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527611-G-T

60927718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97527625-C-T

60928214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528157-A-G

60928291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528235-A-T

60928515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528280-A-G

60930375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528772-T-C

60930389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528784-G-A

60930397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528793-A-G

http://identifiers.org/hco/1/GRCh38#60930440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97528832-A-C

60930440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528832-A-G

60930502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528896-G-A

60930507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97528901-C-G

http://identifiers.org/hco/1/GRCh38#60930533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97528927-C-A

http://identifiers.org/hco/1/GRCh38#60931092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97530132-A-C

http://identifiers.org/hco/1/GRCh38#60931123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97530162-C-A

60931594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97531385-G-A

60931682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97531468-A-G

60931715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97531501-C-T

60931774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97531556-T-C

60933159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533391-G-A

http://identifiers.org/hco/1/GRCh38#60933303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97533534-C-A

60933386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533619-G-A

60933419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533652-C-T

60933500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533704-C-T

60933663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533857-C-G

60933663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97533857-C-T

60933892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97534712-C-T

60933960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97534861-T-A

60934129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535028-C-G

60934152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535051-A-G

60934252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535153-C-G

60934375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535334-G-C

60934482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535445-T-C

60934512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535472-G-A

60934526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535486-C-T

60934880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97535847-A-G

60935286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97536261-G-T

60935447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97536434-G-A

60935464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97536451-T-A

60935515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97536502-C-T

60935720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97536649-T-G

http://identifiers.org/hco/1/GRCh38#60936069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97537017-C-A

60936494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97537431-A-G

60936502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97537439-G-A

http://identifiers.org/hco/1/GRCh38#60936621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97537501-C-A

60937665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97538543-A-G

60937715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97538581-G-T

60937903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97538764-G-A

60938063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97538888-A-G

60938085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97538909-A-T

60938536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97539227-T-A

http://identifiers.org/hco/1/GRCh38#60938756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97539445-C-A

60939037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97539764-T-C

60939152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97539884-T-C

60939239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97539977-G-T

60939383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540134-C-T

http://identifiers.org/hco/1/GRCh38#60939729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97540443-A-C

60939847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540600-A-G

60939850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540603-A-T

60940012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540748-A-G

60940029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540765-G-A

http://identifiers.org/hco/1/GRCh38#60940103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97540832-C-A

60940105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97540834-T-C

60943689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97541609-C-G

60943809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97541734-C-T

60944327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97542002-G-A

60944642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97542262-C-T

60945845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543028-A-G

60945845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543028-A-T

60945943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543127-T-C

60946048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543229-G-C

60946432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543543-G-T

60946516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543620-A-T

60946911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97543966-G-A

60947107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97544153-G-A

60947166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97544225-G-A

60947893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97544953-T-G

60948678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545198-C-T

60948714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545225-A-G

60948800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545315-A-T

60948820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545335-T-C

60948844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545346-G-A

60948844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545346-G-T

60948973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97545458-C-G

http://identifiers.org/hco/1/GRCh38#60949415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97545847-C-A

60949653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546056-G-A

60949854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546379-C-T

60949903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546425-G-A

60949965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546483-G-A

60950022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546544-A-G

60950257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546729-G-A

60950503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97546976-G-A

60950578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547039-A-G

60950582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547043-G-A

60950593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547054-C-T

60950733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547195-A-G

60950940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547380-G-A

60950940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97547380-G-T

http://identifiers.org/hco/1/GRCh38#60951165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97547596-C-A

60952078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549227-C-T

60952179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549329-T-C

60952266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549417-A-G

60952320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549460-T-C

60952401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549475-A-G

60952407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549481-G-T

http://identifiers.org/hco/1/GRCh38#60952419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97549492-C-A

60952475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549538-T-C

http://identifiers.org/hco/1/GRCh38#60952482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97549545-C-A

60952482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549545-C-T

60952495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549563-G-T

60952506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549592-C-T

http://identifiers.org/hco/1/GRCh38#60952551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97549638-C-A

60952551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549638-C-T

60952556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549643-G-A

60952556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549643-G-T

60952584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549665-G-A

60952584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549665-G-C

60952603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549684-T-C

60952670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549751-G-T

http://identifiers.org/hco/1/GRCh38#60952800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97549881-C-A

60952800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549881-C-T

60952801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97549882-G-A

60953132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550213-C-T

60953471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550538-G-A

60953471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550538-G-C

60953546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550613-G-A

60953546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550613-G-C

60953546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550613-G-T

60953775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550815-T-C

60953848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97550880-A-G

60953968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551026-G-A

60954090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551153-A-G

60954292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551311-A-G

http://identifiers.org/hco/1/GRCh38#60954397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97551405-C-A

60954397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551405-C-T

http://identifiers.org/hco/1/GRCh38#60954427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97551435-C-A

60954427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551435-C-G

60954427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551435-C-T

60954535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551520-C-T

60954667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551896-G-A

60954730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97551960-T-A

60954894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552078-T-C

60954937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552113-C-G

60955072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552231-G-T

60955178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552302-G-A

60955241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552361-A-G

60955917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97552989-C-G

60956016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553083-T-C

60956155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553208-C-T

60956681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553717-G-A

60956801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553834-T-C

60956827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553858-G-A

60956889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553920-A-G

60956904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553935-C-T

60956913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553949-C-T

60956918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553954-G-C

60956918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97553954-G-T

60956984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554017-A-G

60957101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554097-T-A

60957101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554097-T-C

60957373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554327-T-C

60957449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554408-T-G

60957729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554699-T-A

60957729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554699-T-G

60957795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554753-T-G

60957803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554761-C-G

60957804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554762-C-T

60957805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554763-C-T

http://identifiers.org/hco/1/GRCh38#60957915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97554854-C-A

60957915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554854-C-T

60957941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97554867-G-A

60958421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555336-G-A

60958421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555336-G-T

60958472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555383-T-C

60958613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555510-T-A

60958632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555529-A-G

60958674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97555568-G-A

http://identifiers.org/hco/1/GRCh38#60958754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97555648-C-A

http://identifiers.org/hco/1/GRCh38#60958837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97555720-A-C

60959039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556205-C-T

http://identifiers.org/hco/1/GRCh38#60959040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97556206-A-C

60959210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556376-G-A

60959224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556388-C-T

60959408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556577-G-A

60959408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556577-G-C

60959414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556583-C-T

60959461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556616-G-C

60959502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97556656-C-T

60959618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97557220-G-A

60959779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97557394-A-T

60959907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97557519-G-A

60960094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97557768-A-T

60960394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97558043-G-C

60960413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97558062-G-A

60960820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97558688-T-C

60961157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559031-C-T

60961271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559136-G-A

60961298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559163-T-C

60961315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559180-G-A

60961390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559251-A-T

60961428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559289-C-T

60961433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559294-T-C

60962115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559648-C-T

60962148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97559680-A-G

60963206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560349-C-T

60963257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560392-A-G

60963289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560424-G-T

60963374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560502-C-T

60963527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560631-A-G

60963681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560793-G-A

60963731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560842-A-G

60963731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560842-A-T

60963770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560880-G-T

60963874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97560983-G-A

60963930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561033-C-T

60964035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561134-C-T

60964143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561311-C-T

60964269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561438-A-G

60967430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561597-T-C

60967522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561685-C-G

60967595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561767-T-G

60967703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561870-G-T

60967717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97561884-G-A

http://identifiers.org/hco/1/GRCh38#60968014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97562134-C-A

60968060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562191-G-A

60968145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562278-C-T

60968467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562529-C-T

60968514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562580-G-T

60968561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562601-G-C

60968672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562705-A-G

60968672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97562705-A-T

60969184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563170-A-G

60969228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563211-C-T

60969277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563531-C-T

60969419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563667-T-C

60969537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563783-G-A

60969537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97563783-G-C

http://identifiers.org/hco/1/GRCh38#60969816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564018-A-C

http://identifiers.org/hco/1/GRCh38#60969855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564056-C-A

60969855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564056-C-T

60969951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564157-C-T

60969952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564158-G-A

60969952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564158-G-T

http://identifiers.org/hco/1/GRCh38#60969959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564165-C-A

60969968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564174-A-G

60969996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564200-T-C

60970057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564252-C-T

http://identifiers.org/hco/1/GRCh38#60970066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564260-C-A

60970066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564260-C-T

60970078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564272-T-A

60970078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564272-T-C

60970107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564302-G-T

60970109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564304-G-A

60970109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564304-G-T

60970143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564345-C-T

60970223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564426-G-A

60970434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564635-G-T

60970438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564639-A-G

60970475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564711-G-T

60970481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564717-C-G

60970481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564717-C-T

60970572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564782-T-C

http://identifiers.org/hco/1/GRCh38#60970605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564824-C-A

60970610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564829-T-C

http://identifiers.org/hco/1/GRCh38#60970673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97564887-C-A

60970673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97564887-C-T

60971090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565239-G-A

60971094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565243-G-T

60971104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565253-C-T

60971132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565266-T-A

60971195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565329-C-T

60971211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565346-G-A

http://identifiers.org/hco/1/GRCh38#60971248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97565382-C-A

60971297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565430-A-G

60971745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97565998-T-C

60972053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566345-A-T

60972095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566386-T-C

60972173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566465-C-T

60972201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566493-G-A

60972381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566672-C-T

60972791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97566999-C-T

60972797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567005-G-A

60972797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567005-G-C

60972800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567008-T-C

60972813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567021-T-C

60973164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567363-T-G

60973398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567569-C-T

60973417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567587-A-G

60973520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567684-A-G

60973620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567755-C-G

60973620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567755-C-T

60973689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567824-A-G

60973752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567885-A-G

60973775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567908-C-T

60973870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97567971-C-T

60973909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568005-T-C

60973930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568026-C-T

60974110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568184-C-T

60974251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568306-T-G

60974319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568363-C-G

60974994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97568971-A-G

60975299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569239-G-C

60975367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569303-A-G

60975380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569316-T-G

60975484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569401-C-G

60975484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569401-C-T

60975582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569520-C-T

http://identifiers.org/hco/1/GRCh38#60975708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97569623-A-C

60975731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569643-G-C

60975762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569665-A-G

60975791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569690-G-C

http://identifiers.org/hco/1/GRCh38#60975847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97569746-C-A

http://identifiers.org/hco/1/GRCh38#60975910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97569801-A-C

60975910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569801-A-G

http://identifiers.org/hco/1/GRCh38#60975921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97569812-A-C

60975921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569812-A-G

60975985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97569873-T-A

60976798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97570586-T-G

60976948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97570740-T-A

60977230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97570982-G-A

60977358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571110-A-G

60977434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571187-G-T

http://identifiers.org/hco/1/GRCh38#60977516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97571268-A-C

60977542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571280-G-A

60977695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571433-G-A

60977979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571574-A-G

60978048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571648-G-A

60978208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571792-A-G

http://identifiers.org/hco/1/GRCh38#60978366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97571964-C-A

60978366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571964-C-G

60978366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97571964-C-T

60978701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97572618-T-A

60978854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97572749-T-C

60978961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97572858-C-T

60980683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97573805-A-G

60980719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97573839-T-C

60980807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97573916-G-A

60980817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97573926-C-G

60980817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97573926-C-T

60980932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97574049-T-C

60980960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97574083-G-C

60981429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97574530-T-C

http://identifiers.org/hco/1/GRCh38#60981615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97575858-C-A

60981775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97576014-A-G

http://identifiers.org/hco/1/GRCh38#60981779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97576018-C-A

60981789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97576028-A-G

60981977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97576213-T-G

60982601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97576908-A-G

60982759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577078-G-A

60982759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577078-G-T

60982944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577256-T-C

60982952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577264-C-G

http://identifiers.org/hco/1/GRCh38#60982990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97577309-A-C

60983099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577424-A-G

60983099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577424-A-T

60983260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577584-G-C

60983260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97577584-G-T

60984202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97578433-C-T

60984715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97578834-G-A

60984941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97578975-T-C

http://identifiers.org/hco/1/GRCh38#60985019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97579031-C-A

60985264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97579240-G-A

60985651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97579631-A-G

60985742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97579770-C-T

60987101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97580563-T-C

http://identifiers.org/hco/1/GRCh38#60987172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97580633-A-C

60987296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97580757-C-T

60987811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97581274-C-T

60987938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97581396-T-A

60987946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97581404-A-G

60988568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97581928-C-G

60988829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97582167-A-G

60988903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97582226-G-A

60989152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97582466-A-G

http://identifiers.org/hco/1/GRCh38#60989499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97583251-A-C

60989694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97583426-T-C

60990199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97583857-C-T

60990396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584032-G-C

60990761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584394-G-A

60990761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584394-G-C

60990780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584413-C-T

60990786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584419-G-A

60990846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584482-A-G

60990885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584521-C-T

60990948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584583-G-A

60990948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584583-G-T

http://identifiers.org/hco/1/GRCh38#60990994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97584629-C-A

60990994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584629-C-T

60991109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584721-T-C

60991125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97584743-G-C

60991521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585350-C-T

60991672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585497-C-G

60991739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585564-A-G

60991860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585647-G-A

60992119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585926-G-T

60992169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97585948-T-C

http://identifiers.org/hco/1/GRCh38#60992242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97586008-A-C

http://identifiers.org/hco/1/GRCh38#60992440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97586196-A-C

http://identifiers.org/hco/1/GRCh38#60992472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97586225-C-A

60992540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586290-G-C

60992545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586295-G-A

60992631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586364-A-G

60992701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586419-A-G

60992749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586467-A-G

60992808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586527-G-A

60992901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586609-G-A

60992984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586690-G-A

60993190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97586893-G-C

60993372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587030-C-G

60993372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587030-C-T

60993547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587183-G-A

60993592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587228-G-A

60993592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587228-G-C

60993796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587392-C-T

60993868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587465-C-G

60994140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587705-G-A

60994207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587769-G-A

60994207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97587769-G-T

http://identifiers.org/hco/1/GRCh38#60994218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97587780-A-C

60994520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588066-C-T

60994595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588124-C-G

60994604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588132-C-T

60994884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588769-T-A

60994885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588770-C-G

60994955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588855-T-C

http://identifiers.org/hco/1/GRCh38#60995071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97588940-C-A

60995071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97588940-C-T

60995198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97589066-G-A

60995349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97589205-G-A

60995483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97589776-C-T

60995744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97589973-G-C

http://identifiers.org/hco/1/GRCh38#60995845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97590072-C-A

http://identifiers.org/hco/1/GRCh38#60995883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97590107-C-A

60995926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590149-T-G

60995930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590153-G-A

60995930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590153-G-T

60995951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590174-C-T

60996310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590218-A-T

http://identifiers.org/hco/1/GRCh38#60996335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97590243-C-A

60996353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590261-C-T

60996385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590293-G-A

60996397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590305-A-G

60996598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590472-T-A

60996676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590549-G-T

60996884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590595-T-G

http://identifiers.org/hco/1/GRCh38#60996914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97590633-A-C

60997069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590743-G-A

60997274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590923-G-A

60997289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590938-C-T

60997339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97590981-A-G

60997415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591049-T-C

60997422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591056-C-T

60997440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591079-G-C

http://identifiers.org/hco/1/GRCh38#60997572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97591170-A-C

60997572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591170-A-T

60997670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591251-G-A

60998916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591834-T-C

60998949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591853-G-C

60999045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591954-T-C

60999058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591967-G-A

60999058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97591967-G-C

http://identifiers.org/hco/1/GRCh38#60999320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97592210-A-C

60999488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592378-G-A

60999509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592388-G-T

60999758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592584-G-A

60999758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592584-G-T

61000143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592728-G-A

61000313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592914-G-A

61000328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97592921-A-G

61000815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97593962-G-T

61001102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594227-C-G

61001119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594242-T-C

61001229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594352-C-G

61001450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594617-C-T

61001477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594634-T-A

61001485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594642-G-C

61001545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594705-A-G

61001642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594758-T-C

61001872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97594914-G-A

http://identifiers.org/hco/1/GRCh38#61002008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97595052-C-A

61002008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595052-C-T

61002077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595088-G-A

61002525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595416-G-T

61002584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595473-A-G

61002872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595739-G-T

61002950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595815-C-G

61003077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97595943-G-A

61003246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97596092-A-T

61003557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97596386-G-C

61003608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97596518-A-G

61004449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97597326-C-T

http://identifiers.org/hco/1/GRCh38#61004534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97597418-A-C

61004702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97597566-G-A

61004971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97597770-C-G

61005331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598098-T-C

61005493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598261-T-C

61005812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598490-C-T

61005863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598541-A-G

61006105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598730-C-T

61006292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97598934-C-G

61006508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97599119-A-G

61006565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97599177-A-G

61007057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97599608-G-C

http://identifiers.org/hco/1/GRCh38#61008181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97600039-C-A

61008242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97600089-G-A

61008242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97600089-G-T

61008399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97600240-G-A

61009831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97600956-G-C

61009896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601007-G-T

61010065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601172-A-T

61010211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601298-C-T

61010289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601369-C-T

61010299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601379-G-A

61010741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601775-A-G

61010895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97601913-C-T

61010984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97602239-A-G

61011333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97602545-G-A

61011333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97602545-G-T

http://identifiers.org/hco/1/GRCh38#61011679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97602880-A-C

61011679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97602880-A-G

61011966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603165-C-T

http://identifiers.org/hco/1/GRCh38#61012063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97603258-C-A

61012145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603339-G-C

61012176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603370-T-C

61012201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603393-C-T

61012202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603394-G-A

61012202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603394-G-T

61012233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603416-G-A

http://identifiers.org/hco/1/GRCh38#61012316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97603624-C-A

61012321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603629-C-T

61012322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603630-C-T

61012384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603685-C-T

61012488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603790-T-C

http://identifiers.org/hco/1/GRCh38#61012496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97603798-C-A

http://identifiers.org/hco/1/GRCh38#61012497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97603799-A-C

61012551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603852-G-C

http://identifiers.org/hco/1/GRCh38#61012563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97603864-C-A

61012563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603864-C-G

61012563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97603864-C-T

61013008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604132-C-T

61013063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604183-A-G

61013275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604372-A-T

61013548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604613-A-G

61013663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604719-A-G

61013771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604817-G-C

61013771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604817-G-T

61013834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604869-C-T

61013855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604898-C-T

61013859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97604902-G-A

61014230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97605262-G-A

61014231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97605263-G-A

61014300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97605368-T-C

http://identifiers.org/hco/1/GRCh38#61015521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97607500-C-A

61015521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97607500-C-G

61015545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97607527-T-G

61015546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97607528-G-A

http://identifiers.org/hco/1/GRCh38#61015576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97607556-A-C

http://identifiers.org/hco/1/GRCh38#61015811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97607779-C-A

61015903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97607871-G-A

61015907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97607875-C-G

61016111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97608071-C-T

61016240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609472-A-G

61016469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609757-T-G

61016555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609842-T-A

61016637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609914-T-G

61016690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609955-G-A

61016713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609978-C-T

61016726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97609991-C-G

61016777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97610027-G-A

61017003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97610263-A-G

61017286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97610515-G-C

61017541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97610770-C-T

61017848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97611073-T-G

61018117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97611326-G-A

http://identifiers.org/hco/1/GRCh38#61018589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97612686-C-A

61018619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97612715-T-A

61018619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97612715-T-C

http://identifiers.org/hco/1/GRCh38#61018767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97612857-C-A

61018772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97612862-T-C

61018849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97612925-C-T

61018957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97613013-C-G

61019341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97613334-T-A

61019453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97613439-T-A

61020302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97619277-A-T

61020896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97619165-A-T

61021545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618511-A-G

61023891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97616738-T-G

http://identifiers.org/hco/1/GRCh38#61024229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97619926-A-C

http://identifiers.org/hco/1/GRCh38#61025298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97621841-C-A

61025588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97621918-G-A

61025588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97621918-G-C

http://identifiers.org/hco/1/GRCh38#61025810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97622105-A-C

61025883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622176-T-C

61026741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622476-G-A

61026741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622476-G-T

61026846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622581-G-A

61027095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622835-G-A

61027095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622835-G-C

61027095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97622835-G-T

61027989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97623361-G-T

61028004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97623380-T-A

61028004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97623380-T-C

61028028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97623401-G-A

http://identifiers.org/hco/1/GRCh38#61028622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97624069-A-C

61028856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624230-C-T

61029214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624409-G-A

61029214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624409-G-C

61029433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624564-T-C

61029576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624698-T-C

61029585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624707-C-T

61029726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624830-T-C

61029784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97624887-C-T

http://identifiers.org/hco/1/GRCh38#61030462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97625183-A-C

61030472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97625193-G-T

61031162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97625596-C-T

61031348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97625752-C-T

61031351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97625755-T-A

61031351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97625755-T-C

61041397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97632724-G-A

61041876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97632887-G-A

61041876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97632887-G-T

61041897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97632910-T-A

61041897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97632910-T-C

61042189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633209-G-A

61042219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633238-G-A

61042293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633312-T-C

61042395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633448-G-C

61042655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633708-A-G

61042677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633730-G-A

61042728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633780-T-G

61042925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633977-A-T

61042942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97633994-G-T

http://identifiers.org/hco/1/GRCh38#61042967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97634014-C-A

61042985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634032-C-T

61043035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634116-G-A

61043085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634192-A-G

61043162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634267-C-T

61043554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634572-C-T

61043590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634600-C-T

61043619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634629-C-T

61043634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634646-G-A

61043646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634658-G-A

61043682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634712-G-A

61043729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634751-G-A

61043729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97634751-G-C

61044054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97635061-A-T

61044270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97635354-A-G

61044272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97635356-A-G

61044610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97635608-T-C

61044627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97635622-T-G

61046128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97636712-C-T

61046229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97636807-C-T

61046443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97637059-C-G

61046503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97637119-A-T

61046732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97637696-T-C

61046940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97637980-A-T

61049899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639241-G-T

61049981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639322-G-A

61050379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639647-G-T

61050393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639651-C-T

61050603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639826-G-C

61050755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97639875-G-A

61051088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640144-G-C

http://identifiers.org/hco/1/GRCh38#61051121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97640177-C-A

61051186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640209-A-G

61051318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640345-A-G

61051324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640348-G-A

61051324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640348-G-T

61051383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640414-G-A

61052048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97640979-T-C

61052209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641127-A-G

61052260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641178-C-T

61052326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641256-C-G

61052326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641256-C-T

61052377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641305-C-T

61052390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641313-C-T

61052404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641327-G-A

61052448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641372-G-A

61052449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641373-A-T

61052614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641523-A-G

61052928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641726-G-T

61053117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97641961-A-T

61053224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97642048-T-C

61053490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97642292-G-A

61053576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97642379-T-A

61053576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97642379-T-C

http://identifiers.org/hco/1/GRCh38#61053800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97642543-C-A

61054082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97642819-G-T

http://identifiers.org/hco/1/GRCh38#61054083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97642820-C-A

61054536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643236-A-G

http://identifiers.org/hco/1/GRCh38#61054538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97643238-C-A

61054943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643643-A-G

61055078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643778-T-G

http://identifiers.org/hco/1/GRCh38#61055102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97643801-C-A

61055159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643860-G-T

61055163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643864-C-G

61055163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97643864-C-T

61055305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644009-G-A

61055322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644026-T-C

61055473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644159-G-A

61055473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644159-G-T

61055545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644228-T-C

61055665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644376-T-G

61055916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644599-A-G

61055960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644640-T-C

61056031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97644706-G-T

http://identifiers.org/hco/1/GRCh38#61056878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#97645528-C-A

61056879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40401
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97645529-A-G