27612105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132728522-G-C

27612313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132728297-G-A

27612374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132728244-A-G

27612383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132728235-G-A

http://identifiers.org/hco/1/GRCh38#27612715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132727953-A-C

27612841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727728-G-A

27612841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727728-G-T

27612872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727695-G-T

27612881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727686-G-A

27612881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727686-G-T

27612896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727670-G-A

27612896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 3 prime UTR variant
orthologous variants: 132727670-G-C

27612978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132727588-T-C

27613177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132727376-G-A

27613204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132727358-C-T

27613206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132727356-T-A

27613372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132727197-G-A

27614288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725931-A-G

27614288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725931-A-T

http://identifiers.org/hco/1/GRCh38#27614305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132725914-C-A

27614305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725914-C-T

27614455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: synonymous variant
orthologous variants: 132725778-C-T

27614605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725620-A-T

27614610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725615-G-C

27614648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725576-G-T

27614702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725505-G-C

27614702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725505-G-T

27614757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, undefined
orthologous variants: 132725445-G-A

27614757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, undefined
orthologous variants: 132725445-G-T

27614908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132725295-A-G

http://identifiers.org/hco/1/GRCh38#27614999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132725204-C-A

27615029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, undefined
orthologous variants: 132725176-C-T

27615046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, undefined
orthologous variants: 132725166-G-A

27615138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132725112-C-T

27615250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, undefined
orthologous variants: 132724981-C-T

http://identifiers.org/hco/1/GRCh38#27615287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724964-C-A

27615287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724964-C-T

http://identifiers.org/hco/1/GRCh38#27615348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724927-C-A

27615348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724927-C-T

http://identifiers.org/hco/1/GRCh38#27615361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724919-C-A

27615361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724919-C-T

27615498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: synonymous variant
orthologous variants: 132724816-C-G

http://identifiers.org/hco/1/GRCh38#27615643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724647-C-A

27615643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724647-C-G

27615643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724647-C-T

http://identifiers.org/hco/1/GRCh38#27615668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724602-C-A

27615668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724602-C-T

27615712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724562-C-T

27615751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724523-C-T

http://identifiers.org/hco/1/GRCh38#27615781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724493-A-C

27615781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724493-A-G

27615784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724490-G-A

27615784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724490-G-T

27615790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724484-G-A

27615790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132724484-G-T

http://identifiers.org/hco/1/GRCh38#27615894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724375-C-A

http://identifiers.org/hco/1/GRCh38#27615910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132724370-A-C

27615910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724370-A-G

27615910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724370-A-T

27615955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132724322-G-T

http://identifiers.org/hco/1/GRCh38#27616711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132722491-C-A

27616711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722491-C-T

http://identifiers.org/hco/1/GRCh38#27616721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132722483-C-A

27616721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722483-C-T

27616729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722475-A-G

27616733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722471-T-G

27616765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722450-T-A

27616919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132722314-C-T

27617134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132722113-C-G

http://identifiers.org/hco/1/GRCh38#27617310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132721942-C-A

27617310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721942-C-T

27617319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721934-G-T

27617356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721897-T-C

27617356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721897-T-G

http://identifiers.org/hco/1/GRCh38#27617365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132721888-A-C

http://identifiers.org/hco/1/GRCh38#27617390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132721864-C-A

27617407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721848-G-A

27617460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721794-G-T

27617467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721786-G-C

27617892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721088-A-G

27617921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721055-G-A

27617947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132721035-A-T

27618102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132720867-A-G

27618160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132720811-G-C

27618218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132720759-G-A

27618220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132720757-G-C

http://identifiers.org/hco/1/GRCh38#27618875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132719260-C-A

27619082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132719058-G-T

27619522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132718959-C-T

27619572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132718924-G-T

27619681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132718830-A-G

http://identifiers.org/hco/1/GRCh38#27619760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132718750-C-A

27619879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132718620-C-G

27621457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132716191-G-C

27621457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132716191-G-T

27621490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132716158-G-C

27621494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132716154-T-C

27621494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132716154-T-G

27621619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense variant
orthologous variants: 132716030-C-T

27621655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 132715994-T-G

http://identifiers.org/hco/1/GRCh38#27621668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132715981-A-C

27621768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715902-T-C

http://identifiers.org/hco/1/GRCh38#27622230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132715350-A-C

27622233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715347-G-A

27622240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715341-G-A

27622245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715338-C-T

27622258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715324-C-T

27622261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715303-C-T

http://identifiers.org/hco/1/GRCh38#27622270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132715294-C-A

27622276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715288-G-A

27622276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132715288-G-T

27622654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714819-C-T

27622965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714678-A-G

27623019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714624-G-T

27623166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714476-G-T

27623225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714421-A-T

27623231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714415-G-T

http://identifiers.org/hco/1/GRCh38#27623237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132714409-C-A

27623237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714409-C-T

27623262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714344-G-A

http://identifiers.org/hco/1/GRCh38#27623270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132714336-A-C

http://identifiers.org/hco/1/GRCh38#27623285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132714321-C-A

27623285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714321-C-G

27623285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: 132714321-C-T

http://identifiers.org/hco/1/GRCh38#27623346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132714249-A-C

http://identifiers.org/hco/1/GRCh38#27623438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132714167-C-A

27623438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132714167-C-T

http://identifiers.org/hco/1/GRCh38#27623557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132713790-C-A

27623557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132713790-C-T

27623686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132713666-C-T

27623788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132713594-A-G

27623811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132713571-G-A

27624027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132713333-T-A

http://identifiers.org/hco/1/GRCh38#27624044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132713316-C-A

27624044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132713316-C-G

27624044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132713316-C-T

http://identifiers.org/hco/1/GRCh38#27624062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132713301-C-A

27624062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132713301-C-T

27624172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713209-G-T

27624655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712034-A-G

http://identifiers.org/hco/1/GRCh38#27625112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132711500-C-A

27625143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132711469-G-A

27625143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132711469-G-T

27625267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132711342-G-T

27625277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711332-T-C

27625278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711331-T-C

27625319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711289-C-T

27625343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711265-C-T

27625363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132711247-C-T

27625521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132711052-C-T

http://identifiers.org/hco/1/GRCh38#27625995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710698-C-A

27625995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710698-C-T

http://identifiers.org/hco/1/GRCh38#27625996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710697-C-A

27625996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710697-C-G

27625996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710697-C-T

http://identifiers.org/hco/1/GRCh38#27626040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710653-A-C

27626040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710653-A-G

27626247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132710438-C-T

27626302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710382-G-A

27626302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710382-G-C

http://identifiers.org/hco/1/GRCh38#27626308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710376-C-A

27626308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710376-C-T

27626343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710332-A-G

27626388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710318-G-T

http://identifiers.org/hco/1/GRCh38#27626445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710295-C-A

27626445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710295-C-T

http://identifiers.org/hco/1/GRCh38#27626505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710247-C-A

27626505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132710247-C-G

27626509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132710243-T-C

27626604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132710167-G-A

27626604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132710167-G-T

http://identifiers.org/hco/1/GRCh38#27626618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710153-C-A

27626618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710153-C-T

http://identifiers.org/hco/1/GRCh38#27626621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132710150-C-A

27626621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710150-C-T

27626637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710134-G-A

27626637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710134-G-T

27626645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710126-C-T

27626657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132710114-G-T

27626687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710085-G-A

27626857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709898-G-A

27626861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709894-G-C

http://identifiers.org/hco/1/GRCh38#27628468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132709374-C-A

27628562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709336-T-C

27628704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709205-C-G

27628720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709194-G-A

27628875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709046-T-C

27629122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708858-G-A

27630215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132706570-G-A

27630287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132706480-T-C

27630328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132706433-C-T

27630702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132706166-G-T

27631270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132704842-C-T

27631278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704820-C-G

27631571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132704560-A-G

27631675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132704474-C-G

27631711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704438-C-T

27631880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132704278-T-C

27631914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704249-G-A

27632246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704006-C-T

27632248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704004-T-C

27632310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132703971-G-A

27632935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132703453-G-A

27633456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132703066-C-T

27633913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702704-C-G

27634248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132702385-G-A

27634404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132702228-C-T

27634438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132702190-G-C

27634484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702166-T-C

27634519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702138-G-A

http://identifiers.org/hco/1/GRCh38#27634759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132701890-C-A

27634759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132701890-C-T

27634800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701837-A-T

27634813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701824-T-A

27634967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701671-A-G

27635003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701640-A-G

http://identifiers.org/hco/1/GRCh38#27635010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132701633-C-A

27635010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701633-C-T

27635025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701618-T-C

27635131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132701500-G-A

27635137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5 prime UTR variant
orthologous variants: 132701494-G-A

27635137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3697
most severe consequence: 5 prime UTR variant
orthologous variants: 132701494-G-T