38889902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 80614861-T-A

http://identifiers.org/hco/2/GRCh38#38889969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80614928-C-A

38890085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615032-T-C

38890118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615065-T-C

38890225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615167-C-T

38890387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615333-A-G

38890387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615333-A-T

38890597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615562-G-A

38890765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615726-T-C

38891011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80615959-C-T

38891115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616046-G-A

38891115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616046-G-T

http://identifiers.org/hco/2/GRCh38#38891134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80616069-A-C

38891134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616069-A-G

38891134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616069-A-T

38891419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616444-C-T

38891497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616538-G-A

38891572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616665-C-T

38891762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80616896-A-G

38892148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80617246-G-T

38892748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618187-A-G

38892792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618232-C-G

38892837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618272-G-A

38892943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618375-A-G

38893520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618606-T-A

38893529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618612-T-A

38893561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618626-A-G

38893644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618690-T-C

38893725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80618780-T-C

http://identifiers.org/hco/2/GRCh38#38894384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80619238-C-A

38894384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619238-C-T

http://identifiers.org/hco/2/GRCh38#38894525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80619358-C-A

38894686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619507-A-G

38894749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619558-A-G

38895001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619829-G-A

38895051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619883-G-T

38895107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80619927-C-T

38895265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80620104-T-A

38895265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80620104-T-G

38895322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80620124-A-T

38895386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80620214-A-G

http://identifiers.org/hco/2/GRCh38#38896116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80620829-A-C

38897640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80622560-C-T

38897717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80622625-T-A

38898368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623379-C-T

38898556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623531-A-G

38898556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623531-A-T

38898559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623533-A-G

38898659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623629-T-G

38898696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623661-T-C

38898763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80623728-T-C

38899163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624234-C-G

http://identifiers.org/hco/2/GRCh38#38899478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80624826-A-C

38899579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624916-G-A

38899580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624917-C-T

38899581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624918-G-A

38899582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624919-T-C

38899587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624924-C-G

38899587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80624924-C-T

38899699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625063-T-C

38899776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625140-G-A

38899837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625211-G-T

38899914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625251-C-G

38899941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625278-C-T

38901070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625803-A-G

http://identifiers.org/hco/2/GRCh38#38901076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80625809-C-A

38901076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625809-C-T

38901281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625870-G-A

38901357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625928-G-A

38901419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625987-G-C

38901433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80625989-C-T

38901538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626095-C-G

38901538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626095-C-T

38901636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626197-C-T

38901641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626202-T-C

http://identifiers.org/hco/2/GRCh38#38901796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80626372-A-C

38901798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626374-C-T

38902842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626724-G-A

38902917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80626749-A-G

38903237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627083-A-G

38903318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627254-T-G

38903328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627264-C-T

38903359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627293-A-G

38903359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627293-A-T

38903401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627319-A-G

38903523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627459-T-A

38903524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627460-A-G

38903527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627463-G-A

38903546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80627480-A-G

http://identifiers.org/hco/2/GRCh38#38903742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80627662-C-A

38904277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80628104-G-T

38904281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80628108-G-C

38906226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80628899-A-G

http://identifiers.org/hco/2/GRCh38#38906267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80628938-A-C

38906303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80628973-T-C

38907241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630358-A-G

http://identifiers.org/hco/2/GRCh38#38907424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80630518-C-A

38907424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630518-C-G

38907522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630616-G-C

38907528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630621-C-T

38907666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630773-G-T

38908092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80630979-T-G

38908146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631010-T-C

38908250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631113-A-G

38908262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631123-A-G

38908262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631123-A-T

38908343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631199-G-T

38908371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631227-C-T

38908457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631301-C-T

38908624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631443-A-G

38908638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631458-C-T

38908725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631545-C-G

38908725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631545-C-T

38908772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631589-G-C

38908883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631696-A-G

38908896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80631709-G-A

http://identifiers.org/hco/2/GRCh38#38908898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80631726-C-A

38909970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80632439-G-A

38909970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80632439-G-T

http://identifiers.org/hco/2/GRCh38#38910025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80632477-C-A

38910025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80632477-C-G

38910824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633519-T-C

38910852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633547-C-G

38910947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633630-C-G

http://identifiers.org/hco/2/GRCh38#38910989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80633668-C-A

38911073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633731-G-A

38911127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633781-T-A

38911197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633855-C-T

38911237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80633896-A-G

http://identifiers.org/hco/2/GRCh38#38911517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80634173-C-A

38911517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80634173-C-T

38911518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80634174-G-A

38911695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80634350-C-G

38911695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80634350-C-T

http://identifiers.org/hco/2/GRCh38#38911736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80634392-C-A

38912058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80635460-A-G

38912109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80635519-C-T

38912213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80635619-G-A

38912213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80635619-G-T

38912403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80635867-C-G

38916140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80641543-C-G

38918706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80641965-T-C

38918706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80641965-T-G

38919208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642518-A-G

38919218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642528-T-G

38919253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642562-G-A

38919253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642562-G-C

38919253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642562-G-T

38919294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642599-T-A

38919294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642599-T-G

http://identifiers.org/hco/2/GRCh38#38919343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80642646-C-A

38919354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642653-A-T

38919380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 80642679-T-C

38919404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, undefined
orthologous variants: 80642703-T-C

38919463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 80642762-A-G

38919499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642792-A-G

38919529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80642822-T-C

38920177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80643339-A-G

38920196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80643358-A-G

http://identifiers.org/hco/2/GRCh38#38920243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80643421-C-A

38920345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80643515-C-T

38920910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80643716-G-A

38920940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80643750-G-A

38921052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644374-A-G

38921158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644482-A-G

38921224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644549-G-A

38921224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644549-G-T

http://identifiers.org/hco/2/GRCh38#38921225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644550-C-A

38921225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644550-C-G

38921282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644606-A-G

http://identifiers.org/hco/2/GRCh38#38921289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644613-A-C

http://identifiers.org/hco/2/GRCh38#38921366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644690-C-A

38921366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 80644690-C-G

38921366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 80644690-C-T

http://identifiers.org/hco/2/GRCh38#38921367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80644691-C-A

38921367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 80644691-C-G

38921370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 80644694-G-T

38921488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644807-G-T

38921509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80644826-A-G

38922109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80645577-A-T

38922238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80645691-C-T

38922514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646441-C-T

38922515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646442-G-A

38922537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646462-G-T

http://identifiers.org/hco/2/GRCh38#38922611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80646531-C-A

38922653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646573-T-C

38922679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646599-T-C

38922727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646650-T-C

38922742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646665-T-C

38922904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80646828-T-A

38923092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647023-C-T

38923125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647060-G-T

38923168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647107-G-T

38923206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647130-G-A

38923224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647144-G-A

38923225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647145-A-T

http://identifiers.org/hco/2/GRCh38#38923284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80647193-C-A

38923284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647193-C-G

38923294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647203-C-T

38923348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647225-A-G

38923362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647239-A-T

38923448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80647327-C-G

38925408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80649699-A-G

38925408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80649699-A-T

38925450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80649738-A-T

38925533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80649830-G-C

38925602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80649897-G-T

38925793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80650269-G-C

38925817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80650292-C-T

38925931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80650408-G-T

38926084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80650553-A-G

38926103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80651066-G-A

38926164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 80651118-G-A

http://identifiers.org/hco/2/GRCh38#38926166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80651120-C-A

38926167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 80651121-C-T

38926306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80651259-C-T

38926314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80651267-A-G

38926353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80651298-G-A

38926476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80651417-T-C

38927182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80652575-A-T

38927332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80652724-A-G

38927370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80652771-T-C

38927644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80652971-C-T

38927657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80652983-C-G

38927691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653005-G-A

38927691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653005-G-C

38927773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653068-C-T

38927799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653094-T-G

38927909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653191-G-A

38928100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653382-A-G

38928265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653567-T-A

38928356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80653607-C-T

38928569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654060-C-T

38928645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654301-A-T

38928664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654313-T-C

38928669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654318-G-T

38928682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654331-T-A

38928717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, undefined
orthologous variants: 80654359-G-T

38929101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654744-A-G

38929136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654779-C-G

http://identifiers.org/hco/2/GRCh38#38929180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80654793-C-A

38929180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654793-C-T

38929510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654842-T-A

38929619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654945-A-G

38929624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654950-T-A

38929636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80654967-A-G

38929689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655017-T-C

38929842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655170-T-G

38929916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655245-G-A

38929916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655245-G-T

38929951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655280-G-C

38929951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655280-G-T

http://identifiers.org/hco/2/GRCh38#38930036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80655881-C-A

38930036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655881-C-T

38930165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80655998-A-G

38930208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656042-C-T

38930721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656253-G-C

38930721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656253-G-T

38930751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656292-T-A

38930810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656351-C-T

http://identifiers.org/hco/2/GRCh38#38930968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80656651-C-A

38931048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80656794-T-C

38931347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657115-A-G

38931347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657115-A-T

38931385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657156-A-G

http://identifiers.org/hco/2/GRCh38#38931419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80657190-A-C

http://identifiers.org/hco/2/GRCh38#38931504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80657269-A-C

38931607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657363-G-A

38931828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657573-T-A

38931838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657583-C-T

38931846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657591-C-T

38931873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657622-G-A

38931987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657777-T-C

http://identifiers.org/hco/2/GRCh38#38932089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80657873-A-C

38932447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80657910-T-A

38933115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80658789-A-G

http://identifiers.org/hco/2/GRCh38#38933146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80658820-C-A

38933345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80659001-C-T

http://identifiers.org/hco/2/GRCh38#38935662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80659990-C-A

38935662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80659990-C-T

http://identifiers.org/hco/2/GRCh38#38935694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80660031-C-A

38935694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80660031-C-T

38935745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80660080-C-T

38936297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80661254-C-G

38936589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80661759-G-T

38936760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80661902-G-A

38936762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80661904-G-A

38937611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80662667-A-G

http://identifiers.org/hco/2/GRCh38#38937613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80662669-A-C

http://identifiers.org/hco/2/GRCh38#38937669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80662714-C-A

http://identifiers.org/hco/2/GRCh38#38937693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80662731-C-A

38937693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80662731-C-T

http://identifiers.org/hco/2/GRCh38#38937694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80662732-A-C

38937694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80662732-A-G

38937742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80662785-G-A

38938025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80663031-G-C

38938122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80663139-T-G

38943869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80667718-A-G

38944100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80667957-A-T

38944107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80667964-G-A

38944107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80667964-G-T

38944860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668230-T-C

38945067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668377-A-G

38945068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668378-T-C

38945209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668505-T-G

38945213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668509-C-G

http://identifiers.org/hco/2/GRCh38#38945285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80668575-A-C

38945400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80668778-G-C

38947847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80670005-G-A

38948304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670796-G-A

38948311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670803-A-G

38948361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670834-T-A

38948361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670834-T-G

38948408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670879-C-G

38948408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80670879-C-T

38949057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671418-A-T

38949153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671523-A-T

38949460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671825-C-T

38949504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671875-C-T

38949517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671888-C-G

38949517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80671888-C-T

38949676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80672014-G-A

38949676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80672014-G-T

38950157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80672275-G-A

38950218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80672332-C-G

38950371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672434-C-T

38950772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672510-C-T

38950894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672605-A-G

38950938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672647-C-T

38950970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672679-G-A

38950970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672679-G-C

38950970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672679-G-T

38950995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80672704-C-T

http://identifiers.org/hco/2/GRCh38#38951180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80672879-C-A

38951180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672879-C-G

38951200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672899-T-A

38951200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672899-T-C

http://identifiers.org/hco/2/GRCh38#38951208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80672907-C-A

38951208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80672907-C-T

http://identifiers.org/hco/2/GRCh38#38951244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80672946-C-A

38951625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673155-A-G

http://identifiers.org/hco/2/GRCh38#38951634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80673164-A-C

38951653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673179-C-T

38951982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673490-G-C

38952068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673579-C-T

38952260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673731-A-T

38952264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673735-G-C

38952281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673753-T-A

38952304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80673772-A-G

38952338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80673803-G-C

38952918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674388-C-T

38952977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674468-G-A

38952988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674488-C-T

38953185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80674705-T-A

38953185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80674705-T-G

http://identifiers.org/hco/2/GRCh38#38953200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80674720-C-A

http://identifiers.org/hco/2/GRCh38#38953282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80674802-C-A

38953282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674802-C-T

38953288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674806-G-A

http://identifiers.org/hco/2/GRCh38#38953309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80674828-C-A

38953309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674828-C-T

38953335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674853-T-A

38953338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674862-G-A

38953338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674862-G-T

38953350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674874-G-A

38953350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80674874-G-T

38953677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675149-G-C

38954196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675455-C-T

http://identifiers.org/hco/2/GRCh38#38954222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80675481-C-A

38954222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675481-C-T

38954280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675544-G-C

38954335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675576-G-T

http://identifiers.org/hco/2/GRCh38#38954358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80675599-C-A

38954358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675599-C-T

38954364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675605-T-C

38954393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: synonymous variant
orthologous variants: 80675634-T-C

38954467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675708-G-T

38954516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675749-G-T

38954541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675773-G-C

38954541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675773-G-T

38954602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675840-A-T

http://identifiers.org/hco/2/GRCh38#38954603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80675841-C-A

38954606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675844-A-G

38954614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675852-C-T

38954659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675870-A-G

38954659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675870-A-T

38954962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80675892-C-T

http://identifiers.org/hco/2/GRCh38#38955023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80675959-C-A

http://identifiers.org/hco/2/GRCh38#38955138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80676070-C-A

38955318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80676243-T-A

38955368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80676300-T-A

38956753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677566-T-C

38956762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677575-G-T

38956853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677654-T-G

38956860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677661-C-T

http://identifiers.org/hco/2/GRCh38#38956886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80677687-C-A

38956886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677687-C-G

38956886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677687-C-T

38957039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: synonymous variant
orthologous variants: 80677840-G-A

38957197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80677977-G-T

38957222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80678002-C-T

38957488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80678215-A-G

http://identifiers.org/hco/2/GRCh38#38957771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80678475-C-A

http://identifiers.org/hco/2/GRCh38#38957807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80678504-C-A

38957807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80678504-C-T

http://identifiers.org/hco/2/GRCh38#38957838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80678535-A-C

38957838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80678535-A-G

38957838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron variant
orthologous variants: 80678535-A-T

38957937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80678606-T-A

38957937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80678606-T-C

38957944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80678613-G-T

38957986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80678656-C-T

38958163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80678829-C-G

38958163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80678829-C-T

38958201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80678867-A-G

38958240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80678906-T-C

38958240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80678906-T-G

http://identifiers.org/hco/2/GRCh38#38958273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80678934-C-A

38958273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80678934-C-T

38958454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80679294-A-T

38958513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80679345-T-C

http://identifiers.org/hco/2/GRCh38#38959176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679647-C-A

http://identifiers.org/hco/2/GRCh38#38959184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679656-C-A

http://identifiers.org/hco/2/GRCh38#38959207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679676-A-C

38959207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80679676-A-G

http://identifiers.org/hco/2/GRCh38#38959282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679741-C-A

38959282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80679741-C-T

http://identifiers.org/hco/2/GRCh38#38959361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679809-C-A

38959386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679836-A-G

38959440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679863-G-T

38959531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679950-G-C

38959531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679950-G-T

http://identifiers.org/hco/2/GRCh38#38959547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679968-C-A

38959547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679968-C-T

http://identifiers.org/hco/2/GRCh38#38959549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679970-C-A

38959570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679991-G-A

38959570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679991-G-T

http://identifiers.org/hco/2/GRCh38#38959574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80679995-C-A

38959574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80679995-C-G

38959621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680066-G-A

38959621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680066-G-T

38959726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680305-G-C

38959752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80680331-A-G

http://identifiers.org/hco/2/GRCh38#38959776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80680366-A-C

38959776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680366-A-G

38959783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680373-A-G

38959982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80680562-C-T

38960054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80680634-T-C

38960111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80680691-G-T

http://identifiers.org/hco/2/GRCh38#38960178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80680758-C-A

38960178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680758-C-G

38960183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80680763-C-G

38960201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80680781-G-A

38960201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680781-G-T

38960295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680875-A-G

38960295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80680875-A-T

http://identifiers.org/hco/2/GRCh38#38960504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681087-C-A

38960504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80681087-C-T

http://identifiers.org/hco/2/GRCh38#38960546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681129-C-A

38960546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80681129-C-G

38960546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80681129-C-T

http://identifiers.org/hco/2/GRCh38#38960561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681144-C-A

38960561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80681144-C-G

38960561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80681144-C-T

http://identifiers.org/hco/2/GRCh38#38960564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681147-C-A

38960564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80681147-C-G

38960564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80681147-C-T

38960668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681251-A-G

38960677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681257-G-A

38960677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681257-G-C

38960677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681257-G-T

http://identifiers.org/hco/2/GRCh38#38960681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681261-C-A

38960681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681261-C-T

38960734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681311-A-G

38960840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681364-C-T

38961173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681589-A-G

38961261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681665-T-C

38961493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681818-G-C

38961531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681858-G-A

38961540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681867-G-A

38961578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681894-G-C

38961642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80681955-T-G

http://identifiers.org/hco/2/GRCh38#38961674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80681989-C-A

38961715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80682001-G-A

38961772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80682059-G-A

38961838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80682126-G-C

38961981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80682267-C-G

38961981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80682267-C-T

38962254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80682523-C-T

38962319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80682579-A-G

38962356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80682624-T-C

38962453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80682726-A-G

38963548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683849-G-C

38963548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683849-G-T

38963570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683869-T-A

38963586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80683885-A-G

http://identifiers.org/hco/2/GRCh38#38964794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80684308-C-A

38964798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684312-C-T

38964849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684359-T-A

38964951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684473-T-C

38964980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80684502-T-G

http://identifiers.org/hco/2/GRCh38#38965002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80684524-C-A

38966234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80688994-C-T

http://identifiers.org/hco/2/GRCh38#38966269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80689028-C-A

38966269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689028-C-T

38966540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689194-G-A

38966560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689215-G-A

38966560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689215-G-C

38966717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689355-T-A

38967202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689793-T-C

38967260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689844-G-A

38967260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80689844-G-C

38967493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690104-T-C

38968149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690435-C-G

http://identifiers.org/hco/2/GRCh38#38968438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80690719-C-A

38968575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80690859-C-T

38968790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691043-T-C

38968955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691218-G-A

38969083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691291-C-T

38969112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691319-C-T

38969177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691455-G-C

http://identifiers.org/hco/2/GRCh38#38969242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80691507-C-A

38969314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691558-C-T

38969526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80691768-C-T

38969725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80691946-T-C

38969827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692047-T-C

38970033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692302-T-A

38970033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692302-T-G

38970476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692706-C-G

38970501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692732-T-C

38970527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692759-T-A

38970536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692768-T-C

38970684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80692882-A-G

http://identifiers.org/hco/2/GRCh38#38972055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80693979-A-C

38972055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693979-A-G

38972077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80693999-A-G

38972336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694250-A-T

38972378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694285-A-G

38972424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694337-T-C

38972519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80694422-C-G

38973374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80695344-T-C

http://identifiers.org/hco/2/GRCh38#38974334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80696249-C-A

http://identifiers.org/hco/2/GRCh38#38974427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80696337-A-C

38974565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696452-G-A

38974565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696452-G-T

38974609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696476-A-G

38974680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696539-G-T

38974754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696654-C-G

http://identifiers.org/hco/2/GRCh38#38974777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80696680-C-A

38974777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696680-C-T

38974862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696764-T-C

38974936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696839-G-A

http://identifiers.org/hco/2/GRCh38#38975033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80696939-C-A

38975033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80696939-C-T

38975144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80697011-A-G

38975159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80697026-G-T

38975392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37252
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80697252-G-C