http://identifiers.org/hco/19/GRCh38#7830241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4216600-C-A

7830241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 5 prime UTR variant
orthologous variants: 4216600-C-T

7830509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4216889-G-A

7830509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4216889-G-C

7830967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4217332-C-T

7831055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4217429-A-G

7831348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4217673-C-T

http://identifiers.org/hco/19/GRCh38#7831388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4217712-A-C

7831725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4218067-G-T

http://identifiers.org/hco/19/GRCh38#7831996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4218358-C-A

7831998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4218360-C-T

7833982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4220230-C-T

7834031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4220280-G-A

7834559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4222039-G-A

7834611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4222071-G-A

7835712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4223585-G-A

7835712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4223585-G-C

7841375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4229224-G-T

7841528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4229370-C-T

7844485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4230179-A-G

7844602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4230282-T-C

7844602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4230282-T-G

7844852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4230905-G-A

http://identifiers.org/hco/19/GRCh38#7845153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4231199-C-A

7845153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4231199-C-T

7845154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4231200-G-A

7845154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4231200-G-C

7845310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4231351-G-A

7845332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4231382-G-A

http://identifiers.org/hco/19/GRCh38#7845347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4231397-C-A

http://identifiers.org/hco/19/GRCh38#7845649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4232805-A-C

7846196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233308-G-A

7846350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233326-G-A

7846350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233326-G-T

7846352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233328-G-A

7846352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233328-G-T

7846412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233385-G-A

7846412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233385-G-C

7846412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233385-G-T

http://identifiers.org/hco/19/GRCh38#7846474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4233471-C-A

7846474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4233471-C-T

http://identifiers.org/hco/19/GRCh38#7846537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4233528-C-A

7846537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 5 prime UTR variant
orthologous variants: 4233528-C-T

7846605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4233596-C-T

http://identifiers.org/hco/19/GRCh38#7846699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4233682-A-C

7847732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 4235961-G-A

7847732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 4235961-G-C

7847789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4236018-T-C

7847831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4236060-G-A

7848133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4236305-G-A

7848176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4236335-G-A

7848176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4236335-G-T

7848204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4236357-G-A

7848320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4236531-G-C

7848772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237070-A-G

7848811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237114-G-A

7848811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237114-G-T

7848828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237130-T-A

7848828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237130-T-C

7848847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237149-G-A

7848847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237149-G-T

7848854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237156-G-A

7848854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237156-G-T

http://identifiers.org/hco/19/GRCh38#7848891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4237198-C-A

7848891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237198-C-T

7848894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237201-G-A

7848894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4237201-G-T

7849172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4237498-C-T

7849221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4237538-G-C

7849221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4237538-G-T

http://identifiers.org/hco/19/GRCh38#7849412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4237697-C-A

7849412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4237697-C-G

7849412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4237697-C-T

http://identifiers.org/hco/19/GRCh38#7849422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4237707-A-C

http://identifiers.org/hco/19/GRCh38#7849879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4238145-C-A

http://identifiers.org/hco/19/GRCh38#7849961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4238247-C-A

7849961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4238247-C-T

7850032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4238322-G-A

7850032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4238322-G-T

7850701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239544-G-A

7850701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239544-G-C

7850716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4239554-C-T

7851288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241125-G-A

7851288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241125-G-C

7851301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241139-A-G

7851318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241154-A-G

7851318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241154-A-T

7851335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241171-T-C

7851380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241217-C-G

7851380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241217-C-T

7851397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241222-C-T

7851484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4241287-A-G

http://identifiers.org/hco/19/GRCh38#7851738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4241642-C-A

7851738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4241642-C-T

7851796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241699-G-T

7851874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4241855-A-G

7852002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242172-A-T

7852004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242174-A-G

7852102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242279-C-T

7852144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242331-C-G

7852204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242392-C-T

http://identifiers.org/hco/19/GRCh38#7852466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4242623-C-A

7852466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242623-C-G

http://identifiers.org/hco/19/GRCh38#7852496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4242653-C-A

7852743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242841-T-A

7852743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242841-T-C

7852743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242841-T-G

7852773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242875-C-T

7852925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242962-T-C

7853502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 4243549-G-A

7853502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 4243549-G-T

7853515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 4243563-G-A

7853515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 4243563-G-T

7853574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4243649-G-A

7853574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4243649-G-C

7853574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4243649-G-T

7853752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4243836-A-G

7853752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4243836-A-T

7853862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4243956-G-T

7853898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243992-G-T

7853930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4244020-C-T

7853999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244099-T-C

http://identifiers.org/hco/19/GRCh38#7855936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4250784-C-A

7855936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250784-C-T

http://identifiers.org/hco/19/GRCh38#7856005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4250858-A-C

7856005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250858-A-G

7856607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251505-C-T

http://identifiers.org/hco/19/GRCh38#7856721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4251627-A-C

7856729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251635-G-A

7857159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252003-T-A

http://identifiers.org/hco/19/GRCh38#7857209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4252053-C-A

7857209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252053-C-T

http://identifiers.org/hco/19/GRCh38#7857214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4252065-C-A

7857268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252109-G-A

7857268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252109-G-C

7857268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252109-G-T

7857402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252246-G-A

7857402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252246-G-T

7857493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252342-C-T

http://identifiers.org/hco/19/GRCh38#7857507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4252356-C-A

7857644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252479-T-G

7857952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252687-C-T

7858000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252748-A-G

http://identifiers.org/hco/19/GRCh38#7858092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#4252845-C-A

7858092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4252845-C-G

7858092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4252845-C-T

http://identifiers.org/hco/19/GRCh38#7858098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#4252853-C-A

7858098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4252853-C-T

7858124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4252870-A-G

http://identifiers.org/hco/19/GRCh38#7858307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#4253052-C-A

7858307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 4253052-C-G

http://identifiers.org/hco/19/GRCh38#7860494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4253448-C-A

7860494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253448-C-G

7860494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253448-C-T

7860523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253477-A-G

http://identifiers.org/hco/19/GRCh38#7860704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4253658-C-A

7860704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253658-C-G

7860704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253658-C-T

7860740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253736-G-A

7860740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253736-G-T

7860742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253738-G-A

7860742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253738-G-T

7860756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253774-G-T

7860762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253780-G-A

7860762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4253780-G-T

7861283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4254735-C-G

7861393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4254844-C-G

7861452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4254888-G-C

7861749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255196-G-C

7861749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255196-G-T

7861814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255258-G-A

7861814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255258-G-C

7861814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255258-G-T

7861822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255266-G-T

7861823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255267-G-A

7861823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255267-G-T

7861838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255281-T-C

http://identifiers.org/hco/19/GRCh38#7861840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4255283-C-A

7861840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255283-C-T

7861962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4255406-G-T

7862331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255763-C-T

http://identifiers.org/hco/19/GRCh38#7862343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4255775-C-A

7862343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4255775-C-T

7862843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256005-G-C

7862843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256005-G-T

7862933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256036-C-G

7862933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256036-C-T

7862998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4256082-A-G

7863055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4256139-G-A

7863055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, missense_variant
orthologous variants: 4256139-G-T

http://identifiers.org/hco/19/GRCh38#7863107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256178-C-A

7863107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256178-C-T

http://identifiers.org/hco/19/GRCh38#7863244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256291-C-A

7863244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4256291-C-T

7863274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256321-G-A

7863274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4256321-G-T

7863302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256346-G-A

7863302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256346-G-T

http://identifiers.org/hco/19/GRCh38#7863342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256391-C-A

7863342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, undefined
orthologous variants: 4256391-C-T

7863351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron_variant, undefined
orthologous variants: 4256400-C-T

7863380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256429-G-A

7863380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: intron variant
orthologous variants: 4256429-G-C

7863462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256534-G-A

7863462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256534-G-T

7863480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256552-G-A

7863480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256552-G-T

7863489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256561-G-A

7863489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256561-G-C

7863489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256561-G-T

http://identifiers.org/hco/19/GRCh38#7863622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256700-C-A

7863622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4256700-C-T

http://identifiers.org/hco/19/GRCh38#7863657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256735-C-A

7863657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4256735-C-G

7863657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: synonymous variant
orthologous variants: 4256735-C-T

7863668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4256746-T-C

7863683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: missense variant
orthologous variants: 4256764-G-T

http://identifiers.org/hco/19/GRCh38#7863753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256839-C-A

http://identifiers.org/hco/19/GRCh38#7863831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256906-C-A

7863831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4256906-C-T

http://identifiers.org/hco/19/GRCh38#7863846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256926-C-A

7863846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4256926-C-T

http://identifiers.org/hco/19/GRCh38#7863900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256960-C-A

7863900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4256960-C-T

http://identifiers.org/hco/19/GRCh38#7863904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4256964-C-A

7863904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4256964-C-G

7863904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4256964-C-T

7863968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257040-T-A

7863968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257040-T-C

7863986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257055-T-C

7864069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257131-G-C

7864069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257131-G-T

7864070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257132-G-A

7864070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257132-G-C

7864070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257132-G-T

7864471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257533-G-A

7864471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257533-G-T

7864475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257537-G-T

7864501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257569-C-T

7864603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257648-T-C

7864734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257783-T-C

http://identifiers.org/hco/19/GRCh38#7864796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4257844-C-A

7864801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257849-C-T

http://identifiers.org/hco/19/GRCh38#7864804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4257852-C-A

7864804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: 4257852-C-T

http://identifiers.org/hco/19/GRCh38#7864827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#4257874-C-A