112275949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 5 prime UTR variant
orthologous variants: 128809680-G-A

112275949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 5 prime UTR variant
orthologous variants: 128809680-G-T

112276243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128809975-C-T

112276519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, undefined
orthologous variants: 128810280-G-C

112276679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128810392-T-C

112276825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128810519-A-G

112277157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128810861-G-C

112277280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128810979-T-A

112277450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128811224-C-G

112278022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812152-G-A

112278051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812176-A-G

112278069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812190-C-T

112278119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812227-T-C

112278154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812277-A-T

112278198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812315-T-C

112278209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812326-T-C

112278662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128812451-G-T

112279368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128813487-G-A

112279469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128813581-T-C

112279536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128813647-A-G

112281123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128814191-G-A

112281362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128814454-A-T

112282090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128815392-T-C

112282092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128815394-T-G

112282328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128815671-T-G

112282992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128816359-C-G

http://identifiers.org/hco/2/GRCh38#112283146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128816523-C-A

112283364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128816724-C-T

112283650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128816976-T-C

112283861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128817105-A-G

112283861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128817105-A-T

112284305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128817515-A-G

112284667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128817797-G-A

112288084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820525-G-A

112288197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820627-G-A

112288207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820637-A-T

112288370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820753-T-C

112288370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820753-T-G

112290251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820917-T-A

112290269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128820935-A-T

112292340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128823610-C-T

112292825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825104-C-G

112292860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825138-C-T

112292946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825223-A-T

112293007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825308-A-G

112293015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825316-A-T

112293223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825620-C-G

112293229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825626-T-G

112293333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128825968-A-G

112293406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826033-A-G

112293611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826639-T-C

112293614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826642-C-G

112293614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826642-C-T

112293903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826892-A-G

112293962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128826953-A-G

112294119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128827103-A-T

112294209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128827191-A-G

112294267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128827246-A-T

http://identifiers.org/hco/2/GRCh38#112294537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128827473-A-C

112295181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828798-G-A

112295274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828885-C-T

112295275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828886-G-A

112295275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828886-G-C

112295298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828908-G-A

112295298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128828908-G-C

112295651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128829997-T-G

112295658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830004-A-G

112295705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830051-G-A

112295950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830215-T-A

112296112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830390-T-C

112296200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830475-C-T

112296271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830545-A-G

112296448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128830706-A-G

112296964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128831833-A-G

112296971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128831840-A-G

112297025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128831890-G-T

112297591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832366-C-G

112297795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832538-G-T

112299516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832688-T-C

112299644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832804-A-G

112299660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832817-G-A

112299697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832854-T-C

http://identifiers.org/hco/2/GRCh38#112299710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128832867-C-A

112299710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832867-C-T

112299718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832875-G-T

112299819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128832976-T-C

112300039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128833206-A-G

http://identifiers.org/hco/2/GRCh38#112300045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128833212-C-A

112300045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128833212-C-G

112302347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128834091-C-T

112302954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128834841-C-T

112303006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128834893-A-G

112303380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835225-A-T

112303388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835233-T-C

112303720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835521-T-C

112303757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835556-G-A

112303794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835594-T-G

112303798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835598-C-T

112304122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128835812-G-T

112304416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128836147-G-T

112309626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839280-G-A

http://identifiers.org/hco/2/GRCh38#112309628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128839282-A-C

112309669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839318-A-G

112309802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839454-G-A

http://identifiers.org/hco/2/GRCh38#112309837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128839477-C-A

112309892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128839532-A-G

112309917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128839557-A-G

http://identifiers.org/hco/2/GRCh38#112310178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128839805-A-C

112310178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839805-A-G

112310179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839806-G-C

http://identifiers.org/hco/2/GRCh38#112310284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128839899-C-A

112310300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839915-G-A

112310300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839915-G-T

112310338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128839954-G-T

112310472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128840064-G-A

112310597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128840418-T-A

112311390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128842721-G-A

http://identifiers.org/hco/2/GRCh38#112311464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128842794-A-C

112311516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128842852-G-A

112311516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128842852-G-C

112311623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128842953-C-T

http://identifiers.org/hco/2/GRCh38#112311743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128844000-C-A

112311743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128844000-C-G

112311743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128844000-C-T

112311916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128844177-A-G

112311998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128844257-G-A

112312211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128844478-A-T

112313030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845446-G-A

112313215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845625-A-G

112313219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845629-T-C

112313242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845651-A-G

112313592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845941-G-T

112313644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128845993-A-G

112315914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847296-A-T

112315936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847318-T-G

112315957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847340-T-C

112316024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847405-T-A

112316049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847421-A-G

112316049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847421-A-T

112316059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847431-G-A

112316139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847598-A-G

112316350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847800-G-A

112316350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847800-G-T

112316372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128847822-T-C

112316702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848137-G-A

112316702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848137-G-T

112316819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848337-T-G

http://identifiers.org/hco/2/GRCh38#112316873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128848391-C-A

112316995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848484-T-G

http://identifiers.org/hco/2/GRCh38#112317088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128848541-C-A

112317088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848541-C-T

http://identifiers.org/hco/2/GRCh38#112317198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128848610-C-A

112317198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848610-C-G

112317198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848610-C-T

112317202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848614-T-C

http://identifiers.org/hco/2/GRCh38#112318271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128848984-C-A

112318274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128848987-G-A

112318468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128849163-G-C

112321826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128852406-T-C

112321850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128852430-G-A

112321850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128852430-G-C

112321850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128852430-G-T

112322714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128853652-T-G

112322918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853854-T-C

112322940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853872-T-C

http://identifiers.org/hco/2/GRCh38#112322987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128853885-A-C

112322987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853885-A-T

112323004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853902-T-G

112323018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853915-A-G

112323044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128853940-T-C

112323120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128854015-A-G

112323530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128855327-G-A

112323625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128855420-C-G

112323786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128855547-A-G

112323983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128855679-C-G

112324156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856260-C-G

112324194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128856298-A-G

http://identifiers.org/hco/2/GRCh38#112324223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128856327-A-C

112324223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856327-A-G

112324223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856327-A-T

112324263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128856367-C-T

112324277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856381-A-G

112324277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856381-A-T

112324288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128856392-G-A

112324582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128856677-C-T

112324605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128856700-C-T

112324832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128856935-A-G

112324832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128856935-A-T

112324875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128856986-G-T

112324892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128857047-G-A

http://identifiers.org/hco/2/GRCh38#112324948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128857191-C-A

112324948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128857191-C-T

112324949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128857192-A-G

112325013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128857369-A-G

112325124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128857480-A-G

http://identifiers.org/hco/2/GRCh38#112325174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128857530-A-C

112325174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128857530-A-G

112330892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128857994-T-A

112330895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: intron variant
orthologous variants: 128857997-A-G

112331292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128858329-G-A

112331603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858640-G-A

112331603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858640-G-T

112331681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858715-T-C

http://identifiers.org/hco/2/GRCh38#112331709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128858743-A-C

112331747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858781-A-G

112331777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858811-A-T

112331928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128858962-G-A

112331928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128858962-G-T

http://identifiers.org/hco/2/GRCh38#112331940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128858974-C-A

112331960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128858994-C-T

112332086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: synonymous variant
orthologous variants: 128859117-A-G

112332097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense variant
orthologous variants: 128859128-C-T

http://identifiers.org/hco/2/GRCh38#112332214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128859242-C-A

http://identifiers.org/hco/2/GRCh38#112332222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128859250-A-C

112332222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128859250-A-G

112332225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128859253-G-A

112332225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128859253-G-C

112332225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128859253-G-T

http://identifiers.org/hco/2/GRCh38#112332528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128859538-A-C

112332528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128859538-A-G

112332623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128859634-T-A

http://identifiers.org/hco/2/GRCh38#112332683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128859694-C-A

112332683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128859694-C-T

112332740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128859752-A-G

112332741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128859753-T-C

http://identifiers.org/hco/2/GRCh38#112333150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128860119-A-C

112333150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128860119-A-G

112333150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128860119-A-T

112333502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128860486-C-T

112333684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128860642-A-G

112333780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128860729-G-T

112334210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128860941-G-A

112334210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128860941-G-T

112334428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128861153-T-C

112334543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128861231-G-A

112334743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862011-G-A

112335283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862302-G-T

112335438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862449-G-T

112335636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862653-G-T

112335654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862670-C-G

112335758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862759-C-T

112335777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862778-G-A

112335885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862882-T-A

112335924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128862917-T-C

112336049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128863040-A-G

112339522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864014-A-T

http://identifiers.org/hco/2/GRCh38#112339544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128864036-C-A

112339544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864036-C-T

112339720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864177-C-G

112339720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864177-C-T

112339888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864336-G-T

112339900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864348-T-C

112339909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864357-C-G

112340004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864460-A-T

112340029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864485-G-C

112340033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24762
most severe consequence: 3 prime UTR variant
orthologous variants: 128864489-G-A