http://identifiers.org/hco/8/GRCh38#94641261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386493-A-C

94641261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: 11386493-A-G

94641261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: 11386493-A-T

94641312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: 11386441-T-A

94641312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: 11386441-T-C

94641312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 5 prime UTR variant
orthologous variants: 11386441-T-G

http://identifiers.org/hco/8/GRCh38#94641373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386380-A-C

94641626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386095-T-A

http://identifiers.org/hco/8/GRCh38#94641633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386088-C-A

94641633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386088-C-G

94641633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386088-C-T

http://identifiers.org/hco/8/GRCh38#94641638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386083-C-A

94641644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386077-T-C

http://identifiers.org/hco/8/GRCh38#94641650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386071-A-C

94641650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386071-A-G

94641650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386071-A-T

94641657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386064-T-A

94641657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386064-T-C

http://identifiers.org/hco/8/GRCh38#94641679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11386039-C-A

94641679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11386039-C-T

http://identifiers.org/hco/8/GRCh38#94641732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11385989-C-A

94641732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11385989-C-G

94641820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11385910-G-A

94641820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11385910-G-T

http://identifiers.org/hco/8/GRCh38#94641886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11385848-C-A

94641886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11385848-C-T

94642097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11385628-G-C

94642234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11385476-G-T

94642419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11385325-C-T

http://identifiers.org/hco/8/GRCh38#94642481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#11385260-C-A

94642604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11385139-T-C

94642907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384818-C-T

94643109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384650-G-A

94643171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384588-G-A

94643171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384588-G-T

94643216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384548-T-C

94643216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384548-T-G

http://identifiers.org/hco/8/GRCh38#94643480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11384274-A-C

94643506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384233-G-A

94643551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384185-T-G

http://identifiers.org/hco/8/GRCh38#94643554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11384182-C-A

94643554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384182-C-T

94643676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11384008-T-C

94643776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11383916-G-A

94643913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11383795-T-C

94644211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11383434-A-G

94644368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11383287-G-T

94644679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11382582-G-A

94645842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379864-A-G

94645917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379644-A-G

94646048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379528-T-A

94646048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379528-T-C

94646048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379528-T-G

94646097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379473-G-A

94646097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379473-G-T

http://identifiers.org/hco/8/GRCh38#94646118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11379452-C-A

94646123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11379448-A-G

http://identifiers.org/hco/8/GRCh38#94646173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#11379398-A-C

94646216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11379355-G-A

94646243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11379328-C-T

94646888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11378165-T-C

http://identifiers.org/hco/8/GRCh38#94648361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11377278-C-A

94648361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11377278-C-T

94653743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11373020-T-A

94653743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11373020-T-C

94653818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11372948-A-T

94654611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11372150-A-T

94656654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11371365-A-G

94656834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11371177-A-G

94657095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11370975-C-T

94657161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11370910-G-A

94657620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11370440-C-T

http://identifiers.org/hco/8/GRCh38#94661825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11367567-C-A

94661827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367565-G-T

94661828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367564-T-G

94661880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367540-G-A

94662129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367299-G-T

94662147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367281-T-C

94662149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367279-A-T

94662159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367269-A-G

94662207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11367247-T-G

94662288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11367165-G-T

94662378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 11367075-T-C

94662391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11367062-A-G

http://identifiers.org/hco/8/GRCh38#94662395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11367058-C-A

94662395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11367058-C-T

94662574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366887-T-C

94662574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366887-T-G

94662578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366883-T-C

94662579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366882-T-C

94663065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366735-G-A

94663645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11366334-T-C

94664550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11365595-G-C

94664550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11365595-G-T

http://identifiers.org/hco/8/GRCh38#94664565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11365580-A-C

94664565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11365580-A-G

94665109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11365091-T-C

94665288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364935-G-A

94665288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364935-G-T

94665346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364881-G-A

94665346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364881-G-T

http://identifiers.org/hco/8/GRCh38#94665457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11364768-A-C

94667698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361995-G-A

94667698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361995-G-T

94667914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361288-T-A

94668101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11361101-G-A

94668101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11361101-G-C

94668286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11360918-T-G

94671220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11360432-G-A

94671355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11360080-T-C

94671540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: missense variant
orthologous variants: 11359867-A-G

94671618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: missense variant
orthologous variants: 11359789-G-C

http://identifiers.org/hco/8/GRCh38#94671712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11359698-C-A

94671712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11359698-C-T

94671716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11359694-A-G

94671861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11359676-T-C

94671909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11359637-C-T

http://identifiers.org/hco/8/GRCh38#94672937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11358964-C-A

94672937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11358964-C-T

94672976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11358930-G-A

94674160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357811-G-A

94674160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357811-G-C

94674160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357811-G-T

94674563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357401-G-A

94674606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357359-G-A

94674606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357359-G-C

94674606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357359-G-T

94674941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11357005-A-T

94675212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11356728-G-A

94675407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11356613-T-C

94675496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11356530-T-C

94676917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11354903-C-T

94676925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11354895-G-A

http://identifiers.org/hco/8/GRCh38#94676957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11354873-A-C

94677123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11354730-T-G

94677504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11354103-C-T

94677746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353884-C-T

94677777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353854-G-A

94677777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353854-G-C

http://identifiers.org/hco/8/GRCh38#94678160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11353504-C-A

94678271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: stop gained
orthologous variants: 11353393-C-T

94678395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353272-A-G

94678401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353266-G-T

94678463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353204-A-G

http://identifiers.org/hco/8/GRCh38#94678507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11353161-C-A

94678547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353127-T-C

94678575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353079-A-G

94678575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353079-A-T

94678592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11353063-T-C

94678669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11352989-G-A

94678695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11352962-A-G

94678830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11352853-T-A

94678961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11352738-G-A

94679188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11352000-A-T

94679192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351996-T-C

94679533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351627-G-A

94679542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351618-C-T

94679587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351568-A-G

94679592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351563-C-T

94679603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11351555-G-C

94684354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11350699-C-T

94684358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11350695-G-A

94684484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11350588-G-T

http://identifiers.org/hco/8/GRCh38#94684498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11350574-C-A

94684498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11350574-C-T

http://identifiers.org/hco/8/GRCh38#94684539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11350534-A-C

94690692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11346440-G-A

94690798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11346336-C-T

94690800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11346335-T-C

94690864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11346271-G-A

94691123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11345714-A-G

94691942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344938-C-T

94692119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344765-T-C

94692303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344620-T-C

94692310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344613-G-A

94692583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344346-G-T

94692608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344330-T-C

94692609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344329-A-G

http://identifiers.org/hco/8/GRCh38#94692850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11344087-A-C

94692875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344062-T-C

94692914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11344023-T-C

94692940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11343997-G-A

94692942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11343995-T-C

94693035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11343944-T-C

http://identifiers.org/hco/8/GRCh38#94693403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11342687-C-A

94693710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11342427-A-G

94693741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11342397-G-A

94693891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11342281-A-G

94694275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11341594-T-A

94694454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11341471-A-G

94694782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11341256-G-C

94694902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11340994-T-C

94695098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11340804-A-G

94695943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11339851-G-A

94695961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11339833-G-A

94696236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11339595-G-A

94696238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11339593-C-T

94696620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11339040-T-C

94696730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11338947-G-C

94696808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11338873-G-A

94696808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11338873-G-C

94696873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 11338808-A-G

94696873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, missense_variant
orthologous variants: 11338808-A-T

http://identifiers.org/hco/8/GRCh38#94696880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11338801-C-A

94696880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron_variant, missense_variant, stop_gained
orthologous variants: 11338801-C-T

94696942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11338739-G-A

94696942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_lost
orthologous variants: 11338739-G-T

94696944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11338737-A-T

http://identifiers.org/hco/8/GRCh38#94697058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11338654-C-A

94698554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11337975-C-T

94698579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11337958-T-C

http://identifiers.org/hco/8/GRCh38#94698772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11337796-A-C

94698949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11337653-G-A

94699003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: intron variant
orthologous variants: 11337595-C-T

94705986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333412-A-G

94705986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333412-A-T

94705989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333409-G-A

94705989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333409-G-C

94705989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333409-G-T

94706000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333398-T-A

94706000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333398-T-C

94706030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333368-T-A

94706030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333368-T-C

http://identifiers.org/hco/8/GRCh38#94706048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11333351-C-A

94706048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333351-C-G

94706075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333324-A-G

94706082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333319-G-A

94706082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333319-G-T

94706163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333249-A-T

http://identifiers.org/hco/8/GRCh38#94706205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11333211-A-C

94706205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333211-A-G

http://identifiers.org/hco/8/GRCh38#94706272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11333145-C-A

94706287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333132-T-C

94706289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333130-A-G

94706289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333130-A-T

94706307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333115-T-C

94706307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333115-T-G

94706311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333111-T-A

94706311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333111-T-C

94706311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333111-T-G

http://identifiers.org/hco/8/GRCh38#94706315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11333107-C-A

94706315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333107-C-G

94706315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333107-C-T

94706370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11333058-A-G

94706456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332956-T-C

94706559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332768-T-A

94706860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332483-T-C

94706942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332414-A-G

94706965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332395-A-G

94707288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332104-A-G

94707296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332096-A-G

94707360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332036-G-A

94707360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11332036-G-T

http://identifiers.org/hco/8/GRCh38#94707361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25966
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#11332035-C-A