46374354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103843345-C-T

46381498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103841584-G-A

46393266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

46393331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

46398951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828859-T-C

46398951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828859-T-G

46399599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103827432-T-A

46400719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103826536-G-T

46400726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103826529-G-C

http://identifiers.org/hco/17/GRCh38#46400961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103826283-A-C

46400974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103826270-T-C

46400992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103826253-C-T

46401287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825503-T-C

46401289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825501-T-C

46401298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825492-C-G

46401405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825389-A-G

46401431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825363-G-T

46405772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103822738-T-G

46405804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103822712-A-G

46405825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103822689-T-C

46405919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103822396-T-G

46405922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103822385-T-G

46406305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103821948-T-C

46407043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103821270-G-C

46407138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103821170-G-A

46408342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103820590-T-A

46408426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103820511-T-C

http://identifiers.org/hco/17/GRCh38#46408618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103820080-C-A

46408618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103820080-C-T

46408714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819975-T-G

46408957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819729-T-A

46408972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819715-T-A

http://identifiers.org/hco/17/GRCh38#46409014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103819686-A-C

46409014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819686-A-G

46409053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103819648-T-C

46409179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819530-G-A

46409179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819530-G-T

46409209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819508-G-A

46409209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819508-G-C

46409209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819508-G-T

46409243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819474-G-A

46409243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819474-G-T

46409249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819468-T-A

46409322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819386-G-T

http://identifiers.org/hco/17/GRCh38#46409325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103819382-C-A

46409325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819382-C-T

46409327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819380-C-T

46409358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819348-A-G

46409797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818555-G-A

46409821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818534-G-A

46409885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818479-C-G

46409893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818471-G-A

46412245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817457-G-T

46412424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817340-T-C

46412428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817337-T-A

46412430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817335-C-T

46412446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817320-G-A

http://identifiers.org/hco/17/GRCh38#46412447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103817319-C-A

46412448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817318-C-T

46412563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817247-C-T

46412564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817246-A-G

46412679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817160-A-G

http://identifiers.org/hco/17/GRCh38#46412785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103817056-A-C

46412785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817056-A-T

46412806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817033-A-G

46412889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816945-C-T

46412891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816943-C-T

46413001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816854-C-G

46413001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816854-C-T

46414121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103812393-T-C

46414396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103812140-T-G

46414496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103812046-T-C

46414589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103811954-T-C

46414688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103811744-A-G

46414888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103811557-G-A

http://identifiers.org/hco/17/GRCh38#46416711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103810967-C-A

46417793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808845-A-T

46417993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808703-G-A

46418136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808596-G-A

http://identifiers.org/hco/17/GRCh38#46418398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103808419-C-A

46418439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808378-G-T

46418735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808083-G-T

46418862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808062-A-G

46418932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808037-G-A

46418958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808011-G-A

46422357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804837-T-G

46422382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804811-T-C

46422432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804774-T-C

46422432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804774-T-G

http://identifiers.org/hco/17/GRCh38#46423054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103804227-C-A

46423069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103804212-G-T

46424242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802529-G-T

46424609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802145-G-A

46424609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802145-G-T

46424972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103801916-T-C

http://identifiers.org/hco/17/GRCh38#46425248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103801693-A-C

46428471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103798891-G-C

46428729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103798602-C-T

46429239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103798163-G-A

46430664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103796831-A-T

46431186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103796137-T-A

http://identifiers.org/hco/17/GRCh38#46431404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103795858-A-C

46432048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103795047-C-T

46437288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789864-T-C

46437388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789650-G-A

http://identifiers.org/hco/17/GRCh38#46437402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103789635-C-A

http://identifiers.org/hco/17/GRCh38#46437411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103789582-C-A

46437411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789582-C-T

46437505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789488-G-C

46437648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789361-A-G

46437649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789360-T-C

46437651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789358-C-T

46437711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789298-G-C

46437715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789294-T-G

46438085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789104-G-T

46438102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789087-G-A

46438228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788959-G-A

46438239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788948-A-G

http://identifiers.org/hco/17/GRCh38#46438351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103788836-A-C

46438635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788345-G-T

46439059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787939-G-A

http://identifiers.org/hco/17/GRCh38#46439567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103787454-A-C

46439567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787454-A-G

46439579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787442-C-T

46441887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786262-A-G

http://identifiers.org/hco/17/GRCh38#46442307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103785857-C-A

46442307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785857-C-G

46442307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785857-C-T

46444929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784888-T-C

46445041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784764-A-G

http://identifiers.org/hco/17/GRCh38#46445043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103784762-C-A

46445315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784525-A-G

46446075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103783809-G-T

http://identifiers.org/hco/17/GRCh38#46446223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103783662-C-A

46447804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103782458-C-T

46447974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103782272-C-T

46448291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781976-A-G

46448322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781946-G-A

46448329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781939-C-T

46448350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781918-T-C

http://identifiers.org/hco/17/GRCh38#46448351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103781917-C-A

46448351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781917-C-T

46448404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781873-G-T

46448508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781839-T-C

46448508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781839-T-G

46449140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781662-A-G

46449206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781615-C-T

46449605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781179-T-C

46449641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103780996-G-A

http://identifiers.org/hco/17/GRCh38#46449755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103780812-C-A

46449755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103780812-C-T

46450288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103779031-G-A

http://identifiers.org/hco/17/GRCh38#46450315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103779013-C-A

46451340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777935-G-C

46451386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777914-C-T

46454078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103776511-A-G

46454163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103776421-G-A

46454286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103776287-G-T

http://identifiers.org/hco/17/GRCh38#46454339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103776216-C-A

46454507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103776020-T-A

46455369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103775013-G-C

46456444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103774048-T-C

46456484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103774015-C-T

46467457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103771288-G-C

46467638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103769941-C-T

46467765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103769840-T-C

46467984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103769625-A-G

46472921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103767462-A-T

46473099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103767268-G-A

46473969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764718-C-T

http://identifiers.org/hco/17/GRCh38#46475063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103764284-C-A

46475063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764284-C-T

46475064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764283-A-G

http://identifiers.org/hco/17/GRCh38#46475065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103764282-C-A

http://identifiers.org/hco/17/GRCh38#46475136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103764199-C-A

46475136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764199-C-G

46475136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764199-C-T

http://identifiers.org/hco/17/GRCh38#46475155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103764179-A-C

46475155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764179-A-G

46475155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764179-A-T

46475156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103764178-G-T

46475326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103764008-A-T

http://identifiers.org/hco/17/GRCh38#46475825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103763812-A-C

46475891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763753-T-C

46475947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763715-G-T

46476004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763665-G-T

46476053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763581-G-T

46476173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103763460-G-A

46476264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763387-G-A

http://identifiers.org/hco/17/GRCh38#46476305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103763383-A-C

http://identifiers.org/hco/17/GRCh38#46476653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#103763256-C-A

46476653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763256-C-T

46476663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763246-A-G

46476668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763240-A-G

46476668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763240-A-T

46476738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763198-A-G

46476760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103763182-T-C

http://identifiers.org/hco/17/GRCh38#46476882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#103763060-A-C

46476918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103763024-G-C

46476951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103762991-C-T

46476982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103762962-A-T

46477004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103762931-T-G

46477096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103762795-A-G

46477177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103762734-T-A

46486057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103755407-T-A

46486498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103755006-C-G

46486498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103755006-C-T

46486686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103754635-C-G

46486813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31405
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103754346-T-C