35382176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-A

35382176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-T

35382202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-A

35382202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-T

35382245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-A

35382245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-T

35382249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445816-T-A

35382249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445816-T-C

35382282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-G

35382289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-A-G

35382324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-A

35382324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-T

35382339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-A-G

35382339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-A-T

http://identifiers.org/hco/19/GRCh38#35382341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445908-C-A

35382341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-C-T

35382343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-C

35382351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-T

35382354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-C

35382354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-G

35382364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-T

35382371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-A

35382371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-T

35382375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445942-A-G

35382376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-T-A

35382376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-T-C

http://identifiers.org/hco/19/GRCh38#35382387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445954-C-A

35382387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445954-C-T

35382389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-A

35382389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-C

35382389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-G

35382393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445960-T-C

35382400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-T-C

35382423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-C

35382435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-T-A

35382435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-T-C

http://identifiers.org/hco/19/GRCh38#35382949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446014-C-A

35382949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40446014-C-T

35382957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446022-A-G

35382957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446022-A-T

35382958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-G

35382958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-T

35382962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-T

http://identifiers.org/hco/19/GRCh38#35382967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446032-C-A

35382967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446032-C-T

35382968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-G

35382968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-T

http://identifiers.org/hco/19/GRCh38#35382970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446035-C-A

35382978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-A

35382978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-C

35382988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-A

35382988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-T

35382994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446059-T-C

http://identifiers.org/hco/19/GRCh38#35382995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

35382995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446060-C-G

http://identifiers.org/hco/19/GRCh38#35382996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446061-A-C

35382996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-G

35382996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-T

35382998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-A

35382998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-C

35382998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-T

http://identifiers.org/hco/19/GRCh38#35383012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446077-C-A

35383012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446077-C-T

35383015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-A

35383015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-T

35383019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-A

35383019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-T

35383021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446086-T-C

35383037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-A

35383043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-G-A

http://identifiers.org/hco/19/GRCh38#35383057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446122-C-A

35383057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446122-C-T

http://identifiers.org/hco/19/GRCh38#35383063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446128-C-A

35383063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-C-G

35383063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-C-T

35383064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-T-A

35383064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-T-C

35383065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-A

35383065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-T

35383074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-G-A

35383074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-G-T

35383075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-A-G

35383076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-A

35383076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-T

35383100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446165-T-A

35383100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446165-T-C

35383111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-A-T

35383114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446179-A-G

35383117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-G

35383117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-T

http://identifiers.org/hco/19/GRCh38#35383122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446187-C-A

35383122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446187-C-T

35383123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446188-T-C

http://identifiers.org/hco/19/GRCh38#35383156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446221-C-A

35383156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446221-C-T

http://identifiers.org/hco/19/GRCh38#35383162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446227-C-A

35383174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-C

http://identifiers.org/hco/19/GRCh38#35383183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446248-C-A

35383183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-C-G

35383183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-C-T

35383184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-A-G

35383184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-A-T

35383200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446266-C-G

35383200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446266-C-T

35383249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446315-A-G

35383285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-A-G

35383293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446359-C-T

35383296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-C

35383296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-T

35383308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-C

35383308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-T

http://identifiers.org/hco/19/GRCh38#35383324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446390-C-A

35383324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-C-T

35383329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-A

35383329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-C

35383337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-A-G

35383347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-A-G

35383347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-A-T

35383352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-T-A

35383352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-T-C

http://identifiers.org/hco/19/GRCh38#35383354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446420-C-A

35383356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-A

35383356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-T

35383358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-C

35383358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-G

35383365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-T-C

http://identifiers.org/hco/19/GRCh38#35383366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446432-C-A

35383366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-C-T

http://identifiers.org/hco/19/GRCh38#35383371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446437-C-A

35383371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-T

35383372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-A

35383378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-T

http://identifiers.org/hco/19/GRCh38#35383390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446456-C-A

35383390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-C-T

http://identifiers.org/hco/19/GRCh38#35383393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446459-C-A

35383393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446459-C-G

35383420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-T

http://identifiers.org/hco/19/GRCh38#35383452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446525-C-A

35383452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446525-C-T

http://identifiers.org/hco/19/GRCh38#35383460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446533-C-A

35383460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446533-C-T

35383473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-A

35383473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-T

http://identifiers.org/hco/19/GRCh38#35383485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446558-C-A

35383485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446558-C-T

http://identifiers.org/hco/19/GRCh38#35383514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

35383514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446587-C-G

35383547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-G-A

35383564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446637-G-A

35383566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446639-G-A

http://identifiers.org/hco/19/GRCh38#35383603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446676-A-C

http://identifiers.org/hco/19/GRCh38#35383612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446685-C-A

35383612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-G

35383613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-T-C

35383613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-T-G

35383617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446690-A-G

35383636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446709-A-G

http://identifiers.org/hco/19/GRCh38#35383734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446806-C-A

35383734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-C-G

35383752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-T-C

35383764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-T-C

35383802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-C

35383817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-A

35383817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-T

35383848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446921-G-A

35383848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446921-G-T

35383857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446930-T-C

35383864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-A

35383864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-C

35383864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-T

35383876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446949-A-G

35383881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446954-T-C

35383898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-A

35383898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-T

35383905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-A

35383905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-C

35383905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-T

35383914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446987-A-G

35383915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-T

35383920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446993-T-A

http://identifiers.org/hco/19/GRCh38#35383925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446998-C-A

35383925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-C-T

35383927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447000-C-T

35383929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-G-T

http://identifiers.org/hco/19/GRCh38#35383935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447008-C-A

35383935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447008-C-T

35383946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447019-G-A

35383946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447019-G-T

35383956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447029-A-G

http://identifiers.org/hco/19/GRCh38#35383957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447030-C-A

35383957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-C-G

35383957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-C-T

35383959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-A

35383959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-C

http://identifiers.org/hco/19/GRCh38#35383960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447033-A-C

35383960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-A-G

http://identifiers.org/hco/19/GRCh38#35383961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447034-C-A

35383961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-G

35383961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-T

35383982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447055-A-G

35383986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-G

35383999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-A

35383999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-T

35384002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-A

35384002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-C

35384002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-T

http://identifiers.org/hco/19/GRCh38#35384009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447082-C-A

35384009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447082-C-T

35384012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-A

http://identifiers.org/hco/19/GRCh38#35384021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447094-C-A

35384021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-G

35384021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-T

35384023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-G

35384023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-T

http://identifiers.org/hco/19/GRCh38#35384024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447097-A-C

35384024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-G

35384024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3202
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-T