2846975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617967-C-T

2847219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71617823-G-A

2847219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71617823-G-C

2847219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71617823-G-T

http://identifiers.org/hco/18/GRCh38#2847365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71617649-C-A

2847365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617649-C-G

2847365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617649-C-T

2847412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617602-G-A

2847412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617602-G-T

2847425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617589-G-A

2847425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617589-G-T

2847457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617558-T-G

2847672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617374-G-A

2847672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617374-G-C

2847675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617371-A-T

http://identifiers.org/hco/18/GRCh38#2847705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71617347-C-A

2847705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617347-C-G

2847705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617347-C-T

http://identifiers.org/hco/18/GRCh38#2847734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71617328-C-A

2847734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617328-C-G

2847734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71617328-C-T

2847822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71617251-T-C

2847852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: 71617221-G-A

2847852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: 71617221-G-T

http://identifiers.org/hco/18/GRCh38#2847972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71617120-C-A

2847972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71617120-C-T

2848109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71617010-A-G

http://identifiers.org/hco/18/GRCh38#2848545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71616576-C-A

2849057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71616059-A-G

2849085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71616031-A-G

2853860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71614127-A-G

2854081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71613919-G-C

2854117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71613893-A-G

2854220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71613799-G-A

2854220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71613799-G-C

2854277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71610740-T-G

2854462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71610557-A-T

http://identifiers.org/hco/18/GRCh38#2855541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71609596-C-A

2855851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71609236-T-C

2856011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71609125-G-A

http://identifiers.org/hco/18/GRCh38#2856087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71609087-A-C

2856745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71608422-C-T

2857102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71608191-C-T

2857543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71607593-A-G

2857608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71607531-T-G

2857751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71607187-G-A

2871427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71600198-A-G

2871763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71599573-T-C

2874228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71598908-G-A

2874228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71598908-G-T

http://identifiers.org/hco/18/GRCh38#2874300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71598827-C-A

2874338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71598790-C-T

2874855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597781-C-T

2875044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597612-G-C

2875050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597606-G-T

2875147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597540-G-A

2875158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597529-G-A

2875158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597529-G-T

2875162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71597525-T-C

2875511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596836-T-G

2875691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596692-C-T

2876380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596360-C-T

2876385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596355-G-A

2876888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596169-G-A

2876929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596127-A-G

2876997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71596061-T-C

2877173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71595934-T-C

2877185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71595922-T-C

2877248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71595864-A-G

2877339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71595620-T-G

2880807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592944-G-A

2881045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592696-T-G

http://identifiers.org/hco/18/GRCh38#2881138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71592590-C-A

2881138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592590-C-G

2881144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592584-C-T

2881243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592480-G-A

2881245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592478-A-G

2881458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592300-G-C

2881458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592300-G-T

2881604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592153-G-A

2881605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71592152-G-T

2881911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71591894-G-A

2883841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71589703-G-A

2883842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71589702-T-C

2883926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71589640-G-A

2884937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71587869-G-A

2884983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: 71587823-C-G

2885077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: 71587729-A-G

http://identifiers.org/hco/18/GRCh38#2885101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71587705-C-A

2885101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: missense variant
orthologous variants: 71587705-C-T

2885201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71587599-C-G

2885218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71587582-T-C

http://identifiers.org/hco/18/GRCh38#2885220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71587580-C-A

2885257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71587572-T-C

2889693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583154-T-C

2889702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583145-T-C

2889734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583116-A-T

2889805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583020-G-A

2889805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583020-G-C

2889813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583012-C-T

2889821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71583003-C-G

2889942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582856-C-G

2889947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582851-T-C

2889947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582851-T-G

2889954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582844-A-G

2890042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582766-A-G

2890067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582739-A-G

2890072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582734-A-G

2890179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582621-G-A

2890266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582543-T-C

2890307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582500-G-T

2890419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582402-A-T

http://identifiers.org/hco/18/GRCh38#2890436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71582386-C-A

2890439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582383-T-C

2890439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582383-T-G

http://identifiers.org/hco/18/GRCh38#2890451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71582378-C-A

2890451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582378-C-G

2890451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582378-C-T

2890466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582363-T-C

2890469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582360-A-G

2890521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71582321-A-G

2890600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582241-T-G

2890630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, stop_gained
orthologous variants: 71582211-G-A

2890630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582211-G-C

2890630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582211-G-T

2890631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, stop_gained
orthologous variants: 71582210-G-A

2890631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582210-G-C

2890698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582143-G-A

2890698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582143-G-C

2890698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71582143-G-T

2890844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71581991-T-C

2890852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581983-A-G

2890872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581963-C-T

2890883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71581952-C-T

2890956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581879-A-T

2890959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581876-G-A

2891041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581794-C-T

2891091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581744-A-T

2891299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581536-C-T

2891301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581534-G-C

2891334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581501-G-A

2891340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581495-A-G

2891454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581381-G-A

2891455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581380-A-G

2891520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581315-G-A

2891652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581186-A-G

2891704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581137-G-A

2891704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581137-G-T

2891748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71581093-C-T

http://identifiers.org/hco/18/GRCh38#2891837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71581013-C-A

http://identifiers.org/hco/18/GRCh38#2891868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71580985-C-A

2891868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71580985-C-T

2891874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71580979-T-A

2891874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71580979-T-C

2891881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71580972-C-T

2892006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71580847-A-G

2892113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71580740-C-G

2892113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 71580740-C-T

2892375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant
orthologous variants: 71580478-T-A

2892668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71580253-G-T

2892679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71580242-A-G

2893162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71579465-C-T

2893867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71576092-A-G

2894209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575848-G-A

2894343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575709-G-C

2894699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575381-G-A

2894720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575360-T-C

2894807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575279-G-A

2894907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575201-C-T

2894940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71575161-G-A

2895218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574926-G-T

2895368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574767-G-C

2895403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574714-G-T

2895493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574643-C-T

http://identifiers.org/hco/18/GRCh38#2895623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71574521-C-A

2895632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574512-T-C

2895775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71574375-T-G

2898438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71572012-C-T

2898439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71572011-G-A

2898528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71571943-A-G

2898634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571843-A-T

2898682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571800-C-T

2898974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571516-G-A

2898974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571516-G-T

2899136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571049-A-T

2899143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71571045-A-G

2899292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570914-G-A

2899317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570890-C-T

2899370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570834-C-T

2899471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570717-T-C

http://identifiers.org/hco/18/GRCh38#2899510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71570679-A-C

2899565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570604-C-G

2899901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570599-T-C

2899988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570515-T-C

2900002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71570502-C-T

2901129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71567858-T-C

2901129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71567858-T-G

2901177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71567804-T-G

2901191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71567785-C-T

2901294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71567701-A-G

2905951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71564485-G-A

2905988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564455-G-A

2906077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564377-G-A

2906077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564377-G-C

2906077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564377-G-T

2906078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564376-G-A

2906078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564376-G-T

2906127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron variant
orthologous variants: 71564345-C-T

2906140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, undefined
orthologous variants: 71564332-C-T

2906227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71564229-C-T

http://identifiers.org/hco/18/GRCh38#2906314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71564150-C-A

2906314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71564150-C-T

2906363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71564098-G-A

2906363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71564098-G-C

2906408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71564052-G-A

2906462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71564004-T-C

http://identifiers.org/hco/18/GRCh38#2906493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563978-A-C

2906493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563978-A-G

http://identifiers.org/hco/18/GRCh38#2906502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563969-C-A

2906502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563969-C-T

2906508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563964-G-A

2906508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563964-G-C

2906508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563964-G-T

2906509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563963-T-A

2906509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563963-T-C

2906509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71563963-T-G

2906526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 71563948-G-T

2906568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71563903-C-G

2906568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71563903-C-T

2906592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563881-C-T

2906678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563770-T-C

http://identifiers.org/hco/18/GRCh38#2906687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563761-C-A

2906687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563761-C-T

2906710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563741-G-A

2906710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563741-G-T

2906748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563710-A-G

http://identifiers.org/hco/18/GRCh38#2906765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563696-C-A

2906765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563696-C-G

2906765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563696-C-T

http://identifiers.org/hco/18/GRCh38#2906815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563641-C-A

2906815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563641-C-T

2906818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563616-A-G

2906818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 71563616-A-T

http://identifiers.org/hco/18/GRCh38#2906827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563607-C-A

2906827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563607-C-G

2906827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71563607-C-T

2906889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71563543-A-G

2906950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563452-G-A

2906950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563452-G-C

2906950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563452-G-T

2906965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71563437-A-G

http://identifiers.org/hco/18/GRCh38#2907180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563238-C-A

2907180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71563238-C-T

2907243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563174-G-T

http://identifiers.org/hco/18/GRCh38#2907263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71563152-C-A

2907263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563152-C-G

2907263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71563152-C-T

2908927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71563018-C-T

2908964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562984-T-C

2908964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562984-T-G

2908983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71562965-T-G

2908989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71562959-G-A

2908989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71562959-G-C

2909092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71562872-A-T

2909458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71562506-C-T

http://identifiers.org/hco/18/GRCh38#2909648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71562279-A-C

2909702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562229-C-G

2909702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562229-C-T

2909792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562139-G-A

2909792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71562139-G-T

2910687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71561419-C-T

2910694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71561412-A-T

2910695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71561411-G-C

2910728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71561378-T-G

2913011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71560141-A-G

2913019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71560133-G-A

http://identifiers.org/hco/18/GRCh38#2913033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71560119-C-A

2913033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71560119-C-T

http://identifiers.org/hco/18/GRCh38#2913303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559850-A-C

2913303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71559850-A-G

http://identifiers.org/hco/18/GRCh38#2913389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559764-C-A

2913467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559698-T-G

http://identifiers.org/hco/18/GRCh38#2913524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559634-A-C

http://identifiers.org/hco/18/GRCh38#2913560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559619-C-A

2913560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559619-C-T

http://identifiers.org/hco/18/GRCh38#2913563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559616-C-A

2913563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559616-C-G

2913563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559616-C-T

http://identifiers.org/hco/18/GRCh38#2913575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559605-C-A

2913575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559605-C-T

2913583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559598-A-G

http://identifiers.org/hco/18/GRCh38#2913646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559558-C-A

2913646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559558-C-T

http://identifiers.org/hco/18/GRCh38#2913656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559530-C-A

2913656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559530-C-T

2913678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559495-G-T

2913680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559493-G-T

http://identifiers.org/hco/18/GRCh38#2913683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559490-C-A

2913683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559490-C-T

2913693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559480-G-T

2913796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559424-G-T

2913821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559400-A-G

http://identifiers.org/hco/18/GRCh38#2913918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559312-C-A

2913918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71559312-C-T

2914098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71559145-G-A

http://identifiers.org/hco/18/GRCh38#2914106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71559137-C-A

2914162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71559067-G-A

2914234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71559001-A-G

2914314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558920-G-A

2914359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558879-G-C

2914440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558791-G-T

2914445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558786-T-C

http://identifiers.org/hco/18/GRCh38#2914463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558765-C-A

2914473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558755-G-A

2914473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558755-G-T

http://identifiers.org/hco/18/GRCh38#2914474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558754-C-A

2914538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558707-G-T

2914543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558706-T-C

2914569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558680-A-G

2914584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558667-T-C

http://identifiers.org/hco/18/GRCh38#2914600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558648-C-A

2914869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558481-G-T

http://identifiers.org/hco/18/GRCh38#2914946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558419-C-A

2914946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558419-C-G

2914984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558384-G-A

2914984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558384-G-T

2915013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558355-G-T

2915019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558349-G-A

2915020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558348-C-T

2915098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558270-T-C

2915116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558253-G-A

http://identifiers.org/hco/18/GRCh38#2915167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558208-C-A

2915167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558208-C-G

2915167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558208-C-T

2915254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558123-G-C

2915254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558123-G-T

2915260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558117-A-G

http://identifiers.org/hco/18/GRCh38#2915287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71558089-C-A

2915287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558089-C-T

2915374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558002-T-C

2915374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71558002-T-G

2915401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557979-G-T

http://identifiers.org/hco/18/GRCh38#2915427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71557948-A-C

2915427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557948-A-G

2915507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557870-A-G

http://identifiers.org/hco/18/GRCh38#2915615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71557840-C-A

2915615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557840-C-G

2915615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557840-C-T

2915806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557789-A-G

2915889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557706-G-C

2915889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 71557706-G-T

http://identifiers.org/hco/18/GRCh38#2915943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19881
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71557663-C-A