101089347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094661-T-C

http://identifiers.org/hco/10/GRCh38#101089450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45094802-C-A

101089450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094802-C-T

http://identifiers.org/hco/10/GRCh38#101089454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45094806-C-A

101089474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094825-A-G

101089479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094830-G-A

101089479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094830-G-T

101089509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094855-G-A

101089509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094855-G-T

http://identifiers.org/hco/10/GRCh38#101089522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45094866-C-A

http://identifiers.org/hco/10/GRCh38#101089523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45094867-A-C

http://identifiers.org/hco/10/GRCh38#101089527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45094871-C-A

101089527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094871-C-T

101089578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094908-G-C

101089578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094908-G-T

101089626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094942-G-A

101089666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094982-A-G

101089681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094997-T-C

101089681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094997-T-G

101089682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45094998-A-G

101089698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095015-A-G

http://identifiers.org/hco/10/GRCh38#101089748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45095065-C-A

101089835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095150-G-A

101089901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095219-G-T

http://identifiers.org/hco/10/GRCh38#101089903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45095221-C-A

101089995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095312-T-A

101089995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095312-T-C

http://identifiers.org/hco/10/GRCh38#101090028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45095346-C-A

101090028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095346-C-T

101090075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095394-A-G

http://identifiers.org/hco/10/GRCh38#101090124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45095442-C-A

101090124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095442-C-G

101090127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095445-G-T

101090183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095499-T-G

101090226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45095540-G-A

http://identifiers.org/hco/10/GRCh38#101090781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45098036-C-A

101090781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098036-C-T

http://identifiers.org/hco/10/GRCh38#101090782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45098037-C-A

101090865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098134-G-A

101090971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098235-A-G

101091012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098280-C-T

101091245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098548-G-T

101091540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45098845-G-T

101092013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45099228-G-A

101092031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45099246-G-A

101092065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45099287-A-T

101092167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45099397-C-T

http://identifiers.org/hco/10/GRCh38#101092207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45099432-A-C

101092262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45099495-C-T

101092771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45101937-G-T

101093258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45102524-T-C

101093665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45102940-A-G

101094149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45103324-G-T

101094538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45103738-G-C

101094626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45103823-G-A

101094626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45103823-G-C

101094631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45103828-C-G

http://identifiers.org/hco/10/GRCh38#101095048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45104676-A-C

101095366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45105013-G-C

101095515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45105161-G-A

101095641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45105275-G-A

101095657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45105291-C-T

101095998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45105679-A-T

101096179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45105827-C-T

101096262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45105908-T-G

101097069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45106670-C-T

http://identifiers.org/hco/10/GRCh38#101097194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45106779-C-A

101097630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45107206-T-A

101097780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45107314-T-A

http://identifiers.org/hco/10/GRCh38#101097949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45107717-C-A

101097949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45107717-C-T

101102144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45110984-C-T

101102222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111050-G-A

101102247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111075-A-G

101102264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111086-C-T

101102638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111446-C-T

101102896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111695-G-C

101102981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111747-T-C

http://identifiers.org/hco/10/GRCh38#101103008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45111784-C-A

101103016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111789-A-G

101103017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111790-G-T

101103060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111852-T-C

101103140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45111921-C-T

101103320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45112134-C-T

101103343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45112159-G-A

101103492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45112312-G-A

101103716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45112529-T-C

101104057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45112838-G-C

101106613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114594-A-G

101106631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114612-C-T

101106689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114674-G-A

101106763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114750-G-A

101106763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114750-G-T

101106843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114822-T-C

101106851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45114830-C-G

http://identifiers.org/hco/10/GRCh38#101107100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45115075-C-A

101107100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115075-C-T

101107116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115091-C-T

101107186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115166-C-T

http://identifiers.org/hco/10/GRCh38#101107326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45115361-C-A

101107326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115361-C-T

101107391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115428-G-A

101107518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115515-C-T

101107530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115527-C-T

101107542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115540-G-A

101107543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115541-C-T

101107672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115670-G-A

101107677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115675-C-G

101107899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115887-C-T

101107922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115907-G-A

101107990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45115967-G-A

101108050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116027-C-T

101108233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116194-C-T

101108413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116307-T-A

101108413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116307-T-C

101108481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116336-G-T

101108494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116349-C-T

http://identifiers.org/hco/10/GRCh38#101108499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45116354-C-A

101108627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116490-C-T

101108672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116547-A-G

101108690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116562-G-A

101108808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45116642-C-T

101110129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45117758-G-A

101110129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45117758-G-T

101110949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45118150-C-T

101111022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45118231-G-A

101111177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45118335-G-T

101111272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45118428-G-A

http://identifiers.org/hco/10/GRCh38#101111431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45118574-A-C

101111481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45118622-C-G

101112941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45120345-T-A

101112941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45120345-T-C

101113133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45120532-G-A

101113220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120615-C-T

101113290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120685-C-T

101113313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120708-G-A

101113313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120708-G-T

101113365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120759-T-C

http://identifiers.org/hco/10/GRCh38#101113394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45120807-C-A

101113394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45120807-C-T

101113412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45120825-C-T

101113447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120857-G-A

101113508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45120917-G-C

http://identifiers.org/hco/10/GRCh38#101113643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45121000-A-C

101114136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45121135-C-T

101114151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45121150-A-G

101114262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45121248-A-G

101114379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45121352-G-T

101114686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45122218-G-T

101114691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45122223-C-T

http://identifiers.org/hco/10/GRCh38#101114737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45122273-C-A

101114862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45122388-T-C

101114971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45122464-C-T

101115010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45122502-A-G

101115015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45122507-T-C

101115190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45122671-C-G

http://identifiers.org/hco/10/GRCh38#101115312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45122790-C-A

101115312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45122790-C-T

101115453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45122933-G-A

101118773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45127748-G-C

101119051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45128026-T-A

http://identifiers.org/hco/10/GRCh38#101119342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45128366-A-C

101119546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45128577-G-C

101119593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45128622-G-C

http://identifiers.org/hco/10/GRCh38#101119595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45128624-A-C

http://identifiers.org/hco/10/GRCh38#101119742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45128749-C-A

101119742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45128749-C-G

101119910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45128921-C-T

101119939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45128951-T-C

101120849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129433-C-T

101120866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129450-G-A

101120880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129464-G-A

101121106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129654-A-G

101121299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129840-G-C

101121426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129943-G-A

101121432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129952-G-A

101121464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129986-G-A

101121464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45129986-G-C

101121498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130003-C-T

101121511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130016-C-T

101121700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130204-G-A

101121880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130386-G-A

101121886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130392-G-A

101122140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45130647-G-A

http://identifiers.org/hco/10/GRCh38#101122545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45131042-A-C

http://identifiers.org/hco/10/GRCh38#101122901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45131430-C-A

101122901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131430-C-T

101122950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131476-C-T

101122974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131509-T-A

101122978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131520-C-G

101123059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131606-C-T

http://identifiers.org/hco/10/GRCh38#101123109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45131662-C-A

101123109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131662-C-G

101123460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45131989-G-C

101123558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45132087-G-T

101124388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45132982-C-T

101124389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45132983-G-A

101124765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133317-G-T

101124806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133344-G-A

101124821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133365-C-T

101125076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133563-T-C

101125112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133622-T-G

101125126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133625-A-T

101125476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133901-C-G

101125476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133901-C-T

101125479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133906-T-C

101125576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133943-T-A

101125619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45133976-G-T

101125649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134004-T-C

101125701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134068-G-T

101125787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134153-C-T

101125810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134176-G-C

101125813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134179-A-G

http://identifiers.org/hco/10/GRCh38#101125834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45134200-C-A

101125834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134200-C-T

101125899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134272-G-C

101125917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134285-C-G

101125997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134360-C-T

101126037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134397-G-C

101126402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134692-A-G

101126483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134762-G-A

101126502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134781-C-T

101126586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134864-C-T

101126589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134867-A-G

101126593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134871-C-T

101126594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134872-A-G

101126694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134949-C-T

101126702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45134957-T-C

101126881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135105-A-G

101126918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135145-A-G

101126982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45135202-T-C

101127062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: non coding transcript exon variant
orthologous variants: 45135279-T-C

101127199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135421-T-C

101127566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135723-C-T

101127647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135764-A-G

101127831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45135930-G-A

101128044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136210-C-T

101128280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136492-T-C

101128314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136533-T-A

101128314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136533-T-C

101128442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136658-G-A

101128452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136668-C-G

101128537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136749-C-T

101128595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136801-C-T

101128602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136808-G-C

101128661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136856-C-T

101128689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136878-G-A

101128709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136899-G-C

101128738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45136924-C-T

101129637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45137471-T-C

101130366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138256-G-A

101130366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138256-G-T

101130393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138283-G-T

101130564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138378-G-T

http://identifiers.org/hco/10/GRCh38#101130645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45138459-C-A

101130684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138496-G-A

101130684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138496-G-T

101130774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45138585-T-C

101130886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45138696-G-T

http://identifiers.org/hco/10/GRCh38#101131088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45138899-C-A

101131180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138994-C-G

101131180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45138994-C-T

101131185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45139000-T-A

101131185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45139000-T-C

101131185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45139000-T-G

101131320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45139135-G-T