19349249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825280-T-C

19349249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825280-T-G

19350110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825845-A-G

19350110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825845-A-T

19350124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825859-A-G

19350124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825859-A-T

http://identifiers.org/hco/13/GRCh38#19350169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56825897-A-C

19350169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825897-A-G

19350175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825903-T-C

http://identifiers.org/hco/13/GRCh38#19350177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56825905-A-C

19350177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825905-A-G

19350177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825905-A-T

19350203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825931-A-G

19350215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825943-T-C

19350220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825948-G-A

19350220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825948-G-C

19350220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56825948-G-T

http://identifiers.org/hco/13/GRCh38#19350235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56825963-A-C

19350235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825963-A-G

19350235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825963-A-T

19350241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825969-A-G

19350241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825969-A-T

19350269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825986-T-A

19350269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825986-T-C

19350270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-G-A

19350270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-G-C

19350270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-G-T

19350275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825992-T-A

19350289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826006-T-C

19350344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826061-T-A

19350344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826061-T-C

19350344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826061-T-G

19350592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826600-A-G

19350627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826633-G-A

19350737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826736-T-A

19350737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826736-T-C

19351007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826828-T-C

19351116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826907-G-C

19351162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826953-G-A

19351162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826953-G-C

19351257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827269-A-G

19351265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827277-A-G

http://identifiers.org/hco/13/GRCh38#19351316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56827324-C-A

19351316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827324-C-T

19351330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56827338-G-A

19351330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56827338-G-T

19351348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56827347-G-A

19351348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56827347-G-C

19351348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56827347-G-T

19351375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56827374-T-C

19357368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834970-G-T

19357449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56835048-T-C

19357530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56835129-G-A

19357530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56835129-G-T

19357543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56835142-G-A

19357543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56835142-G-T

19357617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835214-T-C

19357625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835222-G-A

19357625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835222-G-T

http://identifiers.org/hco/13/GRCh38#19357631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56835228-C-A

19357631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835228-C-G

19357631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835228-C-T

19357684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835309-G-A

19357684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835309-G-T

19366551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839697-G-A

19366551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839697-G-T

http://identifiers.org/hco/13/GRCh38#19366597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56839743-C-A

19366597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839743-C-T

http://identifiers.org/hco/13/GRCh38#19366614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56839760-C-A

19366614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839760-C-G

19366614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839760-C-T

19366626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839772-G-A

19366626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839772-G-C

19366626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839772-G-T

19366653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839799-G-A

19366653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839799-G-T

19366695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839841-A-G

19366701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56839847-A-G

19366786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840012-G-A

19366786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840012-G-C

19366919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840129-G-A

19366919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840129-G-T

19366992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56840210-T-C

http://identifiers.org/hco/13/GRCh38#19367138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56840356-A-C

19367138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56840356-A-G

19367138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56840356-A-T

19367144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56840362-A-G

19367144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56840362-A-T

19367775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840605-C-G

19369215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844641-G-A

19369229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844654-T-A

http://identifiers.org/hco/13/GRCh38#19369328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56844715-A-C

19369328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844715-A-T

http://identifiers.org/hco/13/GRCh38#19369415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56844760-C-A

19369415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844760-C-T

19369417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844762-G-A

19369417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844762-G-T

19369532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56844876-T-A

19369532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56844876-T-C

19369598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56844942-G-T

19369690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845037-T-A

19369690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845037-T-C

19369690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845037-T-G

19374915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845747-T-A

19374915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845747-T-C

19374915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845747-T-G

19374946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845773-G-A

19374946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845773-G-C

19374946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845773-G-T

19375066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56845901-T-C

http://identifiers.org/hco/13/GRCh38#19375084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56845919-C-A

19375084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56845919-C-T

19375132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845965-A-G

19375132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845965-A-T

http://identifiers.org/hco/13/GRCh38#19375146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56845975-C-A

19375146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845975-C-T

19375147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845976-G-A

19375147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845976-G-C

19375147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845976-G-T

http://identifiers.org/hco/13/GRCh38#19375165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56845990-C-A

19375165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845990-C-T

19375940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847786-G-T

19376019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847855-T-A

http://identifiers.org/hco/13/GRCh38#19376078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56847912-C-A

19376078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847912-C-G

19376131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847964-G-T

19376133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847966-T-C

19376133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847966-T-G

19376143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847976-A-G

19376143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847976-A-T

19376145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847978-T-G

19376163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847996-T-C

19376170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848003-T-C

19376170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848003-T-G

19376171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848004-G-T

http://identifiers.org/hco/13/GRCh38#19376177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848010-A-C

19376177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848010-A-G

19376177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848010-A-T

19376191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848024-G-A

19376191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848024-G-C

19376191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848024-G-T

19376197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848030-T-A

19376197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848030-T-C

19376197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848030-T-G

19376204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848037-A-G

19376204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848037-A-T

19376218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56848211-A-G

19376218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56848211-A-T

19376247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848240-G-A

19376247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848240-G-T

19376254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848247-G-A

19376254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848247-G-T

19376301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848294-T-A

19376301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848294-T-C

19376301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56848294-T-G

http://identifiers.org/hco/13/GRCh38#19376331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848325-C-A

19376331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848325-C-T

http://identifiers.org/hco/13/GRCh38#19376332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848326-A-C

19376332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848326-A-G

19376332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848326-A-T

http://identifiers.org/hco/13/GRCh38#19376335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848329-C-A

19376335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848329-C-G

19376335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848329-C-T

19376379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848358-T-A

19376379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848358-T-C

19376390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848369-G-A

19376390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848369-G-C

19376390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848369-G-T

19376414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-A

19376414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-C

19376414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-T

http://identifiers.org/hco/13/GRCh38#19376449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848590-C-A

19376449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848590-C-T

19378741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863958-T-A

http://identifiers.org/hco/13/GRCh38#19378797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56863988-C-A

19378797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863988-C-G

19378797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863988-C-T

19378836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864027-A-G

19378855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864830-A-G

19378855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864830-A-T

19378917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56864892-T-A

19378917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56864892-T-C

19378926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56864901-A-G

19378926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56864901-A-T

19378981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864964-T-C

19378995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864985-T-C

http://identifiers.org/hco/13/GRCh38#19379027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56865017-C-A

19379027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865017-C-T

19379038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865023-A-G

19379038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865023-A-T

19379042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865027-G-T

http://identifiers.org/hco/13/GRCh38#19379092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56865075-C-A

19379092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865075-C-G

19379118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865095-G-T

19379216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865186-G-T

http://identifiers.org/hco/13/GRCh38#19381146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866497-C-A

19381146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866497-C-T

19381178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56866528-T-C

19381178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56866528-T-G

19381181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56866531-A-G

19381181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56866531-A-T

19381267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56866617-G-T

http://identifiers.org/hco/13/GRCh38#19381270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866620-C-A

19381270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56866620-C-T

http://identifiers.org/hco/13/GRCh38#19381285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866635-C-A

19381285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56866635-C-G

19381285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56866635-C-T

http://identifiers.org/hco/13/GRCh38#19381297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866647-C-A

19381297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56866647-C-T

http://identifiers.org/hco/13/GRCh38#19381387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866736-A-C

19381387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866736-A-G

19381387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866736-A-T

19381412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866750-T-A

19381415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866753-G-A

19381415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866753-G-T

19381437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866775-C-G

19381437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866775-C-T

19381438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866776-C-T

19381455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866794-C-G

19381458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866797-G-A

http://identifiers.org/hco/13/GRCh38#19381583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866900-A-C

19381583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866900-A-G

19381583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866900-A-T

19385949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871644-T-C

http://identifiers.org/hco/13/GRCh38#19385995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56871690-C-A

19385995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871690-C-G

19385995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871690-C-T

19386000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871695-T-A

19386000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871695-T-C

http://identifiers.org/hco/13/GRCh38#19386036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56871731-A-C

19386036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871731-A-G

19386051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871746-T-C

19386051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56871746-T-G

19386111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871803-G-A

19386111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871803-G-T

19386156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871844-G-T

19386185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871868-G-A

19386185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871868-G-T

19386191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871874-G-A

19386191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871874-G-T

19386194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871877-A-G

19386201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871884-G-A

19386201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871884-G-T

19386255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871937-G-A

19386341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872022-C-T

http://identifiers.org/hco/13/GRCh38#19386408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56872087-C-A

19386453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872124-C-T

19386473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872144-G-C

19386473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872144-G-T

19386639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872287-A-G

19386680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872322-G-A

19386680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872322-G-C

19386770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872447-G-T

19386842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872520-T-C

19387017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873171-T-A

19387017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873171-T-C

19387017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873171-T-G

19387130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873288-A-G

19387148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873306-G-A

19387148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873306-G-T

19387610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875182-G-A

19387610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875182-G-T

http://identifiers.org/hco/13/GRCh38#19387635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875207-C-A

19387635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875207-C-T

http://identifiers.org/hco/13/GRCh38#19387642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875214-C-A

19387642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875214-C-G

19387642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875214-C-T

19387650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875221-T-C

19387715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875284-G-A

19387715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875284-G-T

19387745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56875307-T-A

19387745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56875307-T-G

http://identifiers.org/hco/13/GRCh38#19387823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875385-C-A

19387824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56875386-A-G

19387824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56875386-A-T

19387859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56875421-G-T

19387861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56875423-A-G

19387895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875450-T-C

http://identifiers.org/hco/13/GRCh38#19387900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875455-C-A

19387900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875455-C-T

19387959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56877071-G-A

19387959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56877071-G-T

19393924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56884484-G-A

19393973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56884529-G-A

19393973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56884529-G-T

19394072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56884621-T-C

http://identifiers.org/hco/13/GRCh38#19394090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56884639-A-C

19394090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884639-A-G

http://identifiers.org/hco/13/GRCh38#19394095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56884644-C-A

19394095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884644-C-T

19394104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884653-G-A

19394104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884653-G-T

19394105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884654-G-A

19394105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884654-G-T

19394109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56884658-G-T

19395455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56886397-A-G

19395455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56886397-A-T

19395591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886530-T-A

19395739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886618-T-G

19395756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886635-T-C

http://identifiers.org/hco/13/GRCh38#19395834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56886703-A-C

19395834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886703-A-G

19395944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887332-C-T

19397831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56889705-G-A

19397831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56889705-G-T

http://identifiers.org/hco/13/GRCh38#19402466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56892956-C-A

19402466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56892956-C-T

19402567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56893058-G-A

19402567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56893058-G-T

19402804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893380-A-G

19402898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893473-C-T

19407557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896479-G-A

19407709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896639-A-G

19407709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896639-A-T

19407776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56896701-T-C

19407776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56896701-T-G

19407804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56896729-G-A

19407804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37760
most severe consequence: non coding transcript exon variant
orthologous variants: 56896729-G-C