14911693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24769244-C-T

http://identifiers.org/hco/16/GRCh38#14911990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769629-A-C

14911990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24769629-A-G

14911990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24769629-A-T

14912078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769720-A-G

http://identifiers.org/hco/16/GRCh38#14912123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24769770-C-A

14912128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769775-C-T

14912143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769792-C-T

14912154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769810-G-A

14912154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24769810-G-T

http://identifiers.org/hco/16/GRCh38#14912448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24770054-A-C

14912448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770054-A-G

14912448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770054-A-T

14912572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770120-C-T

14912641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770193-C-T

14912759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770301-A-G

14912814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770325-G-A

14913226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24770789-G-A

14913243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770806-G-A

14913249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770812-C-G

14913249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770812-C-T

14913295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24770857-T-C

14913332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24770885-G-T

14913583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771075-G-A

14914060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771462-G-A

14914170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771562-C-T

14914215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771634-C-T

14914547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24771967-C-T

14917496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783084-C-G

14917510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783098-G-A

14917511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783099-G-A

14917511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783099-G-T

14917532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24783116-C-T

14917576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24783160-T-C

http://identifiers.org/hco/16/GRCh38#14918324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783789-A-C

http://identifiers.org/hco/16/GRCh38#14918359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24783831-A-C

14918398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-G-A

14918398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-G-C

14918398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783882-G-T

14918409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783935-G-A

14918493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784023-G-A

14918561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784091-C-T

http://identifiers.org/hco/16/GRCh38#14918726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784256-C-A

14918726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784256-C-T

14918735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784265-T-C

14918822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784352-T-A

14918822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784352-T-C

14918832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784362-A-G

14918832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784362-A-T

http://identifiers.org/hco/16/GRCh38#14918947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24784477-C-A

14918947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784477-C-T

14918975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-G-A

14918975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784505-G-T

14919031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784561-G-A

14919346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24784862-C-T

14919459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784974-G-A

14919478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784996-A-G

14919478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784996-A-T

14919487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785006-G-A

14919492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785013-T-G

14919604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785113-G-A

14919628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785138-A-G

14919908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786146-G-A

14919908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786146-G-T

14919925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786160-A-G

http://identifiers.org/hco/16/GRCh38#14919979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786214-A-C

14919979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786214-A-G

14919979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786214-A-T

14920075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-A

14920075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-C

14920075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24786310-G-T

14920203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786485-G-A

14920203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786485-G-T

14920208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786490-C-T

14920249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786547-T-A

14920249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786547-T-G

http://identifiers.org/hco/16/GRCh38#14920250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24786548-C-A

14920250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786548-C-G

14920256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786554-G-T

14920581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787007-G-A

14920705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787133-C-T

http://identifiers.org/hco/16/GRCh38#14921163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24787490-C-A

14921163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787490-C-G

http://identifiers.org/hco/16/GRCh38#14921174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24787501-A-C

14921221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787543-G-A

14921221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787543-G-T

14921300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24787623-G-A

14921346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24787654-C-G

14921346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24787654-C-T

14921376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24787684-G-A

http://identifiers.org/hco/16/GRCh38#14921515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24787823-C-A

14921515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24787823-C-T

http://identifiers.org/hco/16/GRCh38#14921660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24787969-C-A

14921660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24787969-C-G

14921660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24787969-C-T

14921715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788038-G-A

14921798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788121-T-C

14921949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788272-C-T

14921972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788296-G-A

14921972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788296-G-C

14922125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788447-C-T

14922364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788686-G-C

14922364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788686-G-T

http://identifiers.org/hco/16/GRCh38#14922409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24788731-C-A

14922409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788731-C-G

14922534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-G-A

14922534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24788856-G-T

14922962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24789369-C-T

http://identifiers.org/hco/16/GRCh38#14923008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24789429-C-A

14923008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24789429-C-T

14923031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24789452-C-T

http://identifiers.org/hco/16/GRCh38#14923047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24789467-C-A

14923047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24789467-C-T

14923383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789782-C-T

14923485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24789903-G-T

14923548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790037-T-C

http://identifiers.org/hco/16/GRCh38#14923649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790148-C-A

14923649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790148-C-G

14923649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24790148-C-T

14923723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24790222-C-T

14924009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24790527-C-T

14924198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790707-C-T

14924290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790790-G-A

14924389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790883-G-A

14924408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790896-G-T

14924409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790897-G-T

http://identifiers.org/hco/16/GRCh38#14924419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790907-A-C

http://identifiers.org/hco/16/GRCh38#14924420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24790908-C-A

14924420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790908-C-T

14924426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-A

14924426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-C

14924426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790914-G-T

14924473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-G-A

14924473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790921-G-C

14924485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790933-G-A

14924485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790933-G-C

14924485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790933-G-T

14924495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790940-G-A

14924495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24790940-G-T

14924559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24791004-C-G

14924559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24791004-C-T

http://identifiers.org/hco/16/GRCh38#14924592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24791037-C-A

14924592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24791037-C-G

14924592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24791037-C-T

14924644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791089-G-T

http://identifiers.org/hco/16/GRCh38#14924728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24791159-C-A

14924728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24791159-C-T

14925861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24796621-C-T

14925981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796692-C-T

http://identifiers.org/hco/16/GRCh38#14926060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796780-A-C

14926060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24796780-A-G

http://identifiers.org/hco/16/GRCh38#14926184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24796904-C-A

14926184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24796904-C-T

http://identifiers.org/hco/16/GRCh38#14926419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797112-C-A

14926483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24797176-C-T

14926580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-A

14926580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24797273-G-T

http://identifiers.org/hco/16/GRCh38#14926643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24797338-C-A

14926643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24797338-C-G

14926643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24797338-C-T

14926653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24797349-G-A

14926723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24797419-G-A

http://identifiers.org/hco/16/GRCh38#14928269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798579-C-A

14928269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798579-C-G

14928269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798579-C-T

http://identifiers.org/hco/16/GRCh38#14928280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798589-C-A

14928280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798589-C-T

14928303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798612-T-A

14928303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798612-T-C

14928303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798612-T-G

14928305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798614-A-G

14928313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798628-T-C

14928313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798628-T-G

14929169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24798859-C-G

http://identifiers.org/hco/16/GRCh38#14929264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798942-C-A

14929264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24798942-C-T

http://identifiers.org/hco/16/GRCh38#14929312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24798990-C-A

14929312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24798990-C-T

14929318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24798996-A-T

14929370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-C-G

14929370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24799048-C-T

14929759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24799438-G-A

14929786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24799465-G-C

14930008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24799683-G-T

14930070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799768-G-T

14930106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799788-G-T

http://identifiers.org/hco/16/GRCh38#14930379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24800070-C-A

14930379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800070-C-T

14930491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800154-T-C

14930584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800246-G-A

14930584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800246-G-C

14930584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800246-G-T

http://identifiers.org/hco/16/GRCh38#14930686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24800348-C-A

14930686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800348-C-T

14930707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800369-C-G

14930707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800369-C-T

14930834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800487-A-G

14930834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800487-A-T

14930871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800528-T-G

14931008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24800665-C-T

14931085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-G-A

14931085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-G-C

14931085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800742-G-T

14931101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800766-G-A

14931101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800766-G-T

14931528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801158-C-T

14931540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801170-C-T

14931700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801320-C-T

14931735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801354-G-A

14931759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801359-C-G

14931859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801444-C-T

14931915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801505-C-T

14932572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24804652-T-G

http://identifiers.org/hco/16/GRCh38#14932575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24804655-C-A

14932575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804655-C-T

14932677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804757-C-G

14932677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804757-C-T

14932692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-G-A

14932692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-G-C

14932692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804772-G-T

14932748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24804828-A-G

14932752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804843-A-G

14932853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24804922-G-A

14932974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805043-A-G

http://identifiers.org/hco/16/GRCh38#14933026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805091-C-A

14933026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805091-C-G

14933026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805091-C-T

14933032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805097-G-A

14933075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24805147-C-T

http://identifiers.org/hco/16/GRCh38#14933076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24805148-C-A

14933373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24805442-G-T

14933430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24805499-C-T

14933607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805654-G-A

14933607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805654-G-C

14933698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805743-A-G

14933731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805802-A-G

14933887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24805906-G-A

14935337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24806363-C-T

14935359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: non coding transcript exon variant
orthologous variants: 24806385-A-G

14935465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-A

14935465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806496-G-T

http://identifiers.org/hco/16/GRCh38#14935475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806506-C-A

14935475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806506-C-G

14935475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806506-C-T

http://identifiers.org/hco/16/GRCh38#14935610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806612-C-A

14935610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24806612-C-T

http://identifiers.org/hco/16/GRCh38#14935637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806639-C-A

14935637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806639-C-T

http://identifiers.org/hco/16/GRCh38#14935640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24806642-C-A

14935640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24806642-C-T