41626393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153780-G-A

41626393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153780-G-T

http://identifiers.org/hco/17/GRCh38#41626430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100153816-C-A

41626430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153816-C-T

41626434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153820-G-A

41626434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153820-G-T

41626471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153843-G-A

41626471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153843-G-T

41626522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100153882-G-A

41626548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 100153908-G-A

41626548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 100153908-G-T

http://identifiers.org/hco/17/GRCh38#41626612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100153974-C-A

http://identifiers.org/hco/17/GRCh38#41626684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154044-C-A

41626684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154044-C-T

http://identifiers.org/hco/17/GRCh38#41626685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154045-C-A

41626685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154045-C-T

41626688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154048-G-A

41626688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154048-G-T

41626756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154085-G-A

41626756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100154085-G-T

http://identifiers.org/hco/17/GRCh38#41626806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154136-C-A

41626806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154136-C-T

41626880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154208-C-T

http://identifiers.org/hco/17/GRCh38#41626988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154329-C-A

http://identifiers.org/hco/17/GRCh38#41627018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154359-A-C

41627019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154360-G-A

41627048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154387-A-T

41627051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154390-A-G

41627058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154397-G-T

http://identifiers.org/hco/17/GRCh38#41627077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154415-C-A

41627131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154469-G-A

41627131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154469-G-T

41627225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154560-A-G

http://identifiers.org/hco/17/GRCh38#41627226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154561-C-A

41627226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154561-C-G

41627240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154575-T-C

http://identifiers.org/hco/17/GRCh38#41627267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154620-A-C

http://identifiers.org/hco/17/GRCh38#41627272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154625-C-A

41627275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154645-T-C

http://identifiers.org/hco/17/GRCh38#41627316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154709-C-A

41627316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154709-C-T

http://identifiers.org/hco/17/GRCh38#41627435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154912-C-A

http://identifiers.org/hco/17/GRCh38#41627453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100154929-C-A

41627469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100154945-G-A

41627590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100155042-T-C

41627660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100155108-C-T

41627739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100155190-A-G

http://identifiers.org/hco/17/GRCh38#41627766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100155216-C-A

41627766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100155216-C-T

http://identifiers.org/hco/17/GRCh38#41628068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100155486-C-A

41628068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100155486-C-T

41628111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100155529-G-A

41628111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100155529-G-T

41628116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155534-A-G

41628146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155562-G-T

41628219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155618-G-A

41628219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155618-G-T

http://identifiers.org/hco/17/GRCh38#41628238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100155635-C-A

41628238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155635-C-T

41628287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155688-A-G

http://identifiers.org/hco/17/GRCh38#41628301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100155703-C-A

41628301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155703-C-T

41628316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155717-G-A

41628316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155717-G-T

http://identifiers.org/hco/17/GRCh38#41628327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100155728-C-A

41628327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155728-C-G

41628327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155728-C-T

41628334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155735-G-A

41628334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155735-G-T

41628339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100155740-G-T

41628434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100155845-T-C

41628467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100155878-T-A

41628467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100155878-T-C

41628467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100155878-T-G

41628489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100155899-A-G

41628597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100155997-A-G

41628844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156228-A-T

41628874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156256-G-A

http://identifiers.org/hco/17/GRCh38#41628921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156314-C-A

41628946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156336-G-A

41628946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156336-G-T

http://identifiers.org/hco/17/GRCh38#41628989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156369-C-A

41628989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156369-C-G

http://identifiers.org/hco/17/GRCh38#41629054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156405-C-A

41629054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156405-C-T

41629067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156417-G-A

41629067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156417-G-C

41629067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100156417-G-T

http://identifiers.org/hco/17/GRCh38#41629118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156468-C-A

41629118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156468-C-G

41629118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156468-C-T

http://identifiers.org/hco/17/GRCh38#41629181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156531-A-C

41629181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156531-A-G

41629184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156534-G-A

41629184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156534-G-T

41629196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100156546-A-G

http://identifiers.org/hco/17/GRCh38#41629197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156547-C-A

http://identifiers.org/hco/17/GRCh38#41629221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156571-C-A

http://identifiers.org/hco/17/GRCh38#41629315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100156655-A-C

41629316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156656-G-A

41629413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156730-G-T

41629433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156750-C-T

41629493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156801-C-T

41629495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156803-G-A

41629660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100156969-G-A

41629709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157018-G-A

41629921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157223-G-A

41630194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157473-C-G

41630194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157473-C-T

41630327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157676-A-G

41630332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157681-A-G

41630370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157721-T-C

41630370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157721-T-G

41630383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157725-G-C

41630383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100157725-G-T

41630467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157809-A-G

41630467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157809-A-T

http://identifiers.org/hco/17/GRCh38#41630476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100157818-C-A

41630476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157818-C-G

41630481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157823-G-A

41630481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157823-G-T

41630485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157827-G-A

41630485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157827-G-T

http://identifiers.org/hco/17/GRCh38#41630503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100157845-C-A

41630503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157845-C-T

http://identifiers.org/hco/17/GRCh38#41630509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100157851-C-A

41630509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157851-C-G

41630509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100157851-C-T

41630529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158011-G-A

41630529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158011-G-T

41630564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158046-A-G

41630576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158058-A-G

http://identifiers.org/hco/17/GRCh38#41630606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100158084-A-C

41630606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158084-A-T

http://identifiers.org/hco/17/GRCh38#41630607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100158085-A-C

41630607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100158085-A-G

http://identifiers.org/hco/17/GRCh38#41630688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100158168-C-A

41630688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100158168-C-G

http://identifiers.org/hco/17/GRCh38#41630702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100158188-C-A

41630702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100158188-C-T

http://identifiers.org/hco/17/GRCh38#41630745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100158219-C-A

41631414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100158630-C-T

41631434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100158649-C-T

41632019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159133-G-A

41632090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159173-G-A

41632136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159218-A-T

41632175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159257-C-T

http://identifiers.org/hco/17/GRCh38#41632252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100159337-C-A

41632252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159337-C-T

41632299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100159385-A-T

41633823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160395-A-G

41633823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160395-A-T

41633994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160568-G-A

41633994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160568-G-T

41634023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160602-G-A

41634023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160602-G-C

41634023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160602-G-T

http://identifiers.org/hco/17/GRCh38#41634035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100160614-C-A

41634053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160632-A-G

41634058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160637-T-C

41634065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160644-G-A

41634065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160644-G-T

http://identifiers.org/hco/17/GRCh38#41634073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100160652-C-A

41634073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160652-C-T

41634101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100160680-G-A

41634110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100160689-G-A

41634110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100160689-G-T

http://identifiers.org/hco/17/GRCh38#41634232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100160809-C-A

41634269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100160849-G-A

41634689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100160974-T-A

41634802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161088-A-G

41634838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161126-G-A

41634838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161126-G-C

http://identifiers.org/hco/17/GRCh38#41634924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100161195-C-A

41634924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161195-C-T

41635042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161294-T-C

http://identifiers.org/hco/17/GRCh38#41635214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100161697-C-A

41635214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161697-C-T

41635246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161728-G-A

41635246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161728-G-T

41635253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100161735-G-T

http://identifiers.org/hco/17/GRCh38#41635293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100161778-C-A

41635325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100161817-G-A

41635325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100161817-G-T

41635344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100161827-A-G

41635384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100161884-A-G

41635392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: non coding transcript exon variant
orthologous variants: 100161909-A-G

41635435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161958-G-A

41635435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161958-G-T

41635444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161961-C-G

41635444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161961-C-T

41635455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100161972-A-G

41635569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100162086-G-A

41635569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100162086-G-T

41636001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162506-C-T

41636068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162629-C-T

41636158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162712-G-A

41636360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162899-C-T

41636376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162917-C-G

41636376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162917-C-T

41636407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100162953-A-G

41636583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100163063-G-A

http://identifiers.org/hco/17/GRCh38#41636589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100163069-A-C

41636709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164612-G-T

41636789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164685-C-T

41636891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164753-G-A

41636891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164753-G-C

41636899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164768-G-A

41637070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100164899-G-T

41637169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165020-T-C

41638132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165420-T-C

41638339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165624-C-T

41638453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165755-T-C

41638648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165961-T-A

41638648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165961-T-C

41638651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165964-A-G

http://identifiers.org/hco/17/GRCh38#41638666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100165979-C-A

41638666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100165979-C-G