74262814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102140520-A-G

74262848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102140573-A-G

http://identifiers.org/hco/3/GRCh38#74263082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102140816-C-A

74263185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102140906-C-T

74263252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102140974-T-G

74263365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141088-T-C

74263520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141247-T-A

74263520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141247-T-C

74263674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141483-T-C

74263884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141687-G-T

74263974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141766-A-G

http://identifiers.org/hco/3/GRCh38#74264037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102141813-C-A

74264037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141813-C-G

74264037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141813-C-T

74264101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141883-G-T

74264113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141895-G-A

74264113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102141895-G-C

http://identifiers.org/hco/3/GRCh38#74264165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102142042-C-A

74264165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142042-C-G

74264165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142042-C-T

74264345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142218-A-G

http://identifiers.org/hco/3/GRCh38#74264363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102142241-C-A

74264363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142241-C-T

74264382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142260-T-A

74264382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 3 prime UTR variant
orthologous variants: 102142260-T-C

74264440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102142318-C-T

http://identifiers.org/hco/3/GRCh38#74264567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102142435-C-A

http://identifiers.org/hco/3/GRCh38#74264589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102142454-C-A

74264589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102142454-C-T

74264996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144019-A-G

http://identifiers.org/hco/3/GRCh38#74265046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102144068-C-A

74265050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144073-T-G

74265190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144198-A-T

74265398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144425-G-A

74265536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144761-T-C

74265665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102144905-C-T

74266107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145350-A-T

74266150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145520-G-A

74266182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145590-T-A

74266271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145672-T-C

74266277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145678-C-T

74266309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145694-C-T

74266348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145733-G-A

74266348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145733-G-T

74266406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145779-G-A

74266406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145779-G-T

74266436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145809-T-A

74266436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102145809-T-C

74266614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102145987-T-C

74266614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102145987-T-G

74266701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102146070-T-C

http://identifiers.org/hco/3/GRCh38#74266792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102146147-C-A

http://identifiers.org/hco/3/GRCh38#74266884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102146238-C-A

74266905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102147187-C-T

http://identifiers.org/hco/3/GRCh38#74267194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102147470-C-A

74267198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102147475-T-C

74267198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102147475-T-G

http://identifiers.org/hco/3/GRCh38#74267210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102147487-C-A

74267210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102147487-C-T

74267226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102147503-A-G

74267417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102147688-G-T

74267478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102147744-A-T

http://identifiers.org/hco/3/GRCh38#74267479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102147745-C-A

74267479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102147745-C-G

74267479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102147745-C-T

74267752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148024-C-T

74267810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148081-C-T

74267925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148198-T-G

74267974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148246-T-G

74267986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148258-C-T

74267992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148264-G-A

http://identifiers.org/hco/3/GRCh38#74268005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102148277-A-C

74268023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148299-G-A

74268023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148299-G-C

74268023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148299-G-T

74268200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148475-G-A

74268257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148576-T-G

74268315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148629-T-C

74268381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148708-G-T

74268566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148886-G-T

74268612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148937-G-A

74268690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102148998-C-G

74268703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149011-T-G

74268786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149093-C-T

74268884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149198-G-T

74268910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149224-T-C

http://identifiers.org/hco/3/GRCh38#74268947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102149248-A-C

74270692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149420-C-G

74270744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149471-T-A

74270814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149522-C-T

74270820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149528-T-C

74270822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149530-T-C

74270880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149602-T-C

74270881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149603-G-C

74270881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149603-G-T

http://identifiers.org/hco/3/GRCh38#74271032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102149756-A-C

http://identifiers.org/hco/3/GRCh38#74271048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102149772-C-A

74271136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149864-C-T

74271186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149905-A-G

74271188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149907-G-A

74271205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102149924-T-C

74271513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150601-G-A

74271710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150803-C-T

74271768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150861-G-C

74271804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150890-G-A

74271820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150902-A-G

74271834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150912-T-C

74271927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102150987-T-A

74281762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160467-T-C

74281784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160486-G-A

74281792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160496-C-G

74281902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160598-C-T

74281921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160616-G-A

74282023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160722-T-G

74282131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160828-C-T

74282163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160859-T-C

74282283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102160980-A-G

74282521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161231-C-T

http://identifiers.org/hco/3/GRCh38#74282649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102161356-A-C

74283108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161789-C-T

74283164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161842-G-A

74283165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161843-G-A

74283251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161917-G-A

74283331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102161996-A-G

74283356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102162021-G-A

74283648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102162523-G-A

http://identifiers.org/hco/3/GRCh38#74283686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102162556-A-C

74283782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102162649-C-T

74284007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102162868-T-C

http://identifiers.org/hco/3/GRCh38#74284666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102163433-A-C

74284833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163600-A-T

74284943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163690-A-T

http://identifiers.org/hco/3/GRCh38#74284952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102163699-A-C

74285046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163772-G-C

74285067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163787-C-T

74285220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163909-T-A

74285220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163909-T-C

74285220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163909-T-G

74285282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102163970-C-T

74285306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 102164002-C-T

74285321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102164017-T-C

74285321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102164017-T-G

74285336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102164032-G-A

74285351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102164047-G-A

74285351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102164047-G-T

74285487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: 102164183-C-T

74285569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102164270-G-A

74285610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102164313-G-T

74285667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102164368-G-C

74285688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102164391-A-G

74285786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102164483-G-A

74286008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102167530-A-T

74286084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102167606-T-C

74286538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168018-T-C

74286631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168107-G-A

74286748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168222-C-T

74286823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168282-C-T

74286840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168298-C-T

74286845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168303-G-A

74287085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102168938-C-T

74287192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169032-T-G

74287234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169082-T-A

74287247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169095-A-G

http://identifiers.org/hco/3/GRCh38#74287438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102169292-C-A

74287509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169363-T-C

74287509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169363-T-G

74287566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169423-A-G

74287606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169462-G-A

74287668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169520-T-C

74287783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169604-C-T

74287788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169609-A-T

74288132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169926-G-T

74288139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102169933-T-G

74288582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102170053-C-T

74289009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102171882-A-G

74289070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102171943-G-C

http://identifiers.org/hco/3/GRCh38#74289086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102171958-A-C

74289190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172059-T-A

74289304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172178-G-A

74289462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172333-T-C

74289709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172616-G-A

74289715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172622-G-A

74289715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172622-G-T

74289821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172672-T-A

74289937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102172776-G-A

74291689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173396-A-T

74291769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173475-G-A

74291838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173543-G-A

74291987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173665-T-C

74292044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173703-A-G

74292234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102173898-G-A

74293091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102174841-T-C

74293362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175091-C-T

74294522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175604-G-C

74294579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175657-A-G

74294622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175699-G-T

74294707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175779-G-T

74294854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102175941-A-G

http://identifiers.org/hco/3/GRCh38#74295016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102176087-C-A

74295016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102176087-C-T

74295116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102176192-A-G

74295263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102176348-G-T

74295354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102176904-T-C

74295368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102176914-T-C

74295637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102177173-G-A

74295637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102177173-G-C

74296191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102177683-C-T

http://identifiers.org/hco/3/GRCh38#74296208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102177702-C-A

74296231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102177722-G-A

74296328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102177818-A-G

74296713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178209-T-A

74296793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178288-T-C

74296896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178393-T-A

74296897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178394-G-T

74296903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178400-G-T

74296922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178420-C-T

74296931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178429-G-A

74297057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178549-G-A

74297065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178557-G-C

74297081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178575-G-A

74297170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178662-G-C

74297184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178676-T-C

74297274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102178764-G-A

74297970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102180806-G-A

74297994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102180830-T-C

74298186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102181022-G-C

74298238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181077-G-A

74298238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181077-G-T

http://identifiers.org/hco/3/GRCh38#74298247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102181086-A-C

74298252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181091-A-G

74298341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181177-T-C

74298434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181269-C-G

74298531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181363-T-C

74298540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181373-T-C

http://identifiers.org/hco/3/GRCh38#74298541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102181374-A-C

74298555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181389-G-A

http://identifiers.org/hco/3/GRCh38#74299327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102181581-C-A

74299369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181627-A-G

74299591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102181846-G-C

74299725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183325-T-G

74299733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183333-G-A

74299733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183333-G-C

74299733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183333-G-T

http://identifiers.org/hco/3/GRCh38#74299773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102183390-C-A

74299773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183390-C-T

http://identifiers.org/hco/3/GRCh38#74299792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102183409-C-A

74299792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183409-C-T

http://identifiers.org/hco/3/GRCh38#74299799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102183416-A-C

74299799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183416-A-G

74299810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183429-C-T

http://identifiers.org/hco/3/GRCh38#74299929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102183549-A-C

74299929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: 102183549-A-G

74299947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183567-G-T

74299953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183573-G-A

74299953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183573-G-T

74299983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183603-G-A

74299983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183603-G-C

74299983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183603-G-T

74300041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183658-T-C

74300104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183755-A-G

74300104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183755-A-T

74300137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102183792-C-T

74300607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184235-C-T

74300665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184295-T-A

74300828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184461-T-C

74301121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184746-G-A

74301250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184875-A-T

74301266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184891-C-T

74301325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184946-G-A

74301325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102184946-G-T

74301603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185231-T-A

74301814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185442-G-A

http://identifiers.org/hco/3/GRCh38#74301885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102185498-C-A

74301885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185498-C-T

74301886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185499-A-G

74302049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185641-C-T

74302190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185772-A-G

http://identifiers.org/hco/3/GRCh38#74302194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102185776-C-A

74302298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185883-G-A

74302301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185886-T-A

74302301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185886-T-C

74302411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185941-A-T

74302421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102185951-C-T

74302490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186020-C-G

74302633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186144-G-T

74302655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186171-G-A

74302655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186171-G-C

74302739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102186249-C-T

74303010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186489-T-C

74303100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186573-T-C

74303118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186590-C-G

74303118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186590-C-T

74303260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186731-A-G

74303260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186731-A-T

74303261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186732-T-C

74303369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102186840-T-C

74304033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187224-A-T

74304091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187282-G-A

74304164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187355-T-A

74304343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187531-G-A

74304739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187931-G-A

74304739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102187931-G-C

74304834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102188269-T-A

74304902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102188336-A-G

74305031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102188430-A-T

74306441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102194857-A-G

74306480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102194894-T-A

74306480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102194894-T-G

74306523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102194937-A-G

74306540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102194941-T-C

http://identifiers.org/hco/3/GRCh38#74306611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102195012-A-C

74306633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102195035-T-C

74306828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102195224-C-T

74306918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102195307-G-C

74307061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102195450-A-G

74307329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198178-T-C

74307332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198181-A-T

74307371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198211-T-A

74307433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198268-T-G

74307465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198299-C-G

74307515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198334-A-G

74308047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198861-C-G

74308047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102198861-C-T

74308223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102199037-C-T

74308353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102199165-T-C

74308894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102199691-A-G

http://identifiers.org/hco/3/GRCh38#74309038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102199833-C-A

74309038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102199833-C-T

74309565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200234-A-G

74309636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200303-T-C

74309667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200332-T-C

74309753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200414-T-C

74309813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200559-T-C

74309830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200584-G-A

74309869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200623-C-T

74310069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102200818-A-G

74310454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201155-T-C

74310478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201179-T-C

74310507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201208-G-A

74310539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201240-G-A

74310609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201300-T-C

74310803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201444-G-A

http://identifiers.org/hco/3/GRCh38#74310821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102201462-C-A

74310871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201511-C-T

74310958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201614-C-T

74311182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201860-T-C

74311252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201930-A-T

74311260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102201938-T-G

74311508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102202161-C-T

74311545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102202192-G-A

74328491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213611-T-G

74328583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213713-C-T

74328602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213734-A-T

74328631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213761-A-T

74328687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213815-T-C

74328739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213867-T-A

74328846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102213976-A-G

74328968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214082-G-A

74329044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214188-T-C

http://identifiers.org/hco/3/GRCh38#74329158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102214300-C-A

74329163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214305-A-T

74329198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214340-T-C

74329226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214368-G-C

74329532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214765-G-T

74329577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102214812-G-A

74331526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215498-T-G

74331662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215627-C-T

74331709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215673-G-C

74331829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215796-T-G

74331840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215807-G-C

74331916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102215871-C-T

http://identifiers.org/hco/3/GRCh38#74332046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102216005-A-C

74332046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216005-A-T

74332186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216078-G-A

http://identifiers.org/hco/3/GRCh38#74332670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102216553-A-C

74332670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216553-A-G

74332934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216822-T-A

74332934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216822-T-C

74332994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102216869-G-A

74333206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217076-G-A

74333206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217076-G-T

74333210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217080-T-C

74333455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217321-G-A

74333573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217427-G-A

http://identifiers.org/hco/3/GRCh38#74333598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102217452-C-A

74333720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217579-A-G

74333720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217579-A-T

74334027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217863-T-C

74334038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102217874-G-C

74334152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102218442-C-T

http://identifiers.org/hco/3/GRCh38#74334618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102218866-A-C

74334673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102218897-C-T

74334697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102218913-T-C

74334831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: 102219047-T-A

74334831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102219047-T-C

74335001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219230-T-C

http://identifiers.org/hco/3/GRCh38#74335057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102219279-C-A

74335057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219279-C-T

74335143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219377-T-C

74335293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219512-A-G

74335387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219585-C-T

74335422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219620-C-T

http://identifiers.org/hco/3/GRCh38#74335434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102219632-C-A

74335486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219677-T-A

http://identifiers.org/hco/3/GRCh38#74335626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102219812-C-A

74335650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219838-C-G

74335650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219838-C-T

74335667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102219854-G-T

http://identifiers.org/hco/3/GRCh38#74335743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102221068-C-A

74336415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102221823-T-C

74336489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102221973-A-G

http://identifiers.org/hco/3/GRCh38#74336722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102222193-C-A

74336739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102222210-T-C

74336740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102222211-G-A

74336740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102222211-G-T

http://identifiers.org/hco/3/GRCh38#74336798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102222267-A-C

74338058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102223023-T-A

74338058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102223023-T-G

74338169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102223141-G-A

74338272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102223244-C-T

74340317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102224826-G-C

74340344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102224853-T-A

http://identifiers.org/hco/3/GRCh38#74340346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102224855-A-C

74340507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102225026-C-T

74340546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102225045-T-C

74340800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102225273-G-A

74341198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102225740-G-A

74341280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102225823-C-T

74341632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226183-G-A

74341632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226183-G-C

74341869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226437-C-T

74341988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226553-G-A

74342079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226646-A-T

http://identifiers.org/hco/3/GRCh38#74342099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102226666-C-A

74342178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226745-A-T

http://identifiers.org/hco/3/GRCh38#74342256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102226784-C-A

74342276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226801-C-G

74342276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226801-C-T

74342350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102226874-A-G

74342789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227292-A-G

74343294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227727-C-T

74343348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227784-C-G

74343379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227815-G-A

74343384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227820-C-G

74343554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102227965-A-G

74343603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228012-T-C

74344371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, undefined
orthologous variants: 102228484-T-C

http://identifiers.org/hco/3/GRCh38#74344382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#102228495-C-A

74344382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, undefined
orthologous variants: 102228495-C-T

74344921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228617-G-T

74344922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228618-A-G

74344970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228667-G-A

74344975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228672-C-G

74344977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228674-A-G

74344978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228675-T-C

74344996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228690-G-A

74345151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228849-A-T

74345196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102228892-G-A

74345455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102229077-G-C

74345737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102229339-C-T

74346242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102231646-A-G

74346418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102231986-T-C

74346426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102231994-G-A

74346426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102231994-G-T

74346501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232083-C-G

74346501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232083-C-T

74346504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232084-A-G

http://identifiers.org/hco/3/GRCh38#74346898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102232463-A-C

74346966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232527-C-G

74346966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232527-C-T

74347110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232677-C-T

http://identifiers.org/hco/3/GRCh38#74347214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102232782-A-C

74347273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102232845-G-A

http://identifiers.org/hco/3/GRCh38#74347774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102233340-C-A

74347774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102233340-C-T

74349579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234613-C-T

74349586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234620-T-C

74349645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234669-T-C

74349689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234710-T-C

74349730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234738-A-T

74349767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234773-G-A

74349767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234773-G-C

74349964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102234959-C-T

74350018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235011-C-G

74350018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235011-C-T

74350058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235051-A-T

74350106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235098-C-T

http://identifiers.org/hco/3/GRCh38#74350252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102235243-C-A

74350263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235249-G-C

74350265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102235251-T-C

74353926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237198-C-T

http://identifiers.org/hco/3/GRCh38#74353964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102237245-C-A

74354019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237297-A-G

74354119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237394-T-A

74354134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237409-G-T

74354183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237467-G-A

74354401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237678-A-G

74354401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102237678-A-T

74354934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238144-A-T

http://identifiers.org/hco/3/GRCh38#74357799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102238474-A-C

74357799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238474-A-G

74358016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238702-T-C

74358025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238711-G-C

74358159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238840-A-G

74358209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102238890-G-A

74359209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102239315-C-G

74359243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102239354-T-A

74359308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102239418-T-C

74359315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102239425-A-G

74360055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240018-T-A

74360109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240068-G-A

74360116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240075-C-T

74360268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240218-T-C

74360293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240243-A-G

74360319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240270-G-C

74360356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240306-T-C

74360394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240344-C-T

74360695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240552-G-A

74360707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240564-C-T

74360790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102240629-G-A

74361186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102241598-C-T

74361197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102241609-G-A

74361389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102241807-G-A

http://identifiers.org/hco/3/GRCh38#74361498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102241911-A-C

74361573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102241985-G-A

74361632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242044-G-A

74361638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242050-G-T

http://identifiers.org/hco/3/GRCh38#74361785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102242180-C-A

74361785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242180-C-T

74361806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242200-T-A

74362052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242442-G-A

74362072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242462-G-A

74362124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242709-A-G

http://identifiers.org/hco/3/GRCh38#74362155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102242740-C-A

74362155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242740-C-T

74362190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242783-G-A

74362190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102242783-G-T

74363874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243554-T-C

74364007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243691-G-A

74364007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243691-G-C

74364089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243773-T-C

74364252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243930-T-C

74364252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243930-T-G

http://identifiers.org/hco/3/GRCh38#74364272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102243949-C-A

74364272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102243949-C-G

http://identifiers.org/hco/3/GRCh38#74364330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102244197-C-A

74364330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244197-C-G

74364330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244197-C-T

74364420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244286-G-C

74364420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244286-G-T

74364425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244291-A-G

http://identifiers.org/hco/3/GRCh38#74364430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102244296-A-C

74364442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244308-G-A

http://identifiers.org/hco/3/GRCh38#74364699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102244553-C-A

74364711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244565-G-C

74364711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244565-G-T

74364729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244583-T-C

74364729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244583-T-G

http://identifiers.org/hco/3/GRCh38#74364732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102244586-A-C

74364735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244589-T-C

http://identifiers.org/hco/3/GRCh38#74364740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102244594-C-A

74364764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244618-T-C

74364917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244724-A-G

74364917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102244724-A-T

74365174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102245002-C-T

74365776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102246270-A-G

74365838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102246319-G-T

74366470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102246945-A-G

74366481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102246956-T-C

74366710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247196-C-G

74366809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247220-A-G

74366809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247220-A-T

74366815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247226-T-C

74366900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247308-G-A

74366900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247308-G-T

http://identifiers.org/hco/3/GRCh38#74366927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102247334-C-A

74366927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247334-C-T

http://identifiers.org/hco/3/GRCh38#74366950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102247357-C-A

74366950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247357-C-G

74366950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247357-C-T

http://identifiers.org/hco/3/GRCh38#74366957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102247364-C-A

74366957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247364-C-T

74366975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247373-T-A

74366977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247375-C-T

74366999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247402-C-T

74367029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247431-C-T

http://identifiers.org/hco/3/GRCh38#74367129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102247531-A-C

74367129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247531-A-G

74367166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247568-C-T

74367187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247593-T-C

74367271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247676-C-G

74367271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247676-C-T

74367323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247703-A-T

74367327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247707-T-C

74367374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247762-T-A

74367391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247779-T-G

74367463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247863-C-G

74367463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247863-C-T

74367603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102247988-T-G

74368059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102249099-T-C

74368063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102249103-C-T

74368265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102249720-G-T

http://identifiers.org/hco/3/GRCh38#74368409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102249865-C-A

74368409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102249865-C-T

http://identifiers.org/hco/3/GRCh38#74368656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102250096-A-C

74368671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250111-T-A

74368671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250111-T-C

74368995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250410-G-A

74369028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250437-A-T

74369081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250503-G-T

74369092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250514-G-A

74369092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250514-G-T

74369142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250554-G-T

74369150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250562-A-G

http://identifiers.org/hco/3/GRCh38#74369166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102250578-A-C

74369166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250578-A-G

http://identifiers.org/hco/3/GRCh38#74369171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102250583-C-A

74369171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250583-C-T

74369228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: stop gained
orthologous variants: 102250640-G-A

74369228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102250640-G-T

74369244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102250656-G-A

http://identifiers.org/hco/3/GRCh38#74369289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102250701-A-C

74369331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102250743-T-A

http://identifiers.org/hco/3/GRCh38#74369401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102250813-C-A

74369401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250813-C-T

74369452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250865-A-T

74369484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102250892-C-T

74369796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254105-G-C

74369796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254105-G-T

74369801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254110-T-C

74369867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254158-G-A

74369867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254158-G-T

74370001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254292-C-T

http://identifiers.org/hco/3/GRCh38#74370141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102254422-C-A

74370141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254422-C-T

http://identifiers.org/hco/3/GRCh38#74370525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102254653-C-A

74370617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254742-A-G

74370626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254750-G-A

74370702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102254826-C-T

74371060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255144-A-T

74371164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255221-G-A

74371164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255221-G-T

74371203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102255246-A-G

74371251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: 102255294-C-G

74371269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102255312-T-G

http://identifiers.org/hco/3/GRCh38#74371347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102255390-A-C

74371347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102255390-A-G

74371531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255536-G-A

74371531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255536-G-C

http://identifiers.org/hco/3/GRCh38#74371585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102255589-A-C

74371605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255609-T-C

74371673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255683-G-A

74371733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255734-T-G

74371899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102255867-G-A

74372269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102257857-C-T

74372275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102257863-G-C

74372309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102257891-A-G

74372333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102257916-G-T

http://identifiers.org/hco/3/GRCh38#74372370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102257951-C-A

74372425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258002-T-A

74372425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258002-T-C

74372452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258029-G-T

74372460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258037-C-G

74372467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258043-G-A

http://identifiers.org/hco/3/GRCh38#74372468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102258044-A-C

74372481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258057-G-T

74372608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258168-T-C

74372656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258233-T-C

74372670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258247-T-C

74372686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258259-C-T

74372782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258347-G-A

74372908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258470-A-G

74372973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258520-C-T

74373049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258573-G-A

74373233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258736-A-G

74373279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102258782-G-A

74373477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259031-G-A

74373565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259123-C-T

74373780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259335-A-G

74373796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259349-C-G

74373931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259442-T-A

74373932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259443-T-A

74373933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259444-C-G

74373976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259491-A-T

74374009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259506-A-T

http://identifiers.org/hco/3/GRCh38#74374011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102259508-C-A

74374011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259508-C-T

74374035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259532-G-A

74374091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259587-T-A

74374118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259614-G-A

74374122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259617-C-T

http://identifiers.org/hco/3/GRCh38#74374282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102259749-A-C

74374282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259749-A-G

74374282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102259749-A-T

74374533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260019-T-A

http://identifiers.org/hco/3/GRCh38#74374720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102260164-C-A

74374720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260164-C-T

74374796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260239-T-C

74374796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260239-T-G

74374851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260292-A-T

74375016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260466-T-C

74375072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260522-T-C

74375125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260553-C-T

http://identifiers.org/hco/3/GRCh38#74375329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102260719-C-A

74375351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102260743-G-A

74375406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262286-G-A

74375462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262337-T-G

http://identifiers.org/hco/3/GRCh38#74375476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102262350-A-C

74375581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262458-G-A

74375617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262494-C-T

74375659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262536-T-G

74375753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262604-T-G

74375832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262691-C-T

74375910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102262761-G-A

74376743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102263491-G-A

74376810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102263561-T-C

74376871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102263576-G-A

74376871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102263576-G-T

74376957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102263632-T-A

74377435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264077-A-G

74377693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264322-A-G

http://identifiers.org/hco/3/GRCh38#74377704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102264333-A-C

74377779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264410-T-C

74377928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264558-T-C

74378170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264800-C-T

http://identifiers.org/hco/3/GRCh38#74378174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102264804-C-A

74378344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264933-G-A

74378344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264933-G-T

74378366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264960-G-T

74378369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264963-T-C

74378375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264969-G-A

74378402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102264986-T-C

74378439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265023-A-G

74378703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265326-G-A

74378785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265377-T-C

74378976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265552-G-A

74378992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265568-T-G

74379015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265603-C-T

74379017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265605-C-T

74379079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102265652-T-C

http://identifiers.org/hco/3/GRCh38#74379692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102266086-C-A

74379692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102266086-C-T

74379902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102266274-A-G

74380030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102266407-T-C

74380030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102266407-T-G

74380198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102266857-T-C

http://identifiers.org/hco/3/GRCh38#74380462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102267119-C-A

74380807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102267462-A-G

74380938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102267589-A-G

74381053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102267896-G-T

74381341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102268489-G-C

74381518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102268673-G-C

74381597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102268747-T-C

74381669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102268814-G-C

74383905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102271434-A-G

74384171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102271729-C-T

74384220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102271790-C-T

74384376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102271940-A-T

http://identifiers.org/hco/3/GRCh38#74384540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102272104-A-C

74384709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272306-C-T

74384745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272339-T-C

74384797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272391-G-A

http://identifiers.org/hco/3/GRCh38#74384810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102272404-C-A

74384892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272486-T-A

74384923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272517-A-G

74384954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272547-T-A

74384985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272578-T-C

74384991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272584-C-T

74385107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102272693-T-C

74385469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102273044-T-C

http://identifiers.org/hco/3/GRCh38#74385499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102273077-C-A

74385499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102273077-C-T

74385523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102273099-C-T

74385578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102273151-T-C

74385682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102273225-T-C

74386247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102274519-T-A

74386247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102274519-T-C

74386258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102274527-C-G

74386758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102275479-T-C

74386764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102275485-C-T

74386854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102275568-C-T

74386863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102275577-C-T

http://identifiers.org/hco/3/GRCh38#74387162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102275851-C-A

74387192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102275870-G-T

74387713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102276333-T-C

74387979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102276609-G-A

74388318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102278496-T-G

74388364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102278539-A-T

http://identifiers.org/hco/3/GRCh38#74388640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102278797-C-A

74388648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102278805-G-C

74388750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102278916-C-T

http://identifiers.org/hco/3/GRCh38#74388890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102279035-A-C

74388890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279035-A-T

74388892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279037-G-C

74388892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279037-G-T

http://identifiers.org/hco/3/GRCh38#74389037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102279178-C-A

74389045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279186-G-A

http://identifiers.org/hco/3/GRCh38#74389156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102279301-C-A

74389325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279464-T-C

74389703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279792-G-A

74389703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279792-G-C

74389703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102279792-G-T

74390013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102280051-C-T

74390124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102280554-G-C

http://identifiers.org/hco/3/GRCh38#74390408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102280821-C-A

74390408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102280821-C-T

74390908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102281364-T-C

74391303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102281708-T-C

74391933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102282311-C-G

http://identifiers.org/hco/3/GRCh38#74392034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102282392-C-A

74392034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102282392-C-T

74392049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102282407-G-A

74393358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102285644-T-G

74393384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102285667-T-C

74393683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102285955-C-T

74393887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102286156-T-C

74394086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102286355-T-C

74394218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102286486-G-A

74394588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287039-A-G

74394719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287182-A-G

74394930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287401-T-C

74395072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287535-A-G

74395376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287849-C-T

74395417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102287891-T-C

http://identifiers.org/hco/3/GRCh38#74400300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102290840-C-A

74400300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102290840-C-T

74401346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292557-T-C

74401346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292557-T-G

74401531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292659-C-G

74401533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292661-G-C

74401724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292861-G-C

74401834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102292976-A-G

74401917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293062-C-T

74401944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293087-A-G

74402009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293146-G-T

74402046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293175-G-C

http://identifiers.org/hco/3/GRCh38#74402201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102293340-A-C

74402236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293373-C-G

74402337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102293480-C-T

http://identifiers.org/hco/3/GRCh38#74402352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102293494-C-A

74407100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102296528-T-A

74407167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102296604-T-A

74407167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102296604-T-C

74408139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102297108-C-T

74408518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102297408-C-T

74409033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298042-G-T

http://identifiers.org/hco/3/GRCh38#74409034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102298043-C-A

74409034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298043-C-T

74409053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298062-C-T

74409287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298260-C-T

74409443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298423-T-C

74409462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298441-A-G

74409828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102298811-T-C

74409912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102299000-T-C

74409990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102299080-T-C

74410397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102299467-T-C

74411057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102300131-A-T

74411280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102300986-C-T

74411405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102301099-C-T

http://identifiers.org/hco/3/GRCh38#74411535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102301206-C-A

74411535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102301206-C-T

74411840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102301517-T-C

74412184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102302258-T-A

74412404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102302476-T-C

74412591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102302658-A-T

74413853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102303700-G-C

74414009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102303850-A-G

74414316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102304090-A-G

74414824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305311-C-T

74414825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305312-A-G

74414873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305355-T-C

74414940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305383-A-G

74414940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305383-A-T

74414976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305437-C-G

74415082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305552-C-T

74415084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305554-A-T

http://identifiers.org/hco/3/GRCh38#74415085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102305555-C-A

74415111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102305580-C-T

74415301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102306716-G-C

http://identifiers.org/hco/3/GRCh38#74415380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102306793-C-A

74415380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102306793-C-G

http://identifiers.org/hco/3/GRCh38#74415422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102306826-C-A

74415506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102306898-T-C

74415850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102307177-A-T

74415851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102307178-C-T

74415892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102307219-A-T

74415981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102307326-G-C

74417562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308298-C-G

74417593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308332-G-A

74417593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308332-G-C

74417629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308371-C-T

74417764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308483-T-C

74417974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308688-T-C

74417982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308696-T-C

74418003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308717-T-C

74418012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102308726-T-C

74419351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102309133-G-A

74419455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102309234-T-C

http://identifiers.org/hco/3/GRCh38#74419608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102309383-C-A

74419798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102309566-C-T

74419824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102309593-T-G

74420172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102309931-G-A

74420265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102310024-A-G

http://identifiers.org/hco/3/GRCh38#74420671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102312775-A-C

74420782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312822-T-C

74420814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312853-G-C

74420814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312853-G-T

74420819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312858-G-T

74420853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312891-C-G

74420920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102312950-C-G

74421073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313055-C-T

74421513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313165-G-A

74421513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313165-G-T

74421524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313175-A-G

74421692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313337-G-A

74422145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313762-C-T

74422207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313820-C-T

74422218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313831-C-T

74422315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313945-T-C

74422315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102313945-T-G

74422369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314000-C-T

74422380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314011-A-G

74422413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314042-C-T

74424792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314205-G-T

http://identifiers.org/hco/3/GRCh38#74424813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102314226-A-C

74424813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314226-A-G

74424897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102314311-C-G

74424900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: synonymous variant
orthologous variants: 102314314-A-G

74424976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314401-A-G

74425629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314690-G-A

74425837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314893-G-A

74425838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314894-G-A

74425849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314905-G-A

74425872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102314924-C-G

http://identifiers.org/hco/3/GRCh38#74426036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102315088-C-A

74426036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315088-C-T

74426140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315195-G-C

74426151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315256-T-C

74426506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315641-G-A

74426710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315862-T-A

74426777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102315929-G-A

74436018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102323904-G-A

74436063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102323943-C-T

74436089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102323969-C-T

74436102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102323977-C-T

74436149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102324024-G-A

74436149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102324024-G-T

74436230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102324107-T-G

74436271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102324148-T-A

http://identifiers.org/hco/3/GRCh38#74436351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102324232-C-A

74436379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102324259-C-G

http://identifiers.org/hco/3/GRCh38#74436494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102324371-A-C

74438014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329563-G-A

74438014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329563-G-T

74438111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329658-A-T

74438291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329825-T-C

74438307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329841-T-C

74438336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329864-T-C

74438358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329888-G-A

74438358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102329888-G-T

74438621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330125-G-A

74438622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330126-G-A

74438671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330176-A-G

74438784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330257-C-T

74438930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330393-T-C

74438972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102330437-T-G

74440346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102333580-A-T

74441179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102333849-T-C

74441213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102333883-A-G

74441348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334018-C-G

74441525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334156-T-C

74441525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334156-T-G

74441534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334165-T-G

74444502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334519-A-T

74444608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102334625-G-T

74445001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335018-C-G

http://identifiers.org/hco/3/GRCh38#74445004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102335021-C-A

74445192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335203-C-T

74445218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335229-C-T

74445228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335239-T-C

74445681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335394-C-T

74445716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335429-C-T

74445728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102335440-A-G

http://identifiers.org/hco/3/GRCh38#74445935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102338047-A-C

74446010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338138-C-T

74446058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338286-G-C

74446141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338396-T-C

74446190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338443-A-T

74446335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338582-G-A

74446335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102338582-G-T

74446421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339456-T-C

74446422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339457-A-G

http://identifiers.org/hco/3/GRCh38#74446481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102339501-A-C

74446482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339502-G-A

74446482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339502-G-T

http://identifiers.org/hco/3/GRCh38#74446699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102339703-C-A

74446699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339703-C-G

74446699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339703-C-T

74446912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339952-T-A

74446912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102339952-T-G

74446987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340025-C-T

74447140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340260-G-C

74447323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340476-T-C

74447573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340736-T-C

74447627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340778-T-C

74447700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340857-A-G

74447852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102340990-T-C

74447973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341108-C-T

74448349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341556-G-A

74448589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341760-A-G

74448673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341844-A-G

http://identifiers.org/hco/3/GRCh38#74448675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102341846-A-C

74448758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341932-C-T

74448794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102341968-A-G

74449556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102343761-T-C

74449560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102343765-T-A

74449655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102343850-A-T

74449680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102343885-T-G

74449810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102344023-A-G

74449877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102344090-G-A

74449982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102344193-T-C

74449987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102344198-T-C

http://identifiers.org/hco/3/GRCh38#74450049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102344249-C-A

74450092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102344285-T-C

http://identifiers.org/hco/3/GRCh38#74456138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102346645-C-A

74456153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346662-G-A

74456157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346666-A-G

74456230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346739-G-A

74456254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346762-A-G

74456362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346860-T-C

74456491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346972-A-G

74456514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102346985-G-A

74456536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347011-C-T

74456621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347094-C-T

74456631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347104-A-T

74456815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347295-C-T

74457037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347516-T-C

74457206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347684-C-T

74457349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347819-G-A

http://identifiers.org/hco/3/GRCh38#74457474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102347950-A-C

74457474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102347950-A-G

74457622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348339-G-C

74457642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348357-G-A

74457647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348364-C-T

74457649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348366-A-G

74457650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348367-C-T

74457690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348414-A-G

74457690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102348414-A-T

74458721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102351156-G-C

74458896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102351318-C-T

74459135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102351525-A-G

74459181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102351569-G-T

74459260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102351618-A-G

74459544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352343-G-C

74459617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352385-C-T

74459655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352425-T-A

74459814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352572-C-T

74460015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352734-G-A

74460015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352734-G-T

74460016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352735-G-A

http://identifiers.org/hco/3/GRCh38#74460047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102352766-C-A

74460074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102352797-A-G

74462372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102365441-C-T

74462740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102365802-G-A

74462831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102365891-C-T

74462882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366178-A-G

http://identifiers.org/hco/3/GRCh38#74463249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102366517-A-C

74463279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366546-C-T

74463286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366553-A-G

http://identifiers.org/hco/3/GRCh38#74463325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102366592-A-C

74463340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366607-G-A

74463397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366666-A-G

74463511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102366769-C-T

http://identifiers.org/hco/3/GRCh38#74463852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102367165-C-A

74463897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367212-G-A

74463951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367258-G-A

74463953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367260-A-G

74463983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367290-G-T

74464070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367376-A-T

74464171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367480-A-G

74464172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367481-C-T

74464216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367521-T-A

74464373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367672-T-A

74464425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367720-T-A

74464425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367720-T-C

http://identifiers.org/hco/3/GRCh38#74464509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102367805-C-A

74464509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102367805-C-T

74465065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368478-C-T

74465068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368481-T-C

74465108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368494-T-C

74465209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368609-A-G

74465273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368669-A-T

74465297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368693-G-A

74465313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368709-G-A

74465341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368738-C-T

74465484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368868-T-C

74465485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368869-T-C

74465485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368869-T-G

74465570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102368961-T-C

74465722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102369098-C-T

74465820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370007-C-T

74465940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370103-T-C

http://identifiers.org/hco/3/GRCh38#74466091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102370242-C-A

74466115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370265-A-G

74466136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370285-T-C

74466244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron_variant, undefined
orthologous variants: 102370362-T-A

74466297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370415-G-A

74466566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370671-G-A

http://identifiers.org/hco/3/GRCh38#74466579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102370684-C-A

74466579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370684-C-T

74466585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370690-G-A

74466585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370690-G-T

74466676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370781-G-A

74466910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102370977-T-A

74466967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371035-T-G

74467139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371175-C-T

74467213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371263-G-T

74467350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371412-A-G

74467673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371740-C-T

74467806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371874-T-C

74467884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102371957-C-T

74467984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372055-T-C

74468050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372122-T-G

http://identifiers.org/hco/3/GRCh38#74468320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102372397-C-A

74468345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372430-G-A

74468393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372460-T-A

74468507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372577-A-G

74468566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372635-C-G

74468566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372635-C-T

74468644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372723-C-T

74468682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372774-A-G

74468748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372839-T-A

74468748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102372839-T-C

74468969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373090-G-A

74469155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373277-C-T

74469376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373469-C-T

74469522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373551-A-G

74469644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373590-A-G

74469679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373599-A-G

74469716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373630-G-C

74469742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373656-T-C

74469912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373788-C-G

74469912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373788-C-T

74469927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373803-T-C

http://identifiers.org/hco/3/GRCh38#74469972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102373853-A-C

74470017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102373905-C-T

http://identifiers.org/hco/3/GRCh38#74471469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102375556-C-A

74471571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102375653-T-C

74471869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102375924-C-G

http://identifiers.org/hco/3/GRCh38#74471964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102376024-C-A

74471985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376045-T-C

74472090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376141-G-T

74472167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376212-C-T

http://identifiers.org/hco/3/GRCh38#74472172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102376217-C-A

74472172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376217-C-G

74472172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376217-C-T

http://identifiers.org/hco/3/GRCh38#74472577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102376648-C-A

74472577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376648-C-T

74472777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102376976-G-A

74472811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377010-T-C

74472932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377133-G-A

74472956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377158-C-G

74473087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377292-C-G

74473185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377367-A-T

74473711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377832-G-A

74473782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102377903-A-T

74473997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102378150-T-A

74473997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102378150-T-C

http://identifiers.org/hco/3/GRCh38#74474329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102378461-C-A

74474329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102378461-C-G

74482579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102388613-G-A

74482747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102388754-G-A

74482819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102388830-C-T

74483008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102395284-C-T

http://identifiers.org/hco/3/GRCh38#74483030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102395309-C-A

74483109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102395386-T-C

74483195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102395474-T-C

74483386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102395628-T-C

74486333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102397088-T-A

74486440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102397198-G-A

74486597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: missense variant
orthologous variants: 102397355-T-C

74486664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102397424-A-T

http://identifiers.org/hco/3/GRCh38#74486706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102397454-C-A

74486706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102397454-C-G

74486706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102397454-C-T

74487079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102398920-C-T

74487112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102398952-C-T

74487321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102399182-G-A

74487382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102399229-G-C

74487382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102399229-G-T

74489784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102404486-C-T

74489901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102404577-T-C

74490075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102404754-C-T

74490332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102405002-G-A

74490383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102405417-C-G

74490675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102405713-C-T

74490900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102405944-G-A

74490905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102405946-A-G

74491477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102406552-G-A

http://identifiers.org/hco/3/GRCh38#74491590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102406685-A-C

74491967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407038-G-A

74492497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407553-G-A

74492497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407553-G-C

74492593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407605-T-C

74492649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407662-C-T

74492759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407767-G-A

74492858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102407885-C-T

http://identifiers.org/hco/3/GRCh38#74494004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102408963-C-A

74494004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102408963-C-T

74494058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102409020-G-A

74494093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102409055-T-A

74494267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102409224-T-A

74495086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102410030-G-T

74495237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102410154-A-G

74495418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102410331-G-A

74495453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102410492-T-C

74495589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102410621-T-G

74496351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102411485-G-T

74496456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102411590-T-A

74496506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102411645-G-T

74496555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102411705-G-T

74496567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102411723-T-C

74496919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102412077-G-A

74497298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102412421-T-C

74497821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102412923-A-G

74498276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102413361-T-A

74498535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102413611-T-C

74498579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102413652-T-C

74498832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102413882-G-A

74498926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102413978-G-A

74499325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414428-C-T

74499478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414600-A-G

http://identifiers.org/hco/3/GRCh38#74499512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102414637-A-C

74499512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414637-A-T

74499545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414670-C-T

74499565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414691-A-G

74499565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414691-A-T

74499580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414705-T-A

74499580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414705-T-C

74499810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414913-A-G

74499823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414926-T-C

http://identifiers.org/hco/3/GRCh38#74499849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102414951-C-A

74499849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102414951-C-T

http://identifiers.org/hco/3/GRCh38#74499924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102415031-C-A

74499998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415103-T-C

74500029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415149-T-C

74500032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415152-C-T

74500117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415243-C-G

74500117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415243-C-T

74500277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415370-A-G

http://identifiers.org/hco/3/GRCh38#74500372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102415461-C-A

http://identifiers.org/hco/3/GRCh38#74500524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102415608-C-A

74500524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415608-C-G

74500527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415611-T-C

74500731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415811-T-A

74500829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102415904-T-C

http://identifiers.org/hco/3/GRCh38#74500857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102415932-C-A

74500941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102416017-G-C

74501074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102416145-C-T

74502917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102417743-G-A

74503105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102417949-G-C

http://identifiers.org/hco/3/GRCh38#74503129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102417973-C-A

74503428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102418272-G-A

74503490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102418335-G-A

74503689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102418527-C-T

74503866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102418709-G-A

74504242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102419100-G-A

http://identifiers.org/hco/3/GRCh38#74505170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102421289-C-A

74505180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102421300-G-T

74505203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102421304-T-C

http://identifiers.org/hco/3/GRCh38#74505496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102421645-C-A

74505678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102421739-T-C

http://identifiers.org/hco/3/GRCh38#74505871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102421942-A-C

http://identifiers.org/hco/3/GRCh38#74506227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102422285-A-C

74506231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102422289-G-T

74506250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102422308-A-G

74506302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102422357-G-C

74506933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102422831-T-C

74506989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102422876-C-T

74509228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102424554-T-C

74509270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102424596-A-G

http://identifiers.org/hco/3/GRCh38#74509720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102424725-A-C

74509780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102424774-G-A

http://identifiers.org/hco/3/GRCh38#74509790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102424780-C-A

74509841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102424833-T-C

74509922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102424912-C-T

74510089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425031-G-A

74510214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425130-C-T

74510305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425218-G-A

74510338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425261-C-G

74510653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425593-T-C

74510718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425655-G-A

74510811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102425735-T-A

74510916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427201-C-G

74510951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427236-T-C

74511182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427420-T-C

74511190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427428-T-A

74511268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427486-A-G

74511298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427514-T-C

74511343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427559-A-G

74511420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427635-T-C

74511693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102427957-C-T

74512034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428298-T-C

74512241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428479-T-C

74512255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428493-T-C

74512286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428524-G-A

74512286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428524-G-C

74512484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428709-T-C

http://identifiers.org/hco/3/GRCh38#74512516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102428727-C-A

74512516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428727-C-T

74512661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428882-G-A

74512661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102428882-G-T

74512819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429013-C-G

74512917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429109-G-A

74512917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429109-G-C

74513397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429574-A-G

74513397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429574-A-T

74513632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429839-T-C

http://identifiers.org/hco/3/GRCh38#74513634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102429841-C-A

74513634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429841-C-T

74513647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429854-A-T

74513756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429999-G-A

74513756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102429999-G-C

74513902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430154-C-T

http://identifiers.org/hco/3/GRCh38#74513966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102430206-C-A

74513966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430206-C-T

74513974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430214-T-C

74514094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430277-G-T

74514154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430327-T-C

74514168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430341-T-A

74514168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430341-T-G

74515524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102430763-T-C

74515834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102431241-C-T

74516000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102431449-A-G

74517602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102432022-C-T

74517610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102432030-A-G

74517631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102432052-A-G

74517917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102432338-C-T

74517997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436420-T-C

74518010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436433-G-A

74518113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436537-G-A

74518113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436537-G-C

74518337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436760-C-T

74518356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436779-G-A

http://identifiers.org/hco/3/GRCh38#74518396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#102436810-A-C

74518454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102436868-T-C

74518667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102437680-T-C

74519531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102439366-G-T

74519986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102439795-A-G

74520148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102439920-G-A

74520210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102439998-T-C

74520328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102440103-A-G

74520418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102440191-A-T

74520434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2173
most severe consequence: intron variant
orthologous variants: 102440207-A-T