124947773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125492119-A-G

124947886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 125492229-G-T

124947924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125492260-C-G

124947924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125492260-C-T

124947958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125492288-G-A

124947958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125492288-G-T

http://identifiers.org/hco/12/GRCh38#124948062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125492348-C-A

http://identifiers.org/hco/12/GRCh38#124948105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125492386-C-A

124948105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125492386-C-T

124949697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492671-G-A

124949897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492851-G-T

124949901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492855-G-A

124949901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492855-G-T

124949950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492891-T-C

124949950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492891-T-G

124949963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125492904-G-A

124950031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125492975-C-T

124950134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125493073-C-T

124950168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125493107-C-T

124950218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125493157-G-A

124950302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125493240-T-A

124950302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125493240-T-C

http://identifiers.org/hco/12/GRCh38#124950371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125493323-C-A

124950371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125493323-C-G

http://identifiers.org/hco/12/GRCh38#124950417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125493368-C-A

124950417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125493368-C-T

124950522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125493473-G-T

124950638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125493572-C-T

124950684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125493590-C-T

124950783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125493689-C-T

124950793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125493699-G-A

124952407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125494495-G-A

124952407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125494495-G-C

124952407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125494495-G-T

http://identifiers.org/hco/12/GRCh38#124952565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494653-C-A

124952600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494687-G-A

124952600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494687-G-C

124952600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494687-G-T

http://identifiers.org/hco/12/GRCh38#124952612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494699-C-A

124952612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494699-C-G

124952612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494699-C-T

http://identifiers.org/hco/12/GRCh38#124952623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494712-C-A

124952623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494712-C-G

http://identifiers.org/hco/12/GRCh38#124952712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494783-C-A

124952712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494783-C-T

http://identifiers.org/hco/12/GRCh38#124952713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494784-A-C

124952713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494784-A-G

124952713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494784-A-T

http://identifiers.org/hco/12/GRCh38#124952721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125494788-A-C

124952721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494788-A-G

124952765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494798-T-A

124952765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494798-T-C

124952765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494798-T-G

124952768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494801-T-A

124952768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494801-T-C

124952768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494801-T-G

124952798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494828-G-A

124952798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494828-G-C

124952798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125494828-G-T

124952951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 125494900-T-A

124952951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 125494900-T-C

124953203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495017-G-A

124953203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495017-G-T

http://identifiers.org/hco/12/GRCh38#124953267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125495067-C-A

124953267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495067-C-T

124953271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495071-G-A

124953271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495071-G-T

124953403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495171-G-A

124953403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495171-G-C

124953403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495171-G-T

124953474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495207-T-A

124953474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495207-T-C

124953474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495207-T-G

124953492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495225-T-A

124953492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495225-T-C

124953492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495225-T-G

124953555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495267-T-G

124953557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495269-G-A

124953557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495269-G-T

124953565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495277-G-A

124953565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495277-G-T

http://identifiers.org/hco/12/GRCh38#124953577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125495289-A-C

124953577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495289-A-G

124953577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495289-A-T

http://identifiers.org/hco/12/GRCh38#124953628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125495325-A-C

124953628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495325-A-G

124953690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495371-A-G

124953690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495371-A-T

http://identifiers.org/hco/12/GRCh38#124953707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125495388-C-A

124953707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495388-C-G

124953707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495388-C-T

124953738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125495393-A-G

124953884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 125495518-G-A

124953884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 125495518-G-C

124953884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 125495518-G-T

124953974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 125495608-A-G

124953983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 125495617-G-A

124953992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 125495626-G-A

124954078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron variant
orthologous variants: 125495714-G-A

124954178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: synonymous variant
orthologous variants: 125495814-C-T

124956679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125496013-C-T

124956687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125496021-G-A

124956738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496072-G-A

124956762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496096-G-A

124956771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496105-G-A

124956807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496141-G-A

http://identifiers.org/hco/12/GRCh38#124956834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125496168-C-A

124956834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496168-C-G

124956834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496168-C-T

http://identifiers.org/hco/12/GRCh38#124956969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125496254-C-A

124957019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496290-T-C

124957118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125496387-G-A

124957118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125496387-G-T

http://identifiers.org/hco/12/GRCh38#124957174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125496434-C-A

124957174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496434-C-G

124957174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496434-C-T

124957191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496452-G-A

124957191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496452-G-T

124957207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496468-T-A

124957207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496468-T-C

124957241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496509-T-C

http://identifiers.org/hco/12/GRCh38#124957242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125496511-C-A

124957242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496511-C-G

124957242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496511-C-T

124957265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496534-G-T

http://identifiers.org/hco/12/GRCh38#124957282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125496568-C-A

124957282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125496568-C-G

http://identifiers.org/hco/12/GRCh38#124959834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125497634-C-A

124959949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497787-G-C

124959996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497815-G-A

124960024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497840-C-T

124960161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497935-C-G

124960161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497935-C-T

124960175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497949-G-A

124960175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497949-G-C

124960190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497964-C-G

124960190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497964-C-T

124960231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497999-C-G

124960231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125497999-C-T

124960296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125498063-G-A

http://identifiers.org/hco/12/GRCh38#124960452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125498212-C-A

124960452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125498212-C-T

124964609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125499398-C-G

124964609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125499398-C-T

124964683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125499468-A-T

124964821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125499568-G-A

124965180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125499897-G-A

124965252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125499963-C-T

124965310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500020-G-T

124965355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500118-C-T

124965634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500459-T-A

124965634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500459-T-C

124965635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500460-G-A

124965635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500460-G-C

124965650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500473-T-A

http://identifiers.org/hco/12/GRCh38#124965930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125500708-C-A

124965930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500708-C-G

124965930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500708-C-T

124965949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500729-T-C

124965952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500732-T-C

124965952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500732-T-G

http://identifiers.org/hco/12/GRCh38#124966141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125500925-C-A

124966141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125500925-C-T

124966665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501587-G-C

124966671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501593-G-A

124966671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501593-G-T

http://identifiers.org/hco/12/GRCh38#124966747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125501660-C-A

124966747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501660-C-T

http://identifiers.org/hco/12/GRCh38#124966917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125501804-C-A

124966988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125501879-G-A

http://identifiers.org/hco/12/GRCh38#124967042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125501917-C-A

124967042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501917-C-T

124967102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125501979-T-G

http://identifiers.org/hco/12/GRCh38#124967154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125502034-C-A

http://identifiers.org/hco/12/GRCh38#124968598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125502550-C-A

124968598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125502550-C-T

124968653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125502605-G-A

124968705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125502638-G-A

124968705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125502638-G-T

124968721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125502654-C-G

124968733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125502666-A-T

http://identifiers.org/hco/12/GRCh38#124968785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125502696-A-C

124968788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125502699-G-A

124968936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125502805-C-T

124970775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125503274-C-T

124970957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125503447-T-C

http://identifiers.org/hco/12/GRCh38#124971135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125503618-C-A

124971135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125503618-C-T

http://identifiers.org/hco/12/GRCh38#124971287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125503708-C-A

124971287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125503708-C-T

124971344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125503757-G-A

124971368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125503781-G-A

124971418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125503831-G-C

124971418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125503831-G-T

124972409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125504409-G-T

124972605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125504607-T-C

124972605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125504607-T-G

124972646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125504661-G-A

124972646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125504661-G-T

http://identifiers.org/hco/12/GRCh38#124975532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125505491-C-A

124975532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125505491-C-T

124977085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125505988-A-G

124977235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125506118-G-A

124977235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125506118-G-T

124977318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125506204-G-A

124977326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125506212-T-C

124977347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506231-G-A

124977461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506345-G-A

124977461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506345-G-T

124980514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506793-G-A

124980514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506793-G-T

124980547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125506820-G-C

http://identifiers.org/hco/12/GRCh38#124980642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125506936-C-A

124980642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125506936-C-T

124980787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125507054-G-A

124980787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125507054-G-T

124980790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125507057-G-T

http://identifiers.org/hco/12/GRCh38#124980802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125507069-C-A

124980830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125507097-T-C

124980862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507129-G-A

124980862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507129-G-T

http://identifiers.org/hco/12/GRCh38#124980873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125507138-C-A

124980873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507138-C-T

124980898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507166-C-T

http://identifiers.org/hco/12/GRCh38#124980921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125507194-C-A

124980921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507194-C-G

http://identifiers.org/hco/12/GRCh38#124980961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125507233-C-A

124980961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507233-C-T

124981026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125507288-A-G

124982648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508026-T-A

124982648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508026-T-C

124982648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508026-T-G

http://identifiers.org/hco/12/GRCh38#124982665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508057-C-A

http://identifiers.org/hco/12/GRCh38#124982669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508061-C-A

124982669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508061-C-T

124982769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508152-G-A

124982769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508152-G-T

http://identifiers.org/hco/12/GRCh38#124982772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508155-C-A

http://identifiers.org/hco/12/GRCh38#124983082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508398-A-C

124983082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508398-A-G

http://identifiers.org/hco/12/GRCh38#124983094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508410-A-C

124983114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508429-A-G

124986042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508608-C-T

124986047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125508614-C-T

http://identifiers.org/hco/12/GRCh38#124986186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125508751-A-C

124988014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125510348-G-T

124988028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125510362-C-G

124988497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125510730-G-C

http://identifiers.org/hco/12/GRCh38#124988732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125510910-C-A

http://identifiers.org/hco/12/GRCh38#124988806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#125510968-C-A

http://identifiers.org/hco/12/GRCh38#124988930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125511012-C-A

124988930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125511012-C-T

http://identifiers.org/hco/12/GRCh38#124988933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#125511015-C-A

124989099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125511147-G-A

124989099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17210
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 125511147-G-T