101420576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49535565-C-T

101420887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536015-T-C

101420966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536092-A-G

http://identifiers.org/hco/9/GRCh38#101421252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536312-C-A

101421252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536312-C-T

101421256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536316-G-T

http://identifiers.org/hco/9/GRCh38#101421264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536324-A-C

101421264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536324-A-G

http://identifiers.org/hco/9/GRCh38#101421276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536336-C-A

101421276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536336-C-T

101421280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536340-A-G

http://identifiers.org/hco/9/GRCh38#101421296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536351-C-A

101421296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536351-C-T

101421309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536364-G-A

101421309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536364-G-T

http://identifiers.org/hco/9/GRCh38#101421327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536382-C-A

101421353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: 49536403-G-C

http://identifiers.org/hco/9/GRCh38#101421400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49536448-C-A

101421857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: synonymous variant
orthologous variants: 49536841-A-G

101421890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: synonymous_variant, undefined
orthologous variants: 49536874-C-T

101421927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49536911-G-A

101421956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: 49536941-C-G

101421956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: 49536941-C-T

101422036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: 49537022-A-G

http://identifiers.org/hco/9/GRCh38#101422049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#49537035-C-A

101422049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: 49537035-C-G

101423773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49537234-G-C

http://identifiers.org/hco/9/GRCh38#101423790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49537251-A-C

http://identifiers.org/hco/9/GRCh38#101423828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49537288-C-A

101423840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49537300-G-T

101424002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49537463-T-G

101424015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49537476-G-A

101424464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49537768-C-T

101424675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49537985-C-T

101424734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49538043-C-G

101424734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49538043-C-T

101425057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538342-G-A

101425141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538412-T-A

101425307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538563-G-T

101425339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538596-G-T

101425362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538623-A-G

http://identifiers.org/hco/9/GRCh38#101425381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49538642-C-A

101425396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538657-T-C

101425441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49538706-A-T

101425477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense variant
orthologous variants: 49538742-G-A

101425477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense variant
orthologous variants: 49538742-G-C

101425570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49538835-G-C

101425570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49538835-G-T

101425595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49538860-G-A

101425595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49538860-G-T

101425639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538904-G-A

101425682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538945-T-C

101425682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538945-T-G

101425748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539011-G-A

101425748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539011-G-T

http://identifiers.org/hco/9/GRCh38#101425762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49539022-C-A

101425783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539043-T-C

101425846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539098-G-A

101425959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539198-T-G

http://identifiers.org/hco/9/GRCh38#101425966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49539205-A-C

101425983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539221-C-T

101426385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539547-T-A

http://identifiers.org/hco/9/GRCh38#101426389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49539551-C-A

http://identifiers.org/hco/9/GRCh38#101426679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49539838-C-A

101426687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539846-T-C

101426696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539855-T-C

101426869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540120-C-T

101426934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540182-A-T

101426957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540193-C-G

101427080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540320-C-T

101427515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49541164-G-A

101427515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49541164-G-T

http://identifiers.org/hco/9/GRCh38#101427596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49541245-A-C

101427596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49541245-A-G

101427623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49541272-C-T

101427626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49541275-T-C

http://identifiers.org/hco/9/GRCh38#101427694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49541347-A-C

101427694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541347-A-G

101427694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541347-A-T

101427698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541351-G-T

101427711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541365-G-T

101427769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541408-G-A

101427769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541408-G-T

101427774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541413-G-A

101427774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541413-G-T

101427783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541422-C-T

101427837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541475-A-T

101427847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541483-T-C

101428186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541791-G-T

101428420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542743-A-G

101428435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542758-T-G

http://identifiers.org/hco/9/GRCh38#101428463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49542788-C-A

101428473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49542798-A-G

101428494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49542819-T-C

101428503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49542828-A-G

101428503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49542828-A-T

101428534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542858-A-T

101428543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542867-A-G

http://identifiers.org/hco/9/GRCh38#101428552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49542876-A-C

101428552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542876-A-G

http://identifiers.org/hco/9/GRCh38#101428664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49542970-C-A

http://identifiers.org/hco/9/GRCh38#101428965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49543213-A-C

101429579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543501-G-T

101429652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543565-A-G

101429693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543596-G-A

101429693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543596-G-T

101429750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543652-T-A

101429791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49543693-G-C

101429913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49543815-G-A

101429913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49543815-G-C

101429913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49543815-G-T

http://identifiers.org/hco/9/GRCh38#101429923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49543825-A-C

101430001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543905-A-G

101430013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543917-T-C

101430071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543971-T-C

101430106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544018-T-A

101430166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544078-G-A

101430224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544129-G-A

101430279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544214-T-C

http://identifiers.org/hco/9/GRCh38#101430284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49544222-A-C

101430570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544608-T-A

101430570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544608-T-C

101430698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544716-T-C

101430719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544744-G-A

101430719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544744-G-T

101430737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544760-A-G

101430754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544777-T-C

101430754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544777-T-G

101430824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49544845-T-C

101430914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49544942-G-A

101430928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49544956-G-A

101430928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49544956-G-T

http://identifiers.org/hco/9/GRCh38#101430958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49544986-C-A

101430958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49544986-C-G

101430958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49544986-C-T

http://identifiers.org/hco/9/GRCh38#101431036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49545050-A-C

101431036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49545050-A-T

101431060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49545074-C-T

101431119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49545156-C-T

101431444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49545423-G-A

101431446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49545425-G-A

101432468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49546041-G-A

101432642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49546208-A-G

101432687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49546254-C-T

101432828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49546786-A-G

101432847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49546804-C-T

101433444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49547398-C-T

101434237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548139-G-A

101434252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548154-G-A

101434303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548186-G-T

101434307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548190-G-A

101434422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548295-A-G

101434425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548298-A-G

101434440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548315-G-T

101434592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548469-G-A

101434791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548616-C-T

101434818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548627-C-T

101435017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49548807-C-T

101435241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49549014-T-C

http://identifiers.org/hco/9/GRCh38#101435319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49549090-A-C

http://identifiers.org/hco/9/GRCh38#101435616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49549344-C-A

http://identifiers.org/hco/9/GRCh38#101435629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49549357-C-A

http://identifiers.org/hco/9/GRCh38#101435668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49549394-C-A

101435718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49549443-G-A

101435718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49549443-G-C

http://identifiers.org/hco/9/GRCh38#101435830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49549561-C-A

101435830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49549561-C-T

101436262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49549982-C-T

101436304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49550024-C-G

101436661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49551927-C-T

http://identifiers.org/hco/9/GRCh38#101436837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49552258-C-A

101436924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49552345-G-T

101437263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49552772-G-A

101437380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49552879-T-C

http://identifiers.org/hco/9/GRCh38#101437459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49552963-C-A

101437494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49552998-T-C

101437651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553141-G-T

101437685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553174-T-C

101437715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553218-A-G

101437812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553345-C-T

101437813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553346-T-C

101437887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553407-C-T

101437956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, undefined
orthologous variants: 49553478-C-T

101437992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553514-T-C

101438018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553540-G-A

101438028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553548-G-A

101438244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553764-C-G

101438245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553765-T-C

101438261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553781-G-A

101438269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553789-G-C

101438326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49553927-A-G

101438578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49554882-T-A

http://identifiers.org/hco/9/GRCh38#101438628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49554924-C-A

101438809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555054-G-A

101438923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555169-A-G

101438995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555228-T-C

101439017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555250-C-G

101439017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555250-C-T

http://identifiers.org/hco/9/GRCh38#101439032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49555266-A-C

101439320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555639-G-A

101439414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555743-A-T

101439680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49555978-A-G

http://identifiers.org/hco/9/GRCh38#101439972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49556249-A-C

101440133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49556436-C-G

101440133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49556436-C-T

101440685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558092-G-T

101440772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558181-A-G

101440794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558202-T-C

101441185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558561-G-A

101441265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558639-C-T

101441269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558643-G-A

101441276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558650-A-G

101441309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558698-C-T

101441318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558703-C-T

101441383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558769-A-T

101441435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron variant
orthologous variants: 49558826-G-A

101442235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49558996-G-C

101442244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49559005-G-A

101442258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49559019-T-C

101442314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49559076-T-C

101442586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49559248-T-C

101442765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49559315-A-G

101443016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559522-G-A

101443061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559570-T-G

101443233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559765-A-G

101443233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559765-A-T

http://identifiers.org/hco/9/GRCh38#101443339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49559869-C-A

101443339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559869-C-T

101443393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49559937-C-G

http://identifiers.org/hco/9/GRCh38#101443501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#49560042-C-A

101443632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560164-T-G

101443735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560277-C-G

101443735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560277-C-T

101444589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560541-C-T

101444634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560569-G-A

101444657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560592-G-A

101444769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560696-T-C

101444769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49560696-T-G

101445418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49560903-C-G

101445528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49561021-A-G

101445583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49561070-C-T

101445713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49561174-G-A

101445823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49561292-C-T