73958007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84416879-G-T

73958027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84416917-T-A

73958081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84416971-T-C

73958299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417182-G-C

73958546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417412-G-A

73958546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417412-G-C

73958953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417680-G-A

73958953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417680-G-T

73958967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 84417694-G-T

73959039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84417766-T-C

73959250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84417969-C-T

73959495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84418305-A-G

73959495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84418305-A-T

73960858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84418626-A-G

73960934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84418699-G-T

http://identifiers.org/hco/14/GRCh38#73960959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#84418724-C-A

73960959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84418724-C-G

73960959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84418724-C-T

73961118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84418858-T-C

73961284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84419024-G-A

73961284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84419024-G-T

73961343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84419083-T-C

73961506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84419244-C-T

73961637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84419359-G-A

73961637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84419359-G-C

73961637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84419359-G-T

73961951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84419635-T-C

http://identifiers.org/hco/14/GRCh38#73962957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#84420440-A-C

http://identifiers.org/hco/14/GRCh38#73963005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#84420488-C-A

73963005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84420488-C-T

73963029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84420505-G-A

73963043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 84420519-T-C

73963159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84420618-G-A

73963159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84420618-G-C

73963212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84420635-T-C

73963282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84420708-C-T

http://identifiers.org/hco/14/GRCh38#73963284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84420710-C-A

73964067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421448-G-C

73964075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421456-G-A

73964208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421577-A-G

73964316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421696-T-A

73964316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421696-T-C

73964333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84421713-C-T

http://identifiers.org/hco/14/GRCh38#73964650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84422305-C-A

73964650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422305-C-T

http://identifiers.org/hco/14/GRCh38#73964680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84422329-C-A

http://identifiers.org/hco/14/GRCh38#73965762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84422668-C-A

73965762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422668-C-T

73965797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422703-G-A

73965846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422754-G-A

73965861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422769-G-T

73965890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422798-T-C

http://identifiers.org/hco/14/GRCh38#73965900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84422808-C-A

73965900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422808-C-T

73965935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422843-A-G

73965983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84422888-A-G

73966030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423012-T-C

73966125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423107-C-T

73966188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423173-G-T

73966355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423434-A-G

73966378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423464-G-A

73966378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423464-G-T

73966422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423507-T-A

73966422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423507-T-C

73966422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423507-T-G

73966432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423517-T-G

73966437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423526-T-G

73966438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423527-T-C

73966438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423527-T-G

73966494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423579-G-A

73966494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423579-G-T

73966645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423705-G-A

http://identifiers.org/hco/14/GRCh38#73966709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84423769-C-A

73966765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423848-T-C

73966772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423855-G-C

73966772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423855-G-T

http://identifiers.org/hco/14/GRCh38#73966849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84423975-A-C

73966849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84423975-A-T

73966896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84424036-G-T

73967030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424176-A-G

73967047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424193-A-G

http://identifiers.org/hco/14/GRCh38#73967050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84424196-C-A

http://identifiers.org/hco/14/GRCh38#73967157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84424230-C-A

73967157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424230-C-T

73967191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424263-G-C

73967400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424447-T-C

73967539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84424571-G-A

73969876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84425869-T-A

73969876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84425869-T-C

73969976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84425930-G-A

73969990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84425938-T-C

73969999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84425943-C-T

73970052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84425996-C-T

73970067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: missense variant
orthologous variants: 84426011-G-C

73970097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84426041-T-C

http://identifiers.org/hco/14/GRCh38#73970189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84426129-C-A

73970216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84426156-G-T

73970689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84426394-A-G

73970775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84426471-G-T

73971943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427185-C-T

http://identifiers.org/hco/14/GRCh38#73971945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84427186-C-A

73971945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427186-C-G

73971959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427198-T-A

73972051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427335-T-A

73972051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427335-T-C

73972055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427342-T-C

73972075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427369-A-G

73972110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427426-G-A

73972144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427459-C-T

73972179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427489-C-T

73972187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427497-A-G

73972540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84427912-C-T

73972648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84428015-T-C

http://identifiers.org/hco/14/GRCh38#73972759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84428895-C-A

73972759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84428895-C-T

73972856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84428979-T-G

http://identifiers.org/hco/14/GRCh38#73972881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84429003-C-A

73972881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84429003-C-T

73972899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, missense_variant
orthologous variants: 84429021-C-T

73972912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 84429034-A-G

73972993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, missense_variant
orthologous variants: 84429115-T-A

73972993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, missense_variant
orthologous variants: 84429115-T-G

73973083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84429201-C-G

http://identifiers.org/hco/14/GRCh38#73973085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84429203-C-A

73973085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84429203-C-T

73973086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84429204-T-A

73973086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84429204-T-C

73973389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84430298-A-T

http://identifiers.org/hco/14/GRCh38#73973427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84430336-A-C

73973427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84430336-A-G

73973784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84430904-G-A

73973784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84430904-G-T

73973812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84430929-C-T

http://identifiers.org/hco/14/GRCh38#73974010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84431119-A-C

73974010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431119-A-G

73974054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431157-G-T

http://identifiers.org/hco/14/GRCh38#73974070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84431163-C-A

73974070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431163-C-T

73974076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431169-G-T

http://identifiers.org/hco/14/GRCh38#73974117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84431210-A-C

73974407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431458-T-A

73974413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431464-A-G

http://identifiers.org/hco/14/GRCh38#73974499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84431562-C-A

73974541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431609-T-C

73974554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431622-T-C

http://identifiers.org/hco/14/GRCh38#73974903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84431904-A-C

73974903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431904-A-G

73974903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431904-A-T

73974998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431996-G-C

73974998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84431996-G-T

73975054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432050-A-G

73975063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432059-A-T

73975087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432084-G-C

73975087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432084-G-T

73975110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432109-G-A

73975110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432109-G-T

73975122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432119-T-C

http://identifiers.org/hco/14/GRCh38#73975172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84432166-C-A

73975203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432197-G-A

73975228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432216-G-C

73975342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432301-T-C

73975909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432547-A-T

http://identifiers.org/hco/14/GRCh38#73976080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84432715-C-A

73976080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432715-C-T

73976083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432718-C-T

73976206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432811-T-A

73976206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432811-T-C

73976224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432827-G-A

73976224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432827-G-T

73976246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432849-A-G

73976268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432852-C-T

73976271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84432855-C-G

http://identifiers.org/hco/14/GRCh38#73976464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84433045-C-A

73976464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433045-C-T

73976498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433086-G-A

73976498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433086-G-T

73976510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433098-T-C

73976521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433108-T-C

73976560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433147-G-T

73976600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433200-T-G

73976702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433232-T-A

http://identifiers.org/hco/14/GRCh38#73976754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84433266-A-C

73976870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433341-C-T

http://identifiers.org/hco/14/GRCh38#73976886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84433358-C-A

73976886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433358-C-T

73976894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433372-G-A

73976894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433372-G-T

73976978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433464-T-A

73976978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433464-T-C

73976978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433464-T-G

73977011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433497-G-C

73977049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84433537-A-T

73977052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84433540-T-C

73977196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433647-C-G

73977196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433647-C-T

73977212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433666-G-A

73977212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433666-G-T

http://identifiers.org/hco/14/GRCh38#73977269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84433724-C-A

73977269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433724-C-T

http://identifiers.org/hco/14/GRCh38#73977276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84433731-A-C

73977276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433731-A-G

73977279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433734-C-T

73977306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84433761-G-A

73977306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84433761-G-C

73977400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433850-A-G

73977524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433998-T-A

73977524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84433998-T-C

73977735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84434175-G-T

73978077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84434714-T-C

73978078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84434715-G-A

73978129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84434798-G-C

73978141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84434810-A-G

73982923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439106-G-T

http://identifiers.org/hco/14/GRCh38#73982942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439123-C-A

73982942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439123-C-T

73982948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439129-G-A

73982948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439129-G-C

73982948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439129-G-T

http://identifiers.org/hco/14/GRCh38#73982956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439131-C-A

73982956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439131-C-T

http://identifiers.org/hco/14/GRCh38#73983051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439213-C-A

73983090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84439252-G-T

http://identifiers.org/hco/14/GRCh38#73983194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439355-C-A

73983194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439355-C-T

73983216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439373-T-C

73983216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439373-T-G

73983257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439426-G-T

http://identifiers.org/hco/14/GRCh38#73983264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439433-C-A

73983270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439439-G-A

73983270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439439-G-T

73983272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439441-T-C

http://identifiers.org/hco/14/GRCh38#73983289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84439456-C-A

73983289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439456-C-G

73983289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439456-C-T

73983290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84439457-T-C

73984607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84440493-C-T

73984618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84440504-C-T

73984650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84440536-T-C

73986811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84441395-C-T

73986847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 84441431-T-C

http://identifiers.org/hco/14/GRCh38#73986859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84441443-A-C

http://identifiers.org/hco/14/GRCh38#73987009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84441970-A-C

73987009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84441970-A-T

http://identifiers.org/hco/14/GRCh38#73987013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84441974-A-C

73987013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84441974-A-T

73987038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84442005-A-G

73987039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84442006-G-A

73987060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84442035-A-G

73987061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 84442036-G-C

http://identifiers.org/hco/14/GRCh38#73987199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84442261-C-A

http://identifiers.org/hco/14/GRCh38#73987246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84442300-A-C

73987252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442306-A-G

73987252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442306-A-T

73987275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442328-G-A

http://identifiers.org/hco/14/GRCh38#73987279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84442332-C-A

73987279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442332-C-G

73987279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442332-C-T

73987284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442337-G-A

73987284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442337-G-C

73987284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84442337-G-T

73987852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84443419-T-C

73987868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron variant
orthologous variants: 84443435-G-A

73987892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: missense variant
orthologous variants: 84443459-T-C

73988082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: synonymous variant
orthologous variants: 84443646-T-C

http://identifiers.org/hco/14/GRCh38#73988190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84443750-C-A

73988190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443750-C-T

73988202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443761-C-T

73988249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443835-T-C

http://identifiers.org/hco/14/GRCh38#73988255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84443841-C-A

73992138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445623-T-C

http://identifiers.org/hco/14/GRCh38#73992228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84445706-C-A

73992255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445728-C-G

73992255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445728-C-T

73992286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445770-G-A

73992292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445776-T-C

73992295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445779-G-C

73992295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445779-G-T

73993379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84445945-T-C

73993543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446102-T-C

73993636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446196-G-T

http://identifiers.org/hco/14/GRCh38#73993876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84446491-C-A

73993900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446519-G-A

73993900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446519-G-T

73994026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446617-C-T

73994065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446654-C-G

http://identifiers.org/hco/14/GRCh38#73995644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84447078-C-A

73995729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447170-T-C

73995857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447296-A-T

73995967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447464-G-A

73995967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447464-G-T

http://identifiers.org/hco/14/GRCh38#73995969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84447466-C-A

73995969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447466-C-T

http://identifiers.org/hco/14/GRCh38#73995978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84447475-C-A

73995978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447475-C-G

73995978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447475-C-T

73996064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84447562-G-C

73996064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84447562-G-T

73996337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447837-T-C

73996368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447868-G-A

73996368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84447868-G-T

73997059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449291-T-G

73997063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449294-C-T

73997229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449456-G-A

73997231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449458-G-A

73997273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449498-G-C

73997351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449574-T-C

73997468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449697-C-G

73997468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84449697-C-T

74005842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84450165-C-G

74007581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84450546-T-C

74008971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84451424-T-C

74008986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84451434-C-T

74008993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84451441-C-T

http://identifiers.org/hco/14/GRCh38#74009000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84451457-C-A

74009041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84451495-T-C

74009227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84451678-G-T

74009244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84451695-G-T

74009269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84451720-T-C

74015778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452107-G-A

74015778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452107-G-T

74015829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84452157-A-G

http://identifiers.org/hco/14/GRCh38#74015950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84452277-C-A

http://identifiers.org/hco/14/GRCh38#74015956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84452283-C-A

74015999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452322-A-G

74016046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452372-T-A

74016094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452421-T-C

74016238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84452552-C-T

74018629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455149-G-A

74018653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455173-G-A

74018653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455173-G-T

74018701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455215-G-A

74018735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455233-C-T

http://identifiers.org/hco/14/GRCh38#74018751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84455249-C-A

74018771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455293-T-C

74018868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455385-A-T

74018952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455469-G-A

74018952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455469-G-T

74019009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455519-G-A

74019009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455519-G-C

74019009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455519-G-T

74019068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455582-G-A

74019068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455582-G-T

74019096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455633-T-C

74019135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455668-A-G

74019181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455686-C-G

74019181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84455686-C-T

http://identifiers.org/hco/14/GRCh38#74019210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#84455712-C-A

74019210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84455712-C-T

74019328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 84455809-G-A

74019328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 84455809-G-T

74019352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3367
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84455831-C-T