http://identifiers.org/hco/3/GRCh38#143972026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94420190-C-A

143972026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94420190-C-G

143972026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94420190-C-T

http://identifiers.org/hco/3/GRCh38#143972217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94420046-C-A

143972217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 94420046-C-G

143972217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 94420046-C-T

143972316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 94419945-G-A

143972316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 94419945-G-C

143972681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419578-G-A

143972681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419578-G-C

143972681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 94419578-G-T

http://identifiers.org/hco/3/GRCh38#143972852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419407-C-A

143972852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419407-C-T

http://identifiers.org/hco/3/GRCh38#143972858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419401-C-A

143972858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419401-C-T

143972882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419377-G-A

143972882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94419377-G-T

http://identifiers.org/hco/3/GRCh38#143972957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419302-C-A

143972957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94419302-C-G

143972957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 94419302-C-T

http://identifiers.org/hco/3/GRCh38#143972969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419290-C-A

143972969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94419290-C-G

143973240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94419248-T-G

http://identifiers.org/hco/3/GRCh38#143973303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419188-C-A

143973303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94419188-C-G

http://identifiers.org/hco/3/GRCh38#143973315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419180-C-A

143973315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94419180-C-G

143973315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94419180-C-T

http://identifiers.org/hco/3/GRCh38#143973319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419176-C-A

143973319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94419176-C-T

143973394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94419125-C-G

143973394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94419125-C-T

http://identifiers.org/hco/3/GRCh38#143973504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94419012-A-C

143973768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418731-G-A

143973768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418731-G-T

http://identifiers.org/hco/3/GRCh38#143973881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94418613-A-C

143973917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418573-C-T

143973931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418559-C-G

143974221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418281-A-G

143974336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418169-T-C

143974371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418133-A-G

143974432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418080-T-C

143974889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417692-T-A

143974903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417689-T-C

143975320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417392-C-T

143975331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417379-G-A

143975332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417378-C-G

143975407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417316-T-C

143976000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416766-T-G

143976025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416742-G-A

143976029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416738-C-T

http://identifiers.org/hco/3/GRCh38#143976359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94416448-C-A

143976359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416448-C-T

143976640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416246-G-A

143976743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416152-T-A

143976886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416015-A-T

143977124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415821-A-G

143977124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415821-A-T

143977322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415614-T-G

143977838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414943-G-A

143978043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414759-A-G

143978182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414637-T-G

143978376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414302-A-T

143978491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94414181-C-T

http://identifiers.org/hco/3/GRCh38#143978608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94414158-A-C

143978608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414158-A-G

143978619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414147-T-G

143978625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414143-T-G

143978631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414137-T-C

143978631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414137-T-G

143978695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414083-T-A

143978695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414083-T-C

143979185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412988-T-C

143979740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94411831-G-C

143980052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94411523-A-G

143980791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94411116-T-C

143980814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94411093-A-G

143984610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94407671-T-G

143984803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94407415-A-G

143984994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94407252-C-T

143985045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94407208-T-C

143985287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406970-G-C

http://identifiers.org/hco/3/GRCh38#143985378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94406892-C-A

http://identifiers.org/hco/3/GRCh38#143985409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94406863-C-A

143985409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406863-C-G

143985409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406863-C-T

143985470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406819-T-C

143985476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406813-G-T

143985478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406811-T-A

143985889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94406401-A-G

143985945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94406355-G-A

143986828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404619-C-T

143986883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404562-C-T

143986944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404498-G-A

143986981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404463-A-G

143987038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404415-C-G

143987155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404308-T-C

http://identifiers.org/hco/3/GRCh38#143988429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94404085-A-C

143988445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404069-C-T

143988523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403984-G-C

143988847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403533-C-G

143988847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403533-C-T

143988862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403518-G-T

143988865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403515-C-T

143989080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403290-A-G

143989155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403152-T-C

143989229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402963-G-A

143989311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402886-C-T

143989369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402835-A-G

143989492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402712-C-T

143989671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94402536-C-T

143989883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94402326-T-A

http://identifiers.org/hco/3/GRCh38#143989975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94402239-A-C

143989978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94402236-G-A

143989978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94402236-G-T

143990020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94402190-G-A

143990020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94402190-G-T

http://identifiers.org/hco/3/GRCh38#143990233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94401992-A-C

143990448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94401793-G-A

143990448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94401793-G-T

http://identifiers.org/hco/3/GRCh38#143990831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94401419-C-A

http://identifiers.org/hco/3/GRCh38#143991026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94401216-C-A

143991026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94401216-C-T

143991156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94401061-A-G

143991351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400884-A-G

143991415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400834-A-T

143991575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400675-A-G

143991633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400613-G-T

143991783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400482-C-T

143991835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400428-T-C

143991843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400420-C-T

http://identifiers.org/hco/3/GRCh38#143991936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94400334-C-A

143991936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400334-C-G

143992221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94400064-G-A

143992434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399866-G-T

143992772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399570-A-T

143993057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399317-G-C

143993214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399274-G-T

http://identifiers.org/hco/3/GRCh38#143993309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94399205-C-A

143993373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399143-G-A

143993575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398957-C-G

143994266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398336-G-T

143994393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398208-G-T

143994470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398135-G-A

143994470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398135-G-C

143994724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397915-A-T

143994725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397914-C-T

143994727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397912-A-G

143994785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397768-A-T

143994957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397602-A-G

143995078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397481-A-G

143995230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397326-C-G

143995251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397305-G-A

143995811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394649-C-T

143995833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394626-G-T

143995852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394607-A-T

143995875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394584-T-A

143995924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394539-A-G

http://identifiers.org/hco/3/GRCh38#143995949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94394515-A-C

143995964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394500-T-A

143996042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394422-G-A

143996107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394356-T-G

143996315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394145-A-T

http://identifiers.org/hco/3/GRCh38#143999070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94390213-A-C

143999116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390169-T-C

143999160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390076-C-G

143999273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389956-A-G

143999374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389859-A-G

143999448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389767-A-G

143999602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389625-G-C

143999994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389302-T-A

144000116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389210-C-T

144000160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389150-A-G

144000982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387758-A-G

144001150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386818-A-G

144001223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386757-A-T

144001225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386755-A-G

144001249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386725-T-C

144001256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386718-A-G

144001792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386458-A-G

http://identifiers.org/hco/3/GRCh38#144004088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94380911-C-A

144004142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380845-A-G

144004144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380843-T-A

144004144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380843-T-C

144004152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380835-A-G

144004829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380467-G-T

http://identifiers.org/hco/3/GRCh38#144004837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94380459-A-C

144004881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380410-A-G

144005193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380106-A-G

144005463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379783-C-T

144005735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379551-T-A

144005772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379510-G-A

144006858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94377240-G-T

144006917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94377194-C-T

144012732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374307-T-C

144013441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373832-C-T

144013903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373411-T-C

http://identifiers.org/hco/3/GRCh38#144013931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94373384-C-A

144013946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373363-A-G

144014113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373198-A-G

144014919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372349-G-A

http://identifiers.org/hco/3/GRCh38#144015462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94371351-C-A

144015462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94371351-C-T

144015885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94371020-A-G

http://identifiers.org/hco/3/GRCh38#144016057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94370877-C-A

144016057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370877-C-G

144016079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370826-G-T

http://identifiers.org/hco/3/GRCh38#144016205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94370694-C-A

144016705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370209-G-A

144016763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370149-A-G

144017115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369279-A-G

144017272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369144-A-G

144017272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369144-A-T

144017298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369120-G-A

144017298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369120-G-T

144017572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368853-G-A

144017631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368816-C-T

144017671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368768-C-T

144018054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368047-A-G

144018400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367645-A-T

144018592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367460-G-T

144018645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367410-C-T

http://identifiers.org/hco/3/GRCh38#144018862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94367193-A-C

144018865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367190-G-A

http://identifiers.org/hco/3/GRCh38#144018899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#94367157-C-A

144018899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94367157-C-G

144018899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94367157-C-T

144030781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94366295-A-T

144031294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365714-C-T

144031596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365440-G-T

144031696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365346-A-G

144031708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365249-A-T

144031886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365050-A-G

144031886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365050-A-T

http://identifiers.org/hco/3/GRCh38#144031993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94364949-C-A

144031993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364949-C-T

144032000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364942-G-A

144032111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364830-C-T

144032192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364758-T-G

144032434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364507-G-A

144032591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364344-T-C

144032650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364288-A-G

144032826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364117-C-G

144032853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364088-A-G

http://identifiers.org/hco/3/GRCh38#144032877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94364064-A-C

144033063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363866-A-G

144033350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363586-T-C

http://identifiers.org/hco/3/GRCh38#144033362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94363574-A-C

144033444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363489-G-A

144033454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363480-C-G

144033454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363480-C-T

144033495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363439-C-T

144033564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363364-T-G

144033581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363347-A-G

144033620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363308-T-C

144033639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363289-A-G

144033711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363224-G-A

http://identifiers.org/hco/3/GRCh38#144033769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94363171-C-A

144033769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363171-C-G

144033866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363070-C-G

http://identifiers.org/hco/3/GRCh38#144033909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94363016-A-C

144034239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362719-C-G

144034324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362642-G-A

144034405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362558-G-T

http://identifiers.org/hco/3/GRCh38#144034477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94362435-C-A

http://identifiers.org/hco/3/GRCh38#144034478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94362434-C-A

144034478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362434-C-T

144034590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: non coding transcript exon variant
orthologous variants: 94362309-A-G

144034648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: non coding transcript exon variant
orthologous variants: 94362273-T-C

144034688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94362238-G-T

144034703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362225-A-G

144034717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362211-A-G

144034816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362108-C-G

144034848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362076-A-G

144034849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362075-T-A

144035414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361506-T-A

144035526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361382-G-T

144035542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361366-C-T

144035554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361350-G-A

144035573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361315-G-A

http://identifiers.org/hco/3/GRCh38#144035585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94361303-C-A

144035716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360912-G-C

144035793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360834-A-G

144035843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360784-C-G

144035891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360738-A-T

144035947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360683-T-A

144036012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360615-G-T

144036096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360532-G-A

144036691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359235-G-A

144037329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358814-G-C

144037555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358609-T-G

144037779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358394-A-G

144037968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358218-A-G

144037979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358207-A-G

144038100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358148-A-G

144038100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358148-A-T

144038277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357976-T-C

144038518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357508-A-G

144038526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357500-G-A

144038642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357384-C-T

144038965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357051-G-T

144039000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357014-G-A

144039000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357014-G-T

144039049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356970-A-G

144039563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356650-A-G

144039587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356619-T-C

144039681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356511-C-T

144039897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356278-T-A

144040025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356162-C-T

144040104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355922-G-A

144040490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355512-A-G

144040560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355454-T-C

144040569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355449-G-A

144040569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355449-G-T

144040588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355430-G-A

144040721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355323-A-T

144041013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355050-C-G

144041013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355050-C-T

144041130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354948-A-G

144041337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354738-A-G

144041339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354736-T-A

144041382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354697-A-G

144041583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354331-T-G

144041751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354169-G-A

144042715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353281-A-G

144042821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353183-T-A

144042856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353149-A-G

144043181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352853-A-G

144044344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352132-A-T

144044349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352127-A-G

144044436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352061-T-C

144044515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351982-A-G

144044783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351756-T-G

http://identifiers.org/hco/3/GRCh38#144044852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94351662-A-C

144044889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351618-T-C

144045315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350516-G-A

144045315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350516-G-C

144047097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347089-G-C

http://identifiers.org/hco/3/GRCh38#144047479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94346596-C-A

144047643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94346432-C-T

144048540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345740-A-G

144048552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345736-C-G

144048552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345736-C-T

144048591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345697-A-G

http://identifiers.org/hco/3/GRCh38#144048660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28490
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#94345599-C-A