74713065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112071880-G-A

74713360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072163-G-A

74713450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072282-A-T

74713477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072309-G-A

74713477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072309-G-T

74713525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072356-G-A

74713525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072356-G-C

74713525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112072356-G-T

74713647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072546-G-A

74713647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072546-G-C

74713647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072546-G-T

74713821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072723-C-T

http://identifiers.org/hco/16/GRCh38#74713894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112072776-C-A

74713894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072776-C-T

74713928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072804-G-A

74713928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072804-G-T

74713966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072862-T-C

74714032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072926-G-A

74714032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072926-G-T

http://identifiers.org/hco/16/GRCh38#74714072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112072954-C-A

74714072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072954-C-T

74714111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112072993-T-G

74714144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 112073028-A-T

74714291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073176-G-A

74714291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073176-G-T

74714307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073195-G-A

74714307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073195-G-T

74714351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073241-G-A

74714351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112073241-G-T

74716277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112074518-G-A

74716277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112074518-G-T

74716280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112074521-C-G

74716280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112074521-C-T

74716411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112074627-C-T

74716567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112074783-G-A

74716567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112074783-G-C

74716567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112074783-G-T

74716658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112074879-A-G

74716658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112074879-A-T

http://identifiers.org/hco/16/GRCh38#74716665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112074886-C-A

74716665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112074886-C-G

74716665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112074886-C-T

http://identifiers.org/hco/16/GRCh38#74716675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112074917-C-A

74716704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112074948-T-G

http://identifiers.org/hco/16/GRCh38#74716718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112074988-C-A

74716897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075113-T-A

74716897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075113-T-C

74716987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075208-C-G

74717080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075252-G-C

74717101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075272-G-A

74717101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112075272-G-C

74717131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112075302-A-G

74717142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112075313-G-A

74717142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112075313-G-T

74718650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075504-A-G

74718650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075504-A-T

74718725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075561-G-A

74718767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075582-A-G

http://identifiers.org/hco/16/GRCh38#74718876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112075726-C-A

http://identifiers.org/hco/16/GRCh38#74718919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112075763-C-A

74718919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075763-C-T

74718932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075776-C-T

http://identifiers.org/hco/16/GRCh38#74718953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112075801-A-C

74718954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112075802-T-C

74719092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 112075940-G-A

74719215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076070-T-A

74719227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076081-T-C

74719227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076081-T-G

http://identifiers.org/hco/16/GRCh38#74719239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112076093-C-A

74719260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076114-G-A

74719260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076114-G-C

74719260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076114-G-T

74719896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076404-C-G

74719900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076408-G-A

74719900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076408-G-T

74720145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112076621-C-G

74723533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112077935-G-A

74724525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112079721-G-A

74724646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112080027-G-A

74725032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112080411-C-G

74725032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112080411-C-T

74725355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112080738-A-G

74725685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081469-G-A

74725691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081475-G-A

http://identifiers.org/hco/16/GRCh38#74725817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112081594-A-C

74725817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081594-A-G

http://identifiers.org/hco/16/GRCh38#74725820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112081597-C-A

74725820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081597-C-T

74725834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081609-T-C

http://identifiers.org/hco/16/GRCh38#74725838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112081613-C-A

74725838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081613-C-T

http://identifiers.org/hco/16/GRCh38#74725909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112081707-C-A

74725909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081707-C-T

74725929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081727-G-A

74725932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112081731-A-G

74725977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081824-T-A

74725977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081824-T-C

74726017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081864-T-G

74726096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081916-A-G

74726102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081922-C-T

74726111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 112081932-T-G

74726197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 112081998-G-A

74726197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 112081998-G-T

74726218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 112082025-G-A

74726218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 112082025-G-T

74726348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082155-A-G

74726349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082156-G-T

74726350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082157-G-A

74726350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082157-G-T

http://identifiers.org/hco/16/GRCh38#74726364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112082171-A-C

74726364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082171-A-G

74726683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082193-G-A

74726683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082193-G-T

74726849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082333-C-G

74726994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082482-T-A

74726994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082482-T-C

http://identifiers.org/hco/16/GRCh38#74727115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112082586-C-A

74727115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082586-C-T

74727215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082681-G-T

http://identifiers.org/hco/16/GRCh38#74727349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112082815-A-C

74727384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 112082850-G-C

74727410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082873-A-G

74727412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082875-G-A

74727446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082898-C-G

74727446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082898-C-T

http://identifiers.org/hco/16/GRCh38#74727510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112082961-C-A

74727510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082961-C-T

74727529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112082971-G-T

74727797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083219-T-C

74727921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083351-C-G

74728323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083629-A-G

74728418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083724-G-A

74728490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083783-G-A

74728514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083809-T-C

74728614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083912-C-T

74728661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112083962-T-G

74730128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112084297-G-A

http://identifiers.org/hco/16/GRCh38#74733231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112086126-C-A

74733231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112086126-C-T

http://identifiers.org/hco/16/GRCh38#74733471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112086958-A-C

74733471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112086958-A-G

74734395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112087484-G-A

74734505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112087581-A-G

74734896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112087931-C-G

74735044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112088102-T-C

74735064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112088124-T-A

74735064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112088124-T-G

74735312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112088393-G-C

74735369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112088449-G-A

74736789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112089303-C-T

74737085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090084-C-G

74737085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090084-C-T

74737266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090268-G-A

74737450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090452-C-T

74737468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090467-C-T

74737628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090609-A-G

74737749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090699-C-G

74737762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090712-G-A

74737934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112090881-G-A

74738275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112091266-G-A

74738444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112091447-G-A

74738940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092044-C-T

74739035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092124-T-G

74739040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092129-G-A

74739070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092170-T-A

http://identifiers.org/hco/16/GRCh38#74739443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112092517-C-A

74739546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092599-G-A

74739566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092605-G-T

74739922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112092956-A-G

74740105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 112093108-T-G

http://identifiers.org/hco/16/GRCh38#74740174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112093183-C-A

74740180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093189-T-G

74740200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093208-A-G

74740768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093400-G-A

74740838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093442-C-T

http://identifiers.org/hco/16/GRCh38#74740987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112093619-C-A

74740987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093619-C-T

http://identifiers.org/hco/16/GRCh38#74741110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112093745-C-A

74741110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093745-C-T

74741135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112093770-A-G

http://identifiers.org/hco/16/GRCh38#74741145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112093780-C-A

74741206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 112093849-G-A

74741257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 112093952-G-A

74741257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 112093952-G-C

74741303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094098-T-C

74741384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094171-T-A

74741390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094177-A-G

74741410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094204-G-T

74741419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094213-T-G

http://identifiers.org/hco/16/GRCh38#74741729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112094573-C-A

74741729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094573-C-G

74741729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094573-C-T

74741912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094829-A-G

74741946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112094862-C-G

74743133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112096073-T-G

74743384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112096413-T-C

http://identifiers.org/hco/16/GRCh38#74743428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112096459-A-C

http://identifiers.org/hco/16/GRCh38#74743431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112096462-C-A

74743431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112096462-C-T

74743508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112096544-G-A

74743711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112096747-G-A

74743711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112096747-G-T

74743928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112096960-G-A

74744099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112097148-A-G

74744099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112097148-A-T

74744280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112097317-C-T

74745010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112097559-G-A

74745455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112098224-G-A

74745733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112098503-C-T

74746550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112099585-T-C

74746590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112099688-T-C

74747506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112100222-C-G

74747506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112100222-C-T

74747651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112100363-T-C

74747804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101033-C-T

74747840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101071-T-G

http://identifiers.org/hco/16/GRCh38#74748054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112101259-C-A

http://identifiers.org/hco/16/GRCh38#74748055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112101260-C-A

74748055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101260-C-G

74748131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101315-G-C

74748315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101552-G-T

74748622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112101836-G-A

74748835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102054-G-A

74749079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102257-C-T

74749105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102282-G-C

74749131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102308-T-C

http://identifiers.org/hco/16/GRCh38#74749380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112102600-A-C

74749400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102641-C-T

74749413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102718-C-T

74749440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102811-A-T

74749476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112102857-G-A

74749879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112103821-G-A

74749923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112103866-C-G

74750040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112103963-G-A

74750271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112104177-G-A

74750271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112104177-G-C

74750561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112104913-C-T

74756185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112107074-T-C

74759159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112110104-G-C

74759235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112110166-C-G

74759389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112110262-T-C

74759553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112110397-T-C

74759906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112110649-C-T

74760420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112111322-G-A

74760509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112111410-T-C

74760597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112111496-C-T

74760686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112111573-C-T

74760735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112111617-G-C

74760796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112111669-T-C

74760874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112111738-A-T

74766814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112114398-G-A

74766984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112114588-G-A

74767126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112114657-T-C

74767126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112114657-T-G

74767217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112114680-G-A

74767893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112115374-G-C

74767959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112115433-A-G

74768155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112115658-T-C

74768501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112115933-C-T

74768654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112116061-A-G

74768930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112116320-G-C

74769696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112117300-A-G

http://identifiers.org/hco/16/GRCh38#74770800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112117854-A-C

74771047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118116-G-A

http://identifiers.org/hco/16/GRCh38#74771727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112118338-C-A

74771953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112118541-T-A

74771953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112118541-T-C

74771981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118553-T-C

74772131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118614-G-A

74772131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118614-G-C

74772178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118660-G-T

http://identifiers.org/hco/16/GRCh38#74772368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112118854-C-A

74772476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118962-G-C

74772476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118962-G-T

74772491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118974-C-T

74772516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112118999-C-G

http://identifiers.org/hco/16/GRCh38#74772519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112119002-A-C

74772528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112119011-C-T

74772570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112119047-T-C

74773907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112119548-A-G

74774073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112119716-T-C

74774395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 112120019-T-C

http://identifiers.org/hco/16/GRCh38#74774397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112120021-C-A

74774417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112120041-G-A

74774417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112120041-G-T

http://identifiers.org/hco/16/GRCh38#74774472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112120100-C-A

74774472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112120100-C-G

74774472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112120100-C-T

74774478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 112120106-G-A

74774478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 112120106-G-C

74774478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 112120106-G-T

http://identifiers.org/hco/16/GRCh38#74774665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112120294-C-A

74774665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 112120294-C-G

74774665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 112120294-C-T

http://identifiers.org/hco/16/GRCh38#74774697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112120326-A-C

74774697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 112120326-A-G

74774697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 112120326-A-T

http://identifiers.org/hco/16/GRCh38#74774798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112120428-C-A

74774798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21197
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112120428-C-T