48727558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317455-T-C

48727578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317431-T-A

48727608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317401-G-T

http://identifiers.org/hco/1/GRCh38#48727662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111317352-C-A

48727662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317352-C-T

http://identifiers.org/hco/1/GRCh38#48727663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111317351-C-A

48727663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317351-C-G

48727695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317317-T-C

48727725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317272-T-A

48727725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317272-T-C

48727725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317272-T-G

http://identifiers.org/hco/1/GRCh38#48727752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111317240-C-A

48727752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111317240-C-T

48728056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316932-A-G

48728114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316875-A-G

48728133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316856-C-T

http://identifiers.org/hco/1/GRCh38#48728149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111316841-C-A

48728188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316801-A-G

48729403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316265-T-C

48729577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316131-C-T

48729720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315996-G-T

48729845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315898-C-T

48730168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315630-A-G

48730439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315429-T-A

48730836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315074-C-T

48731193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314728-G-A

48731924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314118-T-C

48732086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314032-G-T

48732123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313994-G-C

48732220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313904-A-G

48733939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313527-T-G

48733991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313488-A-G

48734261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313190-T-C

48734356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313091-C-T

48734357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313090-A-G

48734375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313075-A-G

48734401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313049-T-C

48734460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313015-G-A

48734461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313014-T-C

48734725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312767-C-G

48734846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312637-C-T

48734898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312579-T-G

48734919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312558-G-A

http://identifiers.org/hco/1/GRCh38#48735056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111312444-A-C

http://identifiers.org/hco/1/GRCh38#48735157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111312363-A-C

48735167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312353-C-T

48735198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312326-A-G

48735293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312241-G-A

48735381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312165-G-A

48735438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312136-G-T

48736136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311597-G-T

http://identifiers.org/hco/1/GRCh38#48736176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111311556-A-C

48736190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311542-A-G

http://identifiers.org/hco/1/GRCh38#48736192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111311540-A-C

48736193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311539-G-A

48736193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311539-G-C

48736250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111311482-C-T

48736521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311213-T-C

http://identifiers.org/hco/1/GRCh38#48736543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111311193-C-A

48736543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311193-C-T

48736562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311174-T-A

48736562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311174-T-C

48736601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311163-G-A

48736601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311163-G-T

48736700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311081-T-C

48736785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311006-G-C

48736983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310829-T-A

48738001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310108-T-A

48738001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310108-T-C

48738028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310082-C-T

48738389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309690-C-G

48738389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309690-C-T

http://identifiers.org/hco/1/GRCh38#48738834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111309288-A-C

http://identifiers.org/hco/1/GRCh38#48739054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111309069-C-A

48739093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309031-T-G

48739228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308896-T-C

48739767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308459-T-C

48739767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308459-T-G

48739869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308351-T-G

48739967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308249-G-C

48740052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308163-T-C

48740263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307948-T-A

48740263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307948-T-C

48740627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307591-T-C

48740706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307518-C-T

48740749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307475-G-A

48741142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307121-T-C

48741207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307057-C-T

48741301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306962-C-T

48741310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306954-C-G

48741480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306804-G-A

http://identifiers.org/hco/1/GRCh38#48741583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111306715-C-A

48741712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306597-A-G

48742517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305958-A-G

48742813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305659-A-G

http://identifiers.org/hco/1/GRCh38#48743178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111305309-C-A

48743178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305309-C-T

48743179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305308-G-A

48743225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305262-G-T

48743363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305125-A-G

48743396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305093-A-T

48743619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304897-T-C

48743619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304897-T-G

48743750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304789-C-T

48743951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304597-A-G

48744084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304466-G-A

48744112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304438-G-C

48744452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304135-T-C

48744904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303683-A-G

48744904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303683-A-T

48745097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303525-T-A

48745343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303290-T-G

48745802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302963-T-C

48746166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302581-T-C

48746185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302562-G-A

48746227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302464-T-A

48746271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302430-C-T

48746556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302186-C-T

48746665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302089-G-A

48746991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301757-G-T

48747466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301261-G-A

48747856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111300920-T-C

48748014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111300836-T-C

48748555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111300295-G-A

48748555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111300295-G-T

48748771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111300095-T-C

48748886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299986-C-T

48748981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299896-C-T

48751523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299199-C-G

48751669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299050-A-T

48751803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298983-T-C

http://identifiers.org/hco/1/GRCh38#48752424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111298409-A-C

48752425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298408-T-C

48752612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298224-A-G

48752673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298167-T-C

48752963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298063-T-C

48753941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297230-C-G

48753976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297196-A-G

48753986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297185-T-A

48754247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111295298-G-A

48754357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111295192-T-A

48754521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111295030-C-G

48754687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294906-T-C

48754730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294830-C-G

48754980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294659-C-T

48755025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294608-G-A

48755089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294540-G-A

48755372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294279-T-C

48755408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294229-C-T

http://identifiers.org/hco/1/GRCh38#48755967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111293756-A-C

48756174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293545-T-G

48756478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293160-C-T

48756736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292905-A-G

http://identifiers.org/hco/1/GRCh38#48756801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111292842-C-A

48757002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292641-T-C

48757131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292426-G-A

48757167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292388-G-A

48757686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291961-G-T

48757891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291767-G-T

48757924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291730-T-G

48758190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291418-T-A

48758398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291228-A-G

48758669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290983-G-C

48758703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290946-T-G

48758842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290810-G-T

48759558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290103-C-G

48759662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289999-T-C

http://identifiers.org/hco/1/GRCh38#48759944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111289740-A-C

http://identifiers.org/hco/1/GRCh38#48760031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111289659-C-A

48760074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289609-C-G

48760102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289583-A-G

http://identifiers.org/hco/1/GRCh38#48760184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111289492-C-A

48760184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289492-C-T

48760509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289200-T-C

48760544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289179-G-A

48760551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289172-T-C

48760580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289143-T-C

http://identifiers.org/hco/1/GRCh38#48760946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111288744-C-A

48761025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288662-A-T

http://identifiers.org/hco/1/GRCh38#48761062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111288625-C-A

http://identifiers.org/hco/1/GRCh38#48761118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111288571-C-A

http://identifiers.org/hco/1/GRCh38#48761217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111288464-C-A

48761217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111288464-C-G

http://identifiers.org/hco/1/GRCh38#48761549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111288145-A-C

48761549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288145-A-G

48761619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288075-T-C

48761644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288051-T-C

48761675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288025-A-G

48761709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287991-G-A

48762102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287407-G-A

48762286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287233-A-G

48762533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286987-C-T

48762579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286930-G-A

48762898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286644-T-C

http://identifiers.org/hco/1/GRCh38#48762928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111286614-A-C

48762980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286569-C-G

http://identifiers.org/hco/1/GRCh38#48763078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111286471-A-C

48763276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286297-T-A

48763427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286144-A-G

48763649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285785-T-A

48763698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285738-T-C

48763868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285584-G-C

http://identifiers.org/hco/1/GRCh38#48763879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111285573-A-C

48763879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285573-A-T

48764056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285394-C-G

48764105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285345-G-A

48764661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284843-A-G

48765082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284486-C-T

48765104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284463-T-A

48765298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284269-C-G

48765377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284192-T-C

48765411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284150-G-C

48765590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283990-A-T

http://identifiers.org/hco/1/GRCh38#48765710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111283877-C-A

http://identifiers.org/hco/1/GRCh38#48766024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111283626-A-C

48766039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283611-C-T

48766366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282745-C-T

http://identifiers.org/hco/1/GRCh38#48766574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111282535-C-A

http://identifiers.org/hco/1/GRCh38#48766668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111282445-C-A

48767039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282079-T-C

48767082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282032-T-C

48767122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282006-T-C

http://identifiers.org/hco/1/GRCh38#48767151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111281964-C-A

48767712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111281404-T-C

48767830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111281295-C-T

48767843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111281282-A-T

http://identifiers.org/hco/1/GRCh38#48768050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111281121-C-A

48768091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111281081-T-A

48768091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111281081-T-C

48768357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280837-C-T

48768417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280766-G-C

48768447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280757-T-C

48768558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280681-C-T

48768815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280393-C-T

48769069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280156-T-G

48769216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111280039-C-T

48769434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279857-T-C

http://identifiers.org/hco/1/GRCh38#48769572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111279768-A-C

48769574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279766-T-A

48769666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279681-T-C

48769730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279625-C-T

48769826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279521-G-T

48770055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279328-C-G

48770107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279275-C-T

http://identifiers.org/hco/1/GRCh38#48770327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111279060-C-A

48770688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111278713-C-G

48770737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111278662-C-T

48771018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111278238-T-C

48771067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111278203-A-G

48771374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277901-A-G

48771598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277624-G-A

48771966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277242-A-G

48772019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277178-T-C

48772031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277138-C-G

48772336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276869-G-A

48772523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276707-T-C

48772543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276688-A-G

48772583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276646-G-T

http://identifiers.org/hco/1/GRCh38#48772960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111276317-C-A

48772960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276317-C-T

http://identifiers.org/hco/1/GRCh38#48773044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111276237-A-C

48773081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111276203-G-A

48773353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275953-C-T

48773789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275528-G-A

48773913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275388-T-C

48774054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275182-G-C

48774068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275168-T-G

48774228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275011-C-T

48774229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111275010-C-T

48774406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111274753-A-G

48774718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111274396-C-T

48774821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111274300-T-G

48774861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111274261-C-G

48774952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111274184-T-A

48775479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111273641-T-A

48775766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111273366-C-T

48775877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111273249-C-T

48776208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272976-A-G

48776342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272841-G-A

48776438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272750-C-T

http://identifiers.org/hco/1/GRCh38#48776479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272710-A-C

48776488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272701-G-A

http://identifiers.org/hco/1/GRCh38#48776493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272696-C-A

48776493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272696-C-T

48776494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272695-A-G

http://identifiers.org/hco/1/GRCh38#48776527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272668-C-A

48776527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272668-C-T

http://identifiers.org/hco/1/GRCh38#48776569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272631-C-A

48776569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272631-C-T

http://identifiers.org/hco/1/GRCh38#48776611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272590-A-C

48776611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111272590-A-G

48776611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111272590-A-T

http://identifiers.org/hco/1/GRCh38#48776643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272558-C-A

48776643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111272558-C-T

48776755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111272446-G-A

http://identifiers.org/hco/1/GRCh38#48776865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#111272339-C-A

48776895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111272310-G-A

48776895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25668
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111272310-G-T