141051592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900650-G-A

http://identifiers.org/hco/3/GRCh38#141051667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96900575-C-A

141051695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900547-C-T

141051754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900483-G-A

141051754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900483-G-C

141051754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900483-G-T

http://identifiers.org/hco/3/GRCh38#141051876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96900361-C-A

141051876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900361-C-T

http://identifiers.org/hco/3/GRCh38#141051912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96900325-C-A

141051912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900325-C-T

141051917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96900320-G-T

http://identifiers.org/hco/3/GRCh38#141051927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96900310-C-A

141052494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96899785-T-A

141052494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96899785-T-C

141052957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96899404-C-T

141053207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96898977-T-C

141053207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96898977-T-G

http://identifiers.org/hco/3/GRCh38#141053855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96898227-A-C

141053855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96898227-A-T

141054169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96897959-C-G

141054202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96897920-C-G

141054202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96897920-C-T

141054621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96897495-C-T

141054662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96897454-C-T

http://identifiers.org/hco/3/GRCh38#141055742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96896469-C-A

141055742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96896469-C-T

141055937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96896305-G-C

141056056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96896206-G-A

141056117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96896172-C-T

141056129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96896161-C-G

141056385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96895959-C-T

141056414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96895918-T-C

141056918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96895433-A-G

141057129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96895217-C-T

141057403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894955-T-C

141057507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894926-G-A

141057758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894430-G-T

141057832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894377-T-C

141057901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894308-T-C

141057921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894287-C-G

141057921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894287-C-T

141058052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96894160-A-G

141058413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893823-T-C

141058457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893779-G-A

141058843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893433-A-G

141058961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893324-C-T

141059045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893247-A-T

141059172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96893194-C-G

141059872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892699-G-A

141060130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892463-T-C

141060191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892422-C-T

141060404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892262-T-A

http://identifiers.org/hco/3/GRCh38#141060478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96892199-C-A

141060484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892193-C-T

141060487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96892189-C-T

141062699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96886119-A-T

141062754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96886071-T-C

http://identifiers.org/hco/3/GRCh38#141062756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96886069-A-C

http://identifiers.org/hco/3/GRCh38#141062857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96885973-A-C

141062919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96885909-T-C

http://identifiers.org/hco/3/GRCh38#141063106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96885734-A-C

141063615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96885239-C-T

http://identifiers.org/hco/3/GRCh38#141064081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96884371-C-A

141064340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96884113-G-A

141064340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96884113-G-C

141064436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96884016-G-A

141064657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96879587-G-A

141064813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96879413-C-T

141065042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96879187-T-C

141065133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96879108-G-T

141065194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96879069-C-T

141065343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96878928-C-T

141065878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96878529-T-A

141065878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96878529-T-C

141065878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96878529-T-G

141066012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96878412-G-C

141066183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878241-C-G

141066183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878241-C-T

141066276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878148-C-T

141066312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878112-G-A

141066312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878112-G-T

http://identifiers.org/hco/3/GRCh38#141066333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96878091-C-A

141066333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878091-C-G

141066333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878091-C-T

http://identifiers.org/hco/3/GRCh38#141066339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96878085-C-A

141066339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878085-C-T

http://identifiers.org/hco/3/GRCh38#141066396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96878028-C-A

141066396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96878028-C-T

http://identifiers.org/hco/3/GRCh38#141066438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96877986-C-A

http://identifiers.org/hco/3/GRCh38#141066465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96877959-C-A

141066465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96877959-C-G

141066465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96877959-C-T

http://identifiers.org/hco/3/GRCh38#141066771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96877653-A-C

141066771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96877653-A-G

http://identifiers.org/hco/3/GRCh38#141066854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96877572-A-C

141066854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877572-A-G

http://identifiers.org/hco/3/GRCh38#141066861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96877549-C-A

141066861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877549-C-T

141066886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877527-G-A

141066886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877527-G-T

141066921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877493-T-A

141066921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877493-T-C

141066934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877480-T-A

141066934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877480-T-C

141067096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877357-G-C

141067096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877357-G-T

141067217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877272-C-G

141067268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877225-G-C

141067388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877108-A-G

141067436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877054-C-T

141067437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877053-A-G

141067438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96877052-A-G

141067820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96876363-C-T

141067950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96876210-C-G

141068448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875747-C-T

141068463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875738-T-A

141068623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875594-A-G

141068676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875555-C-T

141068702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875532-G-A

141068762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96875477-C-T

141069567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96874831-T-C

141069567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96874831-T-G

http://identifiers.org/hco/3/GRCh38#141069690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96874797-A-C

141069748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96874744-A-G

http://identifiers.org/hco/3/GRCh38#141069830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96874656-A-C

141070851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96874018-C-G

141070893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96873977-A-G

141071090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96873822-A-T

141071109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96873803-T-C

141071223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96873695-C-T

141071237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96873681-T-A

141071727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96873554-A-G

141071759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96873514-C-T

141072996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872735-G-A

141072996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872735-G-T

141073098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872633-T-C

141073107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872624-C-T

141073236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872501-C-T

141073491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96872257-A-G

141073722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96871959-T-A

141073976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96871672-G-A

141074160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96871484-A-G

141074443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96871223-G-A

141074660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96871019-C-T

141075012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870765-G-C

141075073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870705-T-A

http://identifiers.org/hco/3/GRCh38#141075074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96870704-C-A

141075085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870693-A-G

141075110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870672-T-G

141075153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870620-C-T

141075166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870606-T-G

141075543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870239-G-T

141075605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870208-G-A

141075686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870117-G-T

141075705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870096-C-T

141075709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96870092-C-T

141076656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96869685-T-C

141076659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96869682-G-A

141076659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96869682-G-C

141076659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96869682-G-T

141076793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96869582-A-G

141077066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869306-G-A

141077066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869306-G-T

141077112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869260-T-C

141077152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869221-C-G

141077152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869221-C-T

http://identifiers.org/hco/3/GRCh38#141077232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96869142-C-A

141077232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96869142-C-T

141077457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96868881-A-G

http://identifiers.org/hco/3/GRCh38#141077496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96868697-C-A

141077496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96868697-C-T

http://identifiers.org/hco/3/GRCh38#141077599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96868539-C-A

141077599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868539-C-T

141077617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868521-G-A

141077617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868521-G-T

141077667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868471-G-A

141077766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868422-A-G

141077845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868343-A-G

141077998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868181-G-T

141078167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96868039-G-C

141078263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867948-G-A

141078398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867819-G-C

141078472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867770-G-A

141078577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867697-G-A

141078723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867561-G-C

141079537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96867044-C-T

141079580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866991-C-T

141079807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866753-G-A

141080182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866436-G-T

141080184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866434-T-A

141080187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866431-T-C

141080187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866431-T-G

141080234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96866388-T-A

141080285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96866337-T-C

http://identifiers.org/hco/3/GRCh38#141080286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96866336-C-A

141080446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866192-T-C

http://identifiers.org/hco/3/GRCh38#141080458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96866180-C-A

http://identifiers.org/hco/3/GRCh38#141080462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96866176-C-A

141080462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866176-C-T

http://identifiers.org/hco/3/GRCh38#141080473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96866165-C-A

141080473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866165-C-T

141080477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866158-T-G

141080538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866132-T-A

141080538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866132-T-C

http://identifiers.org/hco/3/GRCh38#141080543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96866127-C-A

141080543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866127-C-G

141080579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96866092-C-G

141080700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96865981-C-G

141081119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96865589-A-G

141081197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96865553-T-G

141082002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864857-C-T

141082159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864655-G-A

141082262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864534-G-A

141082262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864534-G-T

141082396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864416-T-C

141082500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864322-T-C

141082562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864298-G-A

141082846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864175-C-T

141082919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96864148-C-T

141083321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863960-A-T

141083425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863863-G-C

http://identifiers.org/hco/3/GRCh38#141083844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96863502-C-A

141083893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863466-C-G

141084058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863334-G-A

141084279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863125-G-A

141084300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863092-C-T

http://identifiers.org/hco/3/GRCh38#141084310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96863082-C-A

141084310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96863082-C-G

141084759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96862670-C-T

141084969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96862497-G-A

141084969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96862497-G-T

141085065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96862266-T-C

141085185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96862152-G-A

http://identifiers.org/hco/3/GRCh38#141085335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96862010-A-C

http://identifiers.org/hco/3/GRCh38#141087842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96861951-C-A

141088100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96861707-G-A

141088682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96860657-A-T

141089699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96859701-G-A

141090424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857553-G-A

141090466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857520-T-C

141090677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857357-G-A

141090677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857357-G-T

141090893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857151-A-G

141091031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96857050-G-A

http://identifiers.org/hco/3/GRCh38#141091329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96856824-C-A

141091329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856824-C-G

141091329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856824-C-T

141091336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856817-A-G

141091581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856600-A-G

141091585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856596-G-A

141091783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856424-C-T

141091794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856413-A-G

141091800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856409-C-T

141092121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856150-G-A

141092166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856105-C-T

141092174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856097-A-G

141092223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96856050-G-A

141093860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96855658-G-T

141094336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96855228-C-T

141094781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96854881-C-G

141094962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96854661-T-C

141095196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96854385-G-T

141095594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853951-G-A

141095594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853951-G-T

141095769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853832-C-T

141096760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853299-T-G

141096936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853149-C-T

141096961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853124-T-C

141097012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853072-T-A

141097012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96853072-T-C

141097200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96852913-T-G

141097240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96852882-A-G

141097354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96852768-T-C

141099511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849705-C-T

141099543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849671-G-A

141099624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849585-A-G

141099790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849422-G-A

141099903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849305-T-G

141099941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96849269-G-C

141100342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848969-T-G

141100346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848965-A-T

141100463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848860-G-A

141100504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848825-G-C

http://identifiers.org/hco/3/GRCh38#141100606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96848708-A-C

141100627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848690-C-T

141101143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848248-G-A

141101304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848127-C-T

141101372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848062-G-C

141101431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96848015-G-A

141101462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96847984-C-T

141101728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96847735-G-A

141101788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96847672-C-T

141102119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96846846-G-T

141102144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96846821-A-G

141102657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96846334-A-G

141102671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96846320-G-T

141102843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96846140-A-G

http://identifiers.org/hco/3/GRCh38#141103597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96845426-C-A

141103675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845353-C-T

141103731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845317-G-A

141103869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845196-A-G

141103869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845196-A-T

141103876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845189-C-T

141103949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845119-A-T

141103966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96845102-G-A

141104572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96844533-C-T

141104901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96844214-C-G

http://identifiers.org/hco/3/GRCh38#141104941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96844170-C-A

141105095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96844055-A-G

141105169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843977-G-A

141105219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843928-C-T

141105438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843772-T-C

141105675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843512-A-G

141105888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843320-T-C

141106016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96843180-C-T

http://identifiers.org/hco/3/GRCh38#141106033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96843163-A-C

141106097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843099-G-A

141106097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843099-G-T

141106194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96843006-T-G

141106229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842967-A-T

141106282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842911-T-C

141106393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842782-C-T

141106609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842354-C-T

141106813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842164-C-T

141106817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842160-C-G

141106817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96842160-C-T

141106902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841942-A-G

141107323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841496-T-C

141107591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841293-A-G

141107664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841221-T-C

141107664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841221-T-G

141107862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841099-C-T

141107944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841029-G-C

141107966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96841007-T-A

141108079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840873-C-G

141108115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840837-C-T

141108306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840660-G-A

141108357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840620-G-A

141108613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840386-G-A

141108613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840386-G-T

http://identifiers.org/hco/3/GRCh38#141108614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96840385-A-C

141108717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840295-G-C

http://identifiers.org/hco/3/GRCh38#141108949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96840068-A-C

141108966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840048-C-T

141108987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96840030-G-A

141109558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96839486-A-G

141109734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96839293-T-G

141109735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96839292-C-T

141109843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96839189-T-C

141109867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96839161-T-G

141111543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96838438-G-A

141111866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96838110-C-T

141111867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96838109-G-A

141112008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837947-G-C

141112062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837889-C-T

141112215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837747-T-C

http://identifiers.org/hco/3/GRCh38#141112280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96837685-C-A

141114550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837442-C-G

141114554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837438-A-T

141114640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837358-A-G

141114701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837302-T-C

http://identifiers.org/hco/3/GRCh38#141114980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96837045-C-A

141114980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837045-C-T

141114992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96837033-A-G

http://identifiers.org/hco/3/GRCh38#141115675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96836732-C-A

141115675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96836732-C-T

http://identifiers.org/hco/3/GRCh38#141115761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96836646-C-A

141115917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96836497-C-T

141115983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96836444-C-T

141116088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96836343-C-T

141116140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96836304-A-G

http://identifiers.org/hco/3/GRCh38#141116147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96836297-C-A

141116495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96835942-A-G

http://identifiers.org/hco/3/GRCh38#141116565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96835903-C-A

141116565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96835903-C-T

141116683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96835787-G-A

http://identifiers.org/hco/3/GRCh38#141116938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96835561-C-A

141117093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96835232-A-G

141117211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96835121-T-A

141117211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96835121-T-C

141123251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96834611-C-T

141123480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96834399-C-T

http://identifiers.org/hco/3/GRCh38#141123739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96834164-C-A

141123976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96833883-A-G

http://identifiers.org/hco/3/GRCh38#141123977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96833882-C-A

141124030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96833811-T-C

141124323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96833533-G-A

141124388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96833470-G-A

141124512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96833373-C-T

141125060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832930-G-A

141126893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832315-T-G

141127000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832213-C-G

141127001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832212-C-T

141127032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832194-G-A

141127136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832105-G-A

141127154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832087-G-C

141127165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96832073-T-C

141127448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96831807-C-T

141145347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96828692-A-G

141145733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96828257-A-T

141146996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96826877-A-G

141146996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96826877-A-T

http://identifiers.org/hco/3/GRCh38#141147057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96826823-C-A

141147057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96826823-C-T

141147117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96826779-T-C

141147272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96826625-C-T

141147284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96826614-G-A

141147387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96826573-C-G

141147387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96826573-C-T

http://identifiers.org/hco/3/GRCh38#141147391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96826568-C-A

141147391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96826568-C-T

http://identifiers.org/hco/3/GRCh38#141147619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96826450-A-C

141147619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826450-A-G

141147627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826442-G-T

141147630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826437-T-C

141147653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826414-G-A

141147656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826411-A-G

http://identifiers.org/hco/3/GRCh38#141147676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96826393-C-A

141147676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826393-C-G

141147676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826393-C-T

141147691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826380-A-T

http://identifiers.org/hco/3/GRCh38#141147724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#96826344-C-A

141147724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826344-C-T

141147725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826343-G-A

141147725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826343-G-T

141147738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826330-T-C

141147919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826185-T-C

141147919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 96826185-T-G

141147940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826168-T-A

141147954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826158-A-G

141147998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826109-G-A

141147998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96826109-G-T

141148106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825992-T-C

141148262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825860-C-T

141148268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825854-C-T

http://identifiers.org/hco/3/GRCh38#141148287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96825835-C-A

141148312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825811-A-G

141148313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825810-T-C

141148409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825715-G-A

141148409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825715-G-T

http://identifiers.org/hco/3/GRCh38#141148431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96825689-C-A

141148431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: 96825689-C-G

http://identifiers.org/hco/3/GRCh38#141148507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30630
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#96825616-C-A