99850170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron variant
orthologous variants: 116601851-C-T

99850434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron variant
orthologous variants: 116601656-G-A

99850434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron variant
orthologous variants: 116601656-G-T

http://identifiers.org/hco/1/GRCh38#99850499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116601591-C-A

99850499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116601591-C-T

99850608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116601488-A-G

99850608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116601488-A-T

99850752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116601325-G-A

http://identifiers.org/hco/1/GRCh38#99850853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116601240-C-A

http://identifiers.org/hco/1/GRCh38#99850906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116601187-C-A

99850906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116601187-C-G

99850906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116601187-C-T

99850997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116601042-G-A

99851022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116601017-T-C

99851126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 116600913-T-C

99851126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 116600913-T-G

99851183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600864-G-T

99851400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600455-T-C

http://identifiers.org/hco/1/GRCh38#99851728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116600044-C-A

99851945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599812-G-A

99851948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599809-T-G

99852055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599701-T-G

99852232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599526-T-G

http://identifiers.org/hco/1/GRCh38#99852276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116599480-A-C

99852767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599320-A-T

99852828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599262-A-G

99852835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599255-C-T

99853234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116598919-C-T

99853251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116598902-A-G

99853325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116598828-C-T

99853400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116598757-T-C

99853537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116598635-T-C

99854434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597795-T-A

99854434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597795-T-G

99855028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597330-C-G

99855028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597330-C-T

99855029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597329-T-A

99855029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597329-T-C

99855196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597132-G-A

99855215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116597113-A-G

99856053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116595573-G-C

99856201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116595462-C-T

http://identifiers.org/hco/1/GRCh38#99856291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116595377-C-A

99856291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116595377-C-T

99860645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116588292-A-T

99860745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116588199-C-T

99860762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116588182-C-T

99860787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116588157-A-G

99860859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116588090-A-G

99861146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587847-C-G

99861146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587847-C-T

99861167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587827-A-G

99861187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587807-T-C

99861187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587807-T-G

99861191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587803-G-A

99861205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116587781-G-A

99861221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587753-T-C

99861236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587740-T-A

http://identifiers.org/hco/1/GRCh38#99861246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116587730-A-C

99861246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587730-A-G

99861276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587701-G-A

99861276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587701-G-C

99861289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587688-G-A

99861303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587674-G-C

99861303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587674-G-T

99861352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587625-A-G

99861474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587511-G-A

99861474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116587511-G-T

99861643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116587329-G-A

99861685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116587287-G-T

99861794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116587208-T-A

99861794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116587208-T-C

99861794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116587208-T-G

99862005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116586902-G-A

99862014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116586893-T-C

99862035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116586872-T-C

99862163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585913-G-A

99862185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585891-G-A

99862185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585891-G-T

http://identifiers.org/hco/1/GRCh38#99862187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116585889-C-A

99862233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585852-T-G

99862303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116585785-C-T

99862484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585605-T-C

99863378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585427-A-T

99864207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116585018-G-A

http://identifiers.org/hco/1/GRCh38#99864264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116584974-C-A

99864264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584974-C-T

99864324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584912-T-C

99864324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584912-T-G

99864362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584878-G-A

99864362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584878-G-T

99864451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116584791-G-A

99864511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116584731-G-A

99864551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116584691-A-G

99864565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116584677-A-G

99864720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116584445-T-G

99865592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583833-G-T

99865642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583795-G-A

http://identifiers.org/hco/1/GRCh38#99865931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116583537-A-C

99866032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583354-C-T

99866040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583346-G-T

99866076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583319-T-G

99866161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583291-G-C

http://identifiers.org/hco/1/GRCh38#99866332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116583156-C-A

99866361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583129-A-G

99866396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116583090-A-G

http://identifiers.org/hco/1/GRCh38#99866431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116583061-C-A

99866529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116582973-T-C

99870492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116582262-G-A

99870492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116582262-G-C

99870492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116582262-G-T

99870578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116582176-G-A

99870631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116582133-G-A

99870631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116582133-G-T

99870645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116582119-T-C

http://identifiers.org/hco/1/GRCh38#99870697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116582071-C-A

http://identifiers.org/hco/1/GRCh38#99870763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116582024-C-A

99870873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581914-A-G

99870883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581904-A-T

99870888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581899-A-G

99870888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581899-A-T

99870970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581812-G-A

99870972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581810-A-G

99870981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581801-G-A

99870981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581801-G-T

99871943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581617-T-C

99872002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581549-T-C

99872216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581266-T-C

99872245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116581236-G-A

99874674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116581013-T-C

99874674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116581013-T-G

99874765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116580922-G-A

99874781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116580906-C-T

99874935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580673-T-A

99875049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580562-C-T

http://identifiers.org/hco/1/GRCh38#99875115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116580501-C-A

99875115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580501-C-T

99875278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580345-C-G

http://identifiers.org/hco/1/GRCh38#99875442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116580190-C-A

99875569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580064-A-G

99875586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580047-G-T

http://identifiers.org/hco/1/GRCh38#99875604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116580029-A-C

99875604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116580029-A-G

http://identifiers.org/hco/1/GRCh38#99876314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116578984-A-C

99876314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578984-A-G

99876314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578984-A-T

http://identifiers.org/hco/1/GRCh38#99876364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116578931-C-A

99876364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578931-C-G

99876364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578931-C-T

http://identifiers.org/hco/1/GRCh38#99876494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116578810-C-A

99876494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116578810-C-T

99876498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578806-G-C

99876534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578770-T-C

99876573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578731-C-T

99876643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578661-T-C

99876645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578659-G-A

99876645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578659-G-T

http://identifiers.org/hco/1/GRCh38#99877526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116578397-C-A

99877526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578397-C-T

99877597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578329-A-G

99877601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578325-T-C

http://identifiers.org/hco/1/GRCh38#99877611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116578315-A-C

99877751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578177-T-A

99877751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578177-T-C

99877754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116578174-A-T

99877954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116578006-A-G

99878019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116577956-G-A

99878385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116577663-T-A

99878385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116577663-T-C

99879198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116576696-A-G

99880395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575606-A-T

99880416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575585-T-C

99880468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575537-T-G

99880532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575479-G-C

99880532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575479-G-T

99880533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575478-A-G

99880533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575478-A-T

99880534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575477-T-A

99880536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575475-T-A

99880536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575475-T-G

99880570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575448-A-G

http://identifiers.org/hco/1/GRCh38#99880602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116575428-A-C

99880613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575417-A-G

99880745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116575285-G-A

99880772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116575258-C-T

99880881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575154-A-G

http://identifiers.org/hco/1/GRCh38#99881030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116575029-C-A

99881061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575000-G-A

99881061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116575000-G-T

99881110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574957-C-T

99881112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574955-A-G

99881112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574955-A-T

http://identifiers.org/hco/1/GRCh38#99881267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116574820-C-A

http://identifiers.org/hco/1/GRCh38#99881271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116574815-C-A

99881340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574746-G-A

99881358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574728-G-A

99881358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574728-G-T

http://identifiers.org/hco/1/GRCh38#99881376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116574710-A-C

99881445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 116574641-C-T

99881468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116574614-T-G

http://identifiers.org/hco/1/GRCh38#99881526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116574538-C-A

99881556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574508-G-A

99881556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116574508-G-C

99882263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116574177-T-G

99882306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116574126-A-G

99882306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116574126-A-T

99882521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116573955-C-T

http://identifiers.org/hco/1/GRCh38#99882567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116573894-C-A

http://identifiers.org/hco/1/GRCh38#99884087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116573058-A-C

99884087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116573058-A-G

99884102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116573043-G-A

99884158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116572989-G-A

99884218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116572929-A-G

99884258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572889-T-C

99884260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572887-A-G

99884333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116572820-T-C

99884370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116572783-G-A

99884370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116572783-G-C

99884491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572661-T-G

99884502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572461-T-C

http://identifiers.org/hco/1/GRCh38#99884669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116572300-A-C

99884805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572162-A-G

http://identifiers.org/hco/1/GRCh38#99884814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116572153-C-A

99884833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572134-G-A

99884833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116572134-G-T

99887872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116570402-A-G

http://identifiers.org/hco/1/GRCh38#99887878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116570396-C-A

http://identifiers.org/hco/1/GRCh38#99888190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116570159-C-A

http://identifiers.org/hco/1/GRCh38#99888214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116570149-C-A

99888214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116570149-C-T

99889985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567876-A-G

99890114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567758-G-A

99890159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567715-G-T

99890312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567574-A-T

99890436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567395-G-A

http://identifiers.org/hco/1/GRCh38#99890490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116567275-C-A

99890490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567275-C-T

99890547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116567225-G-A

99890749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566981-T-C

99890929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566823-A-G

99890993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566759-A-G

99891078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566670-G-A

99891078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566670-G-T

http://identifiers.org/hco/1/GRCh38#99891110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116566639-C-A

99891110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566639-C-T

99891184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566577-C-G

99891201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566564-C-T

http://identifiers.org/hco/1/GRCh38#99891202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116566563-A-C

99891202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566563-A-G

99891264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116566503-G-A

99891264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116566503-G-T

99891291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116566476-T-A

99891380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566387-C-G

http://identifiers.org/hco/1/GRCh38#99891386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116566381-A-C

99891386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566381-A-T

http://identifiers.org/hco/1/GRCh38#99891466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116566309-C-A

99891466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566309-C-T

99891727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116566046-A-G

99891782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116566009-A-G

99891867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116565920-G-A

99891867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116565920-G-C

99892284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116565331-A-G

http://identifiers.org/hco/1/GRCh38#99892332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116565240-A-C

99892332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116565240-A-G

99892632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116564957-A-G

99894313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116563548-G-A

99894313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116563548-G-C

99895633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116562846-A-G

http://identifiers.org/hco/1/GRCh38#99896182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116562590-C-A

99896182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116562590-C-T

99896357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116562464-C-T

99896411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116562333-G-T

99896561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561950-G-A

99896603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561915-T-C

99896690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561842-G-A

99896690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561842-G-C

99896772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561767-T-G

99896810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561730-T-G

99896856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561687-G-A

99896864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116561679-G-T

http://identifiers.org/hco/1/GRCh38#99897278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116561278-A-C

99900573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552623-T-G

99900691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116552508-C-T

99900703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116552496-A-G

99900771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116552428-A-G

99900836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116552363-C-G

99900964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552260-T-C

99902551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552125-G-A

99902592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552084-A-G

99902592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552084-A-T

99902713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116551967-G-A

99902892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116551804-G-A

99902892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116551804-G-T

99902920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116551779-T-G

http://identifiers.org/hco/1/GRCh38#99902931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116551768-A-C

99902931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116551768-A-G

http://identifiers.org/hco/1/GRCh38#99902968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116551732-A-C

99902968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116551732-A-G

99910467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548916-G-A

99910592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548810-G-A

99910859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548508-G-A

99910859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548508-G-C

99910861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548506-T-C

99910867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548500-G-A

99910867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548500-G-T

99910873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548481-T-A

99910930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548430-A-G

http://identifiers.org/hco/1/GRCh38#99910963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116548392-C-A

99910965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548390-T-C

http://identifiers.org/hco/1/GRCh38#99910994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116548350-C-A

99912364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116547046-G-T

http://identifiers.org/hco/1/GRCh38#99912433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116546982-C-A

99912491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116546924-A-G

99912492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116546923-T-C

99912507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116546908-A-G

99912514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116546901-C-T

99912525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116546890-G-T

99912540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546879-A-G

http://identifiers.org/hco/1/GRCh38#99912584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116546848-C-A

99912584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546848-C-T

99912604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546828-T-C

http://identifiers.org/hco/1/GRCh38#99912617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116546815-C-A

99912617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546815-C-T

99913270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546070-T-C

99913288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116546047-A-G

http://identifiers.org/hco/1/GRCh38#99913827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116545542-C-A

99913856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116545518-A-T

99914310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116545233-T-C

99914592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544955-G-A

99914685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544852-G-A

99914786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544766-G-A

http://identifiers.org/hco/1/GRCh38#99915244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116544255-A-C

99915244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544255-A-T

http://identifiers.org/hco/1/GRCh38#99915265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116544238-C-A

http://identifiers.org/hco/1/GRCh38#99915287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116544216-A-C

99915322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544211-T-C

99915359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544174-A-T

99915510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544021-G-A

99915517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116544014-A-T

99916049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540926-T-C

99916219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540524-A-G

99916275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540487-A-T

http://identifiers.org/hco/1/GRCh38#99916290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116540468-A-C

99916290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540468-A-G

99916290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540468-A-T

99916291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540467-T-A

99916291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540467-T-C

99916291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540467-T-G

99916310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540448-A-T

http://identifiers.org/hco/1/GRCh38#99916340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116540418-A-C

99916392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540369-A-G

99916658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116540100-G-A

99916666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116540092-G-C

99916757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116540016-C-T

http://identifiers.org/hco/1/GRCh38#99916801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116539972-C-A

99916801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539972-C-T

99916833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539940-G-C

99916833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539940-G-T

99916870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539905-A-T

99916871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539904-T-C

99916871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539904-T-G

99917111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539685-A-G

99917213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539583-G-A

99917213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116539583-G-T

99921389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116538719-A-G

99921389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116538719-A-T

99921422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116538691-A-G

99921559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116538557-C-G

99921628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116538488-C-T

99921904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116537975-A-G

99923652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116537071-A-T

http://identifiers.org/hco/1/GRCh38#99923760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116536948-A-C

http://identifiers.org/hco/1/GRCh38#99923782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116536926-C-A

99923856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116536848-A-G

http://identifiers.org/hco/1/GRCh38#99923934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#116536774-C-A

99923934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 321
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116536774-C-T