70992698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912149-T-C

70992739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912191-G-A

70992741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912193-C-G

70992774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912215-A-G

70992802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912246-A-G

70992986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912399-G-A

http://identifiers.org/hco/4/GRCh38#70992987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912400-C-A

70992987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912400-C-T

http://identifiers.org/hco/4/GRCh38#70993043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912444-C-A

70993053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912454-C-T

70993074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912483-G-A

70993074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88912483-G-T

70993328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912692-C-T

70993331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912695-A-G

70993365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912724-T-C

70993372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912732-G-A

70993372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912732-G-T

http://identifiers.org/hco/4/GRCh38#70993376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912736-A-C

70993376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912736-A-T

70993385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912747-G-A

70993385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912747-G-T

70993392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912754-T-A

70993392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912754-T-C

70993409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912777-T-C

http://identifiers.org/hco/4/GRCh38#70993454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912802-C-A

70993458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912806-T-C

70993468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912816-T-C

70993481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912828-G-A

70993481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912828-G-C

70993542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912877-T-C

70993543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-A

70993543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-C

70993543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912878-G-T

70993556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912891-C-T

70993561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912896-G-T

70993565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912900-G-A

70993565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912900-G-C

http://identifiers.org/hco/4/GRCh38#70993602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88912937-C-A

70993602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88912937-C-T

70993725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 88913045-C-G

http://identifiers.org/hco/4/GRCh38#70993913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913192-C-A

70993913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 88913192-C-T

70993987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88913248-T-A

http://identifiers.org/hco/4/GRCh38#70994001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913250-C-A

70994009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88913258-A-G

http://identifiers.org/hco/4/GRCh38#70994141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88913299-C-A

70994176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88913331-C-T

70994312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88913433-C-G

70994486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88913606-C-T

70994520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88913636-A-T

70994792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914031-T-G

70994929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88914165-A-G

70995090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914311-T-C

70995179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914379-T-C

70995179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914379-T-G

70996560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914884-G-A

70996637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88914955-T-C

70996953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915413-T-C

70997030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915486-T-C

70997227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915653-C-G

70997274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915679-T-C

70997330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915729-A-G

70997388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915784-T-C

70997460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915862-C-T

70997494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88915907-G-A

70997613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88916096-C-T

70997674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88916156-A-G

70997677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88916159-T-C

70997959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88917356-G-T

70997972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88917366-G-T

70997976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88917370-G-T

70998017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88917412-T-C

70998125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88917521-G-C

http://identifiers.org/hco/4/GRCh38#70998188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88917584-A-C

70998188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88917584-A-G

http://identifiers.org/hco/4/GRCh38#71006223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918114-C-A

71006223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918114-C-T

71006246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918142-G-A

71006246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918142-G-T

http://identifiers.org/hco/4/GRCh38#71006256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918152-C-A

71006256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918152-C-T

http://identifiers.org/hco/4/GRCh38#71006265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88918161-C-A

71006265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918161-C-G

71006265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918161-C-T

71006330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918218-G-A

71006342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918230-A-G

71006345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88918233-T-C

71022307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88920427-T-G

http://identifiers.org/hco/4/GRCh38#71022315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88920435-C-A

71022315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88920435-C-T

71022390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88920512-T-A

71022390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88920512-T-C

71022390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88920512-T-G

71022396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88920518-G-A

71022396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88920518-G-C

71022396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88920518-G-T

71022495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88920617-G-A

71022578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88920698-G-A

71022578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88920698-G-T

71022604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88920717-T-A

71022604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88920717-T-G

71022951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921192-T-A

71022976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921217-G-C

71022976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921217-G-T

71023032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921268-C-T

71023128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921508-A-G

71023212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921613-C-T

71023217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921616-A-G

http://identifiers.org/hco/4/GRCh38#71023332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88921726-C-A

71023372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921761-G-T

71023447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921847-G-A

71023447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921847-G-T

71023471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921871-G-T

71023475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921875-A-G

71023533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921915-A-G

71023533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921915-A-T

71023535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921917-G-A

71023535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921917-G-C

71023535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88921917-G-T

http://identifiers.org/hco/4/GRCh38#71023703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88922085-A-C

71023725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88922110-G-T

71023737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88922122-A-G

71023770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88922152-G-T

71023776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88922158-T-G

71023787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88922169-A-G

71024175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88923041-G-A

71024269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88923119-C-T

71024316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88923163-G-T

71025272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924187-C-T

71025456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924361-G-A

71025563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924477-C-T

71025622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924520-C-T

71025666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924566-G-T

71025673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924573-G-A

71025673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924573-G-C

71025713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924629-G-A

71025713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924629-G-T

71025753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924664-T-C

http://identifiers.org/hco/4/GRCh38#71025763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88924674-C-A

71025763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88924674-C-T

71026383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88925986-T-C

71026400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88926006-C-T

71026403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88926009-C-T

http://identifiers.org/hco/4/GRCh38#71026537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88926108-C-A

71026537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88926108-C-T

71026539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88926110-A-G

http://identifiers.org/hco/4/GRCh38#71026580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88926151-C-A

71026627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88926190-A-T

71026737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88926293-T-C

71026803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88926360-T-C

71027128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88926883-C-G

71027219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88926976-A-G

71027261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927010-A-G

71027263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927012-G-A

71027305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927055-T-C

71027410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927156-G-T

71027475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927204-A-G

71027588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927337-C-T

71027674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88927406-G-A

71028212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88928722-C-T

71028301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88928831-A-G

71029269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929009-A-G

71029269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929009-A-T

71029278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929018-T-G

71029311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929050-G-A

71029328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929062-A-G

71029328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88929062-A-T

http://identifiers.org/hco/4/GRCh38#71029395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88929121-A-C

71029395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88929121-A-G

http://identifiers.org/hco/4/GRCh38#71029401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88929127-C-A

71029401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88929127-C-T

71029413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88929139-A-G

71029413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 88929139-A-T

http://identifiers.org/hco/4/GRCh38#71029462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88929192-C-A

71029501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929232-G-T

71029525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929288-T-A

71029525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929288-T-C

71029525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929288-T-G

71029532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929295-A-G

71029532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929295-A-T

http://identifiers.org/hco/4/GRCh38#71029534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88929297-A-C

71029534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929297-A-G

71029534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929297-A-T

71029551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929306-T-A

71029551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929306-T-C

71029557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929312-T-A

71029557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929312-T-C

71029563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929318-T-A

71029563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929318-T-C

http://identifiers.org/hco/4/GRCh38#71029605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88929355-C-A

71029605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929355-C-T

71029612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929362-G-A

71029612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929362-G-T

71029615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929365-A-T

71029618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929368-G-A

71029676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929428-G-T

71029773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929519-A-G

71029787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929533-A-G

71029791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929536-T-A

71029833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929577-A-G

71029857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88929594-T-C

http://identifiers.org/hco/4/GRCh38#71029974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88930476-C-A

71029977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930479-G-A

71029977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930479-G-T

71030031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930532-G-A

71030031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930532-G-C

71030235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930721-C-G

71030295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930785-A-G

71030328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930823-G-T

71030329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930824-C-T

71030383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930878-G-A

71030383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930878-G-T

71030408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930898-A-G

http://identifiers.org/hco/4/GRCh38#71030413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88930903-C-A

71030482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88930976-T-C

http://identifiers.org/hco/4/GRCh38#71030523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88931005-A-C

71030523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88931005-A-G

http://identifiers.org/hco/4/GRCh38#71030526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88931008-C-A

http://identifiers.org/hco/4/GRCh38#71030549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#88931031-C-A

71030619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88931093-T-C