172325008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379322-T-A

http://identifiers.org/hco/5/GRCh38#172325012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32379318-A-C

172325012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379318-A-G

172325019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379311-T-A

172325019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379311-T-C

172325019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379311-T-G

172325040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379290-T-A

172325040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379290-T-C

172325040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379290-T-G

172325145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379202-A-G

http://identifiers.org/hco/5/GRCh38#172325203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32379151-C-A

172325203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379151-C-T

172325221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379139-A-G

172325221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3 prime UTR variant
orthologous variants: 32379139-A-T

http://identifiers.org/hco/5/GRCh38#172325291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32379068-A-C

172325406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32378962-A-T

http://identifiers.org/hco/5/GRCh38#172333448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32378096-C-A

172333448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32378096-C-T

172333459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32378085-A-G

172333459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32378085-A-T

172333578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32377983-T-C

172333630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32377932-A-G

http://identifiers.org/hco/5/GRCh38#172333885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377684-C-A

172333885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377684-C-G

172333885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377684-C-T

172333937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377646-T-A

http://identifiers.org/hco/5/GRCh38#172334019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377570-C-A

172334037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377552-G-A

172334113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377481-T-G

172334143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32377447-G-T

http://identifiers.org/hco/5/GRCh38#172334214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377379-A-C

http://identifiers.org/hco/5/GRCh38#172334247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377346-C-A

172334247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32377346-C-T

172334265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32377342-A-G

172334278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32377329-T-C

172334402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32377206-G-T

http://identifiers.org/hco/5/GRCh38#172334469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377135-C-A

http://identifiers.org/hco/5/GRCh38#172334563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377070-C-A

http://identifiers.org/hco/5/GRCh38#172334593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32377041-A-C

172334635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376997-A-G

172334740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376838-G-T

172334793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376804-C-T

172334802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376799-G-A

172334836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376765-G-A

172334836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376765-G-T

http://identifiers.org/hco/5/GRCh38#172334843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376758-C-A

172334843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376758-C-T

172334926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376673-G-A

172334951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376617-T-C

172334978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376591-A-G

http://identifiers.org/hco/5/GRCh38#172335002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376575-C-A

172335004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376573-T-C

172335032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376551-T-A

http://identifiers.org/hco/5/GRCh38#172335048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376535-C-A

172335051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376532-G-A

172335051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376532-G-C

172335051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376532-G-T

172335108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376473-G-T

http://identifiers.org/hco/5/GRCh38#172335111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376470-C-A

172335111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376470-C-T

172335281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376348-G-A

172335281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376348-G-C

172335316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376319-G-A

172335316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376319-G-T

http://identifiers.org/hco/5/GRCh38#172335434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376268-C-A

172335434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376268-C-G

172335434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376268-C-T

172335642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376081-T-C

172335655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376068-G-A

172335655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376068-G-C

172335690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376036-G-A

172335690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32376036-G-T

http://identifiers.org/hco/5/GRCh38#172335691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32376035-C-A

172335774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375954-G-A

172335774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375954-G-C

172335774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375954-G-T

http://identifiers.org/hco/5/GRCh38#172335780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375948-C-A

172335791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375930-G-T

172335811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375909-G-A

172335811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375909-G-T

172335839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375881-A-G

172335869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375851-G-A

http://identifiers.org/hco/5/GRCh38#172336114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375647-A-C

172336134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375627-T-C

http://identifiers.org/hco/5/GRCh38#172336202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375557-A-C

172336265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375508-C-G

172336281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375487-A-T

172336301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375462-G-T

http://identifiers.org/hco/5/GRCh38#172336361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375383-C-A

172336361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375383-C-T

http://identifiers.org/hco/5/GRCh38#172336362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375382-C-A

172336362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375382-C-G

172336362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375382-C-T

http://identifiers.org/hco/5/GRCh38#172336380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375364-C-A

172336380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375364-C-T

http://identifiers.org/hco/5/GRCh38#172336381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32375363-C-A

172336381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375363-C-T

172336536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375214-G-A

172336536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375214-G-C

172336536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375214-G-T

172336538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375212-G-A

172336538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375212-G-T

172336542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375208-G-C

172336542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375208-G-T

172336714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375075-G-A

172336714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375075-G-T

172336715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375074-C-G

172336715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32375074-C-T

172336830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374910-A-G

172336849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374891-T-G

http://identifiers.org/hco/5/GRCh38#172336895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374836-C-A

172336895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374836-C-G

http://identifiers.org/hco/5/GRCh38#172336896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374835-A-C

http://identifiers.org/hco/5/GRCh38#172336925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374819-A-C

172336930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374814-T-C

172336952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374784-G-C

172336966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374776-T-C

http://identifiers.org/hco/5/GRCh38#172336979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374763-C-A

172336979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374763-C-T

http://identifiers.org/hco/5/GRCh38#172337006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374742-C-A

http://identifiers.org/hco/5/GRCh38#172337121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374645-C-A

172337152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374613-G-A

172337152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374613-G-C

172337259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374557-A-G

172337259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374557-A-T

http://identifiers.org/hco/5/GRCh38#172337261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374555-C-A

172337261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374555-C-T

http://identifiers.org/hco/5/GRCh38#172337296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374511-C-A

172337296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374511-C-T

172337440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374353-T-C

172337452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374339-A-G

http://identifiers.org/hco/5/GRCh38#172337490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32374303-C-A

172337494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374299-A-G

172337537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374262-T-C

172337642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374168-G-A

172337857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374025-T-C

172337857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32374025-T-G

172337942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373937-G-A

172337962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373919-G-A

172338044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373844-G-T

http://identifiers.org/hco/5/GRCh38#172338045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373843-A-C

172338045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373843-A-G

172338106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373784-C-T

172338107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373783-T-C

http://identifiers.org/hco/5/GRCh38#172338124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373765-A-C

172338124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373765-A-T

http://identifiers.org/hco/5/GRCh38#172338131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373755-C-A

172338168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373717-T-A

172338168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373717-T-C

http://identifiers.org/hco/5/GRCh38#172338270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373654-C-A

172338270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32373654-C-G

172338649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32373285-C-T

http://identifiers.org/hco/5/GRCh38#172338757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373183-C-A

172338757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32373183-C-T

http://identifiers.org/hco/5/GRCh38#172338794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373137-A-C

http://identifiers.org/hco/5/GRCh38#172338826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32373105-C-A

172338826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32373105-C-T

172339120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372808-T-C

172339219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372709-G-A

172339492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372445-T-G

172339627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372310-T-C

172339713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32372224-C-T

172339747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372190-G-A

172339780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372157-T-C

172339798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372139-A-G

172339822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372115-G-A

172339822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, missense_variant
orthologous variants: 32372115-G-C

172345602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32368791-G-A

172345933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367393-A-G

172345978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367350-C-T

172345985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367343-T-C

172346011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367295-T-A

172346011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367295-T-C

172346384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367011-G-T

172346387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32367008-T-G

172346476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32366926-C-T

172346587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32366817-G-A

172346663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32366764-T-C

172346677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32366747-T-A

http://identifiers.org/hco/5/GRCh38#172347263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32365990-A-C

172347382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365861-T-C

172347407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365836-T-C

172347471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365797-G-A

172347471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365797-G-T

172347527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365754-G-A

172349157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32365009-A-G

172349322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364918-T-C

172350202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364559-T-C

172350203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364558-G-A

172350212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364550-T-C

172350212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364550-T-G

http://identifiers.org/hco/5/GRCh38#172350213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32364549-A-C

http://identifiers.org/hco/5/GRCh38#172350263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32364499-C-A

172350263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364499-C-G

172350263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32364499-C-T

http://identifiers.org/hco/5/GRCh38#172350309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32364468-A-C

172350380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32364408-T-A

172350380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32364408-T-C

172350529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: synonymous variant
orthologous variants: 32364259-G-A

172350529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: synonymous variant
orthologous variants: 32364259-G-C

172350529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: synonymous variant
orthologous variants: 32364259-G-T

172351770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32362321-T-A

172351976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32362109-G-A

172353740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361683-G-A

http://identifiers.org/hco/5/GRCh38#172353775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32361655-C-A

172353775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361655-C-T

http://identifiers.org/hco/5/GRCh38#172353779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32361651-C-A

172353851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361600-A-G

172354137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361338-G-A

172354137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361338-G-T

http://identifiers.org/hco/5/GRCh38#172354140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32361335-C-A

http://identifiers.org/hco/5/GRCh38#172354144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32361331-C-A

172354473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32361065-G-A

172354717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32360830-C-T

172354905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32360684-T-A

172355140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32360488-G-C

172355141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32360487-G-C

172355337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32360322-G-A

172356421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359337-G-A

172356502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359257-G-A

http://identifiers.org/hco/5/GRCh38#172356560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32359209-C-A

172356560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359209-C-G

172356560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359209-C-T

172356580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359189-A-G

172356618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359121-G-A

172356618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32359121-G-T

http://identifiers.org/hco/5/GRCh38#172357475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32358709-C-A

172357608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358617-C-T

172357663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358564-C-G

172357773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358465-C-G

172358105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358232-C-T

172358222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358128-C-T

172358293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32358052-G-A

172358369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357999-C-T

172358476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357899-A-T

http://identifiers.org/hco/5/GRCh38#172358496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32357882-C-A

172358498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357880-G-A

172358634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357744-G-A

172358634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357744-G-C

172358634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357744-G-T

172358639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357739-T-C

http://identifiers.org/hco/5/GRCh38#172358651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32357727-C-A

172358702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357691-A-G

172358964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32357185-C-T

http://identifiers.org/hco/5/GRCh38#172361783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32354846-A-C

172361783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354846-A-G

http://identifiers.org/hco/5/GRCh38#172361826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#32354797-C-A

172361920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32354653-T-C

http://identifiers.org/hco/5/GRCh38#172362001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32354568-C-A

172362080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354505-T-G

172362242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354381-A-G

172362275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354349-A-G

172362355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354247-G-A

172362625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32354039-G-A

172362932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353819-A-G

172362990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353796-T-A

172362990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353796-T-C

172363189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353611-T-A

172363424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353471-G-A

172363726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353203-A-G

172363964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32353008-G-C

172365555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32352269-C-T

172370567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32350192-T-G

172370871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32349742-G-A

172371231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32349244-G-A

172371369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32349128-A-G

172371620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32348886-G-T

172371635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32348871-C-G

172371685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32348820-G-C

172371836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32348675-C-T

172372839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347868-T-A

172372839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347868-T-C

172372882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347827-C-T

172373064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347725-T-G

172373069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347720-T-A

172373154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347650-T-A

172373356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347474-A-T

172373554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347266-G-C

http://identifiers.org/hco/5/GRCh38#172373735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32347128-C-A

172373735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32347128-C-T

http://identifiers.org/hco/5/GRCh38#172373893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32346992-A-C

172373893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346992-A-G

172373893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346992-A-T

http://identifiers.org/hco/5/GRCh38#172373915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32346972-A-C

172373915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346972-A-T

172373931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346956-A-G

http://identifiers.org/hco/5/GRCh38#172373988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32346902-C-A

172373999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346891-C-T

172381867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346710-G-A

172381867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346710-G-C

172381958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346621-G-A

172381958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346621-G-T

172381967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346612-G-T

172381969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346606-G-T

172381987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346582-G-A

172382016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346551-A-G

172382060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32346507-G-A

172382120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32346447-A-G

http://identifiers.org/hco/5/GRCh38#172382596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32346170-C-A

172382596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32346170-C-T

172387341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32343596-G-T

172387868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32343102-G-A

172387917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32343067-T-C

172387928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32343056-A-T

172388005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32342980-C-T

172388599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32342548-C-T

172388688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32342460-G-T

172388775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32342391-C-T

172388839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32342319-C-T

http://identifiers.org/hco/5/GRCh38#172389752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32341652-C-A

172394493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32338066-G-T

172394660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337905-G-C

172394660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337905-G-T

http://identifiers.org/hco/5/GRCh38#172394690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32337885-C-A

172394691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337884-T-G

172394733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337852-G-T

172394738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337847-G-T

172394745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337840-G-A

172394745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337840-G-T

http://identifiers.org/hco/5/GRCh38#172394766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32337819-C-A

172394766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337819-C-G

172394766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32337819-C-T

http://identifiers.org/hco/5/GRCh38#172403355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32334001-C-A

172403423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333949-C-T

172403454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32333919-G-C

172403559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333833-G-A

http://identifiers.org/hco/5/GRCh38#172403631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#32333761-C-A

172403631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32333761-C-G

172403631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32333761-C-T

172403725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333672-C-T

172403742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333658-A-G

172404003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333393-G-A

172404178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32333188-C-T

172406253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331531-T-C

172406264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331520-C-T

172406435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331367-A-G

http://identifiers.org/hco/5/GRCh38#172406486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32331319-C-A

172406486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331319-C-T

http://identifiers.org/hco/5/GRCh38#172406495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32331310-A-C

172406498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331307-G-C

172406498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331307-G-T

172406503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331302-G-A

172406503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331302-G-C

172406503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331302-G-T

172406562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32331244-G-C

172407991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32329632-G-C

http://identifiers.org/hco/5/GRCh38#172408110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32329514-C-A

172408110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32329514-C-T

172408150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32329474-T-A

172408150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32329474-T-C

172408150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32329474-T-G

172415568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32327421-T-C

172415821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32327184-G-A

http://identifiers.org/hco/5/GRCh38#172415868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32327159-C-A

172415868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32327159-C-T

172415919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32327097-C-G

172417026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32326970-C-T

172418317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325644-C-T

http://identifiers.org/hco/5/GRCh38#172418319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32325642-C-A

http://identifiers.org/hco/5/GRCh38#172418330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32325631-C-A

172418445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325529-A-T

172418515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325459-T-A

172418586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325399-C-T

172418732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325242-G-A

172418744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325229-C-T

172418860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32325095-G-A

172418987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324993-G-A

172419753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324335-G-A

172419753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324335-G-T

172419758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324330-A-G

172419758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324330-A-T

172419795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32324292-G-A

172420805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32323071-G-A

http://identifiers.org/hco/5/GRCh38#172420860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32323017-A-C

172420860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32323017-A-G

http://identifiers.org/hco/5/GRCh38#172420903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32322980-A-C

172420903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322980-A-G

172420917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322966-G-A

http://identifiers.org/hco/5/GRCh38#172420948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32322935-C-A

172420979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322904-G-A

http://identifiers.org/hco/5/GRCh38#172421239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32322714-C-A

172421239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322714-C-T

172421366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322593-A-T

172421389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322507-G-A

172421431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32322217-A-G

http://identifiers.org/hco/5/GRCh38#172421677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32321960-C-A

172421749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32321892-G-A

172422149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32321716-C-T

172422321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32321666-A-G

172422462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32321550-G-T

172422483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32321529-C-T

172422505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32321506-G-T

172426157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32319522-A-T

http://identifiers.org/hco/5/GRCh38#172426462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32319245-C-A

172426464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32319243-C-T

172433555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317902-T-C

172433558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317899-G-A

172433602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317878-G-A

172433619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317861-G-A

172433659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317817-T-C

172434302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317431-G-A

172434356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317366-C-G

172434500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317238-G-A

http://identifiers.org/hco/5/GRCh38#172434535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32317214-C-A

172434729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32317058-C-T

172435092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32316959-T-G

172435889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32316513-A-G

172436145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32316295-G-A

172436162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32316279-G-A

172436208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32316243-A-G

172436649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32315819-C-T

172436689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32315792-A-G

172436760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32315736-G-A

172436974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32314973-T-C

172437083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32314886-A-G

172437196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32314737-C-T

172437739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32313751-G-C

172437745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32313745-T-C

172438026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313514-A-G

172438059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313487-G-A

172438254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313354-G-A

172438265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313350-G-C

172438418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313207-T-G

172438568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32313069-C-T

172438738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32312934-C-T

172438741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32312931-A-G

172439946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32311977-C-T

172443195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32308193-T-C

172443589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32307936-C-T

172444591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32307100-G-C

172444795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32306967-C-T

172445148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32306684-C-G

172445230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32306616-C-T

http://identifiers.org/hco/5/GRCh38#172445582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32306482-A-C

172445803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32306294-A-T

172446689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32305341-G-A

172446772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32305261-A-T

172446836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32305201-T-C

172447577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32304480-C-G

172447720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32304359-G-A

172449072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32302872-T-C

172449250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32302730-A-G

172449400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32302597-G-A

172449654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32302351-T-C

172449814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32302162-G-A

172450189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32301816-G-A

172450197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32301808-T-C

172451970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32299838-A-G

172452066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32299766-G-C

172452108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32299751-T-C

172452227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32299626-C-T

172452634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron_variant, undefined
orthologous variants: 32299336-G-A

172452660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32299310-G-A

172452862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32299128-G-A

172453756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32298326-T-A

172453824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32298291-T-C

172454215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32298003-G-A

172454215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: intron variant
orthologous variants: 32298003-G-T

http://identifiers.org/hco/5/GRCh38#172454297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#32297947-C-A

172454297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: missense variant
orthologous variants: 32297947-C-T

172454482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32297823-G-A

172454482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29242
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32297823-G-C