http://identifiers.org/hco/6/GRCh38#107867762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42708503-C-A

107867958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42708301-G-C

http://identifiers.org/hco/6/GRCh38#107868115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42708145-C-A

107868115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42708145-C-G

107868189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42708067-G-A

107868584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707898-G-A

107868585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707897-A-G

107869014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707386-T-C

107869034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707358-G-A

107869034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707358-G-T

107869068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707347-G-T

107869116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707302-T-C

107869207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707222-A-G

107869312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42707137-T-C

107869606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706917-G-T

107869977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706600-G-A

107869977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706600-G-T

107869988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706592-T-C

107870014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706566-T-C

107870053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706548-C-G

107870053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706548-C-T

107870059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706542-G-A

107870059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706542-G-T

http://identifiers.org/hco/6/GRCh38#107870116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42706500-C-A

107870127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706489-A-G

107870197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 42706467-T-C

107870363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706334-G-T

107870626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3 prime UTR variant
orthologous variants: 42706076-G-T

107871001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705713-T-C

107871022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705692-T-C

107871201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705520-T-C

107871386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705325-C-T

http://identifiers.org/hco/6/GRCh38#107871539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42705180-C-A

107871539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705180-C-G

http://identifiers.org/hco/6/GRCh38#107871573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42705152-C-A

107871573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705152-C-T

http://identifiers.org/hco/6/GRCh38#107871606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42705120-C-A

107871613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705113-A-G

107871613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705113-A-T

107871620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705107-T-A

107871640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42705088-A-T

107871866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704869-T-C

107871867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704868-G-A

107871867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704868-G-T

107871877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704858-G-A

107871939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704800-A-T

107871945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704794-A-T

http://identifiers.org/hco/6/GRCh38#107871968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42704773-C-A

http://identifiers.org/hco/6/GRCh38#107871975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42704766-A-C

http://identifiers.org/hco/6/GRCh38#107872037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42704712-A-C

107872066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704681-C-T

107872144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704595-C-G

107872311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704434-C-T

107872364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704383-T-A

107872660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42704069-G-T

107872860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42703923-A-G

107872893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42703890-G-A

107873017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42703797-G-T

107873897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42702546-C-G

107873959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42702500-G-C

107876583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42699954-G-A

107876583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42699954-G-C

107876583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42699954-G-T

http://identifiers.org/hco/6/GRCh38#107876670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42699862-C-A

107876670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42699862-C-T

http://identifiers.org/hco/6/GRCh38#107876674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42699858-A-C

http://identifiers.org/hco/6/GRCh38#107876678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42699854-A-C

107876682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699850-A-G

107876779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699768-T-A

107876779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699768-T-C

http://identifiers.org/hco/6/GRCh38#107876784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42699763-C-A

107876784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699763-C-T

107876785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699762-A-G

107876785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699762-A-T

107876786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42699757-A-T

107877176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42698875-A-T

107877263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42698790-T-C

107880755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692852-A-T

107880782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692825-C-T

107880838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692764-G-A

107880838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692764-G-T

107880900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692705-G-A

107880900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692705-G-T

http://identifiers.org/hco/6/GRCh38#107880903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42692703-C-A

107880903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692703-C-G

107880903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692703-C-T

107880916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42692690-A-G

107881074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692536-G-A

107881074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692536-G-T

http://identifiers.org/hco/6/GRCh38#107881075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42692535-C-A

107881075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692535-C-G

107881101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692511-G-A

http://identifiers.org/hco/6/GRCh38#107881125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42692487-C-A

107881125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692487-C-G

107881125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42692487-C-T

107882541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691666-C-T

107882548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691659-C-T

107882636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691592-A-G

107882707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691529-G-A

107882896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691354-A-G

107882896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691354-A-T

107882953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691305-C-T

107882979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42691225-A-G

107883019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42691176-T-C

107883064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42691131-T-C

107883118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42691077-T-A

107883230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42690965-A-G

107883236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42690959-A-G

107893470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42688844-T-C

107893709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688634-G-T

107893716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688625-G-A

107893716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688625-G-C

107893729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688603-G-A

http://identifiers.org/hco/6/GRCh38#107893773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42688552-A-C

107893775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688550-T-C

107893820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688511-G-A

http://identifiers.org/hco/6/GRCh38#107893822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42688509-A-C

107893822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688509-A-T

107893826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42688505-C-T

107893848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42688479-G-T

107893938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42688400-T-A

107893938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42688400-T-G

http://identifiers.org/hco/6/GRCh38#107893951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42688387-C-A

107894564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42687993-T-C

107898737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42685027-C-T

107898882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42684885-T-G

107899130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42684691-G-A

107899369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42684549-T-C

107900010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683849-G-A

107900030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683829-G-A

107900902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683476-A-T

107900928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683455-A-G

107901098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683317-T-G

107901109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42683258-C-T

107901277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42682875-T-C

107901277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42682875-T-G

http://identifiers.org/hco/6/GRCh38#107901559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42682472-A-C

107901568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42682463-T-G

107901772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42682288-G-A

107902399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42681732-T-C

107902437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42681694-A-G

107902465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42681565-T-C

http://identifiers.org/hco/6/GRCh38#107902828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42681238-A-C

107903040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42681025-T-C

107903065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42681015-T-A

107903347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42680278-T-G

http://identifiers.org/hco/6/GRCh38#107903390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42680242-C-A

http://identifiers.org/hco/6/GRCh38#107904829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42679767-C-A

107904829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42679767-C-T

107904853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42679743-G-A

107904853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42679743-G-T

107904941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42679663-A-T

107905256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42678800-A-G

107905540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42678541-T-C

107905739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42678357-C-G

http://identifiers.org/hco/6/GRCh38#107905752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42678262-A-C

107905752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42678262-A-G

107906732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42677672-T-C

http://identifiers.org/hco/6/GRCh38#107907026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42677428-A-C

http://identifiers.org/hco/6/GRCh38#107907027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42677427-C-A

107907092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42677348-G-C

107907092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42677348-G-T

107907796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676750-A-T

107907888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676663-A-G

107907937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676625-C-T

107907957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676616-A-G

107907984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676589-T-C

107908890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42674883-A-G

107908891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42674882-T-C

107909412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42674692-A-G

http://identifiers.org/hco/6/GRCh38#107909602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42674515-C-A

107909723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42674388-C-T

http://identifiers.org/hco/6/GRCh38#107909881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42674245-A-C

107909932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron variant
orthologous variants: 42674192-T-G

107911501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673589-T-C

107911510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673586-T-C

107911547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673566-G-A

107912003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673149-T-A

107912626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672347-T-C

107912626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672347-T-G

http://identifiers.org/hco/6/GRCh38#107912634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42672339-C-A

107912634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672339-C-G

107912634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672339-C-T

http://identifiers.org/hco/6/GRCh38#107912647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42672325-C-A

107912647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672325-C-T

107912664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672308-A-G

http://identifiers.org/hco/6/GRCh38#107912680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42672294-A-C

107912680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672294-A-G

107912690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672284-A-G

107913033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671958-T-C

http://identifiers.org/hco/6/GRCh38#107913479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42670717-A-C

107921878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42667204-T-G

http://identifiers.org/hco/6/GRCh38#107921971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42667129-A-C

107922207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666905-A-G

107922561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666861-A-G

107924733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665491-A-G

107924765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665459-G-T

107925026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42665198-G-A

107925026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42665198-G-C

107925026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42665198-G-T

107925027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42665197-T-C

107925454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42664789-C-T

107926865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42661247-A-G

107927060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42661065-G-A

107927559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42660910-T-C

107928125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42660315-T-C

107928906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42659950-C-T

107928971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42659900-T-C

107929683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42659274-C-T

107932153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42658347-A-G

http://identifiers.org/hco/6/GRCh38#107932156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42658344-C-A

107932156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42658344-C-G

107932156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42658344-C-T

107932177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42658323-A-G

107932177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42658323-A-T

107932277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42658229-T-C

107944861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646325-T-C

http://identifiers.org/hco/6/GRCh38#107944865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42646320-C-A

107944865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646320-C-T

107948210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42644642-T-C

107951424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42640515-T-C

107952201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42639917-A-G

107952201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42639917-A-T

107956418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42639246-T-G

107956510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42639187-A-G

107956838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42638918-T-C

107956870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42638886-A-G

107956928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42638850-C-T

107957166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42638609-C-T

http://identifiers.org/hco/6/GRCh38#107957507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42638257-C-A

107957625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638140-G-A

107957663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638115-G-A

107957740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638034-A-G

107957740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638034-A-T

107957766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638014-G-A

107957766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42638014-G-T

107957805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42637976-G-A

107957805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42637976-G-T

107957847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42637926-G-A

107957847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42637926-G-T

http://identifiers.org/hco/6/GRCh38#107957866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42637908-C-A

107957866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42637908-C-G

107957866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42637908-C-T

107958042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 42637726-G-A

107958042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 42637726-G-C

107958042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 42637726-G-T

107958051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 42637717-A-G

http://identifiers.org/hco/6/GRCh38#107958113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42637647-C-A

107958113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42637647-C-G

107958113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42637647-C-T

http://identifiers.org/hco/6/GRCh38#107958178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21082
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42637571-C-A