http://identifiers.org/hco/8/GRCh38#125024307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59203887-A-C

http://identifiers.org/hco/8/GRCh38#125024313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59203893-C-A

http://identifiers.org/hco/8/GRCh38#125024326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59203906-A-C

http://identifiers.org/hco/8/GRCh38#125024472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59204026-C-A

125024472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59204026-C-G

125024472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59204026-C-T

125024547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59204097-T-G

125024770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59204311-A-G

125024792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59204334-T-G

125025206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59204602-G-A

125028600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205447-C-G

125028600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205447-C-T

125028734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205577-T-C

125028795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205601-A-G

125028813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205622-A-G

125028897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59205702-G-A

http://identifiers.org/hco/8/GRCh38#125031612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59206355-A-C

125031677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59206417-C-G

125031964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206682-G-A

125031992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206713-T-A

125032029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206744-T-C

http://identifiers.org/hco/8/GRCh38#125032053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#59206768-A-C

125032068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206782-G-A

http://identifiers.org/hco/8/GRCh38#125032075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#59206788-C-A

125032141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206837-T-C

125032186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206883-T-C

125032186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206883-T-G

125032229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59206925-G-C

125032300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 59206996-G-A

125032300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 59206996-G-C

125032300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 59206996-G-T

125032509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59207188-A-G

http://identifiers.org/hco/8/GRCh38#125032570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59207249-C-A

http://identifiers.org/hco/8/GRCh38#125032663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59207314-A-C

125032663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59207314-A-G

125032700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59207347-T-A

125032807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59207466-G-A

125032807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59207466-G-T

125032808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59207467-G-C

125032808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59207467-G-T

125032866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59207523-G-C

125036112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59208636-A-T

125036147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, missense_variant
orthologous variants: 59208669-T-C

125036190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, missense_variant
orthologous variants: 59208711-T-A

125036195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, missense_variant
orthologous variants: 59208716-C-G

125036301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59208818-A-G

125037153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59208961-A-T

125037178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59208984-A-G

125037178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59208984-A-T

http://identifiers.org/hco/8/GRCh38#125037273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59209078-C-A

125037273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: 59209078-C-T

125037328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59209133-G-A

125037328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: stop gained
orthologous variants: 59209133-G-T

125037375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59209174-T-C

125037405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59209202-T-A

125037466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59209239-T-C

125037769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59209707-T-A

125038015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59209960-T-C

125038278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59210339-T-G

125038589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59210556-C-T

125038947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59210880-T-C

125038982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59210914-G-C

125038991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59210923-T-A

125038991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59210923-T-C

125039310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211413-T-C

125039385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211468-T-A

125039386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211469-G-C

125039769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211638-T-C

125039785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211653-T-C

125039924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211791-G-A

125039924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211791-G-C

125039924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211791-G-T

125039954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211817-G-A

125039954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59211817-G-T

125043333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59212118-G-A

125043433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59212223-G-A

http://identifiers.org/hco/8/GRCh38#125043723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59212481-C-A

125043723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59212481-C-T

http://identifiers.org/hco/8/GRCh38#125043817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59212733-C-A

125043817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59212733-C-T

125043837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59212753-C-T

http://identifiers.org/hco/8/GRCh38#125044124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59213040-C-A

125044159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213066-T-A

125044159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213066-T-G

125044185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213091-G-T

125044297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213185-A-G

125044413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213302-T-G

125044440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59213328-G-A

125044517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59213390-T-C

125044542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59213794-C-G

125044542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59213794-C-T

125044658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59213910-T-C

125044779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59214019-G-A

125044779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59214019-G-T

http://identifiers.org/hco/8/GRCh38#125044781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59214021-C-A

125044809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59214135-G-T

125044892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59214219-T-C

125044972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59214283-T-C

http://identifiers.org/hco/8/GRCh38#125044977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59214288-C-A

125045078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214389-C-G

125045078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214389-C-T

125045241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214517-C-T

125045277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214558-T-A

125045308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214579-C-T

125045340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214591-T-C

125045505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59214761-G-T

125046059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59215217-A-G

125046165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59215295-T-A

125046315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59215437-C-T

125046443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59215534-C-T

125047187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59215854-T-C

125047275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59215942-G-A

125047350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216017-A-G

125047423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216084-T-A

125047423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216084-T-C

125048423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216610-T-A

125048423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216610-T-C

125048494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216662-C-G

125048828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59216972-C-T

http://identifiers.org/hco/8/GRCh38#125048866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59217009-C-A

125048866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59217009-C-T

125049926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59217499-C-T

http://identifiers.org/hco/8/GRCh38#125050179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59217753-C-A

125050430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59217957-G-T

http://identifiers.org/hco/8/GRCh38#125050522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59218031-C-A

125050522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218031-C-T

http://identifiers.org/hco/8/GRCh38#125050597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59218096-C-A

125050597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59218096-C-G

125050597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59218096-C-T

125050612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59218111-G-A

125050691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218190-T-C

http://identifiers.org/hco/8/GRCh38#125050760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59218237-C-A

125050768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218245-T-A

125050768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218245-T-C

125055600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59218678-G-A

125055600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59218678-G-T

125055681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218759-A-G

125055688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218771-G-T

125055720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218841-G-C

125055720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218841-G-T

125055742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218863-A-G

125055766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218883-T-C

125055766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218883-T-G

125055772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218889-C-T

125055789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218906-A-G

125055798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218915-C-G

125055800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218917-G-A

125055800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59218917-G-C

125056539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220101-G-A

125056539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220101-G-T

125056555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220116-G-T

125056581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220141-G-C

125056581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220141-G-T

125056618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220179-G-T

125056628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220189-G-T

125056965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59220564-T-C

125057466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221096-G-A

125057466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221096-G-T

125057610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59221196-G-A

125057690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221275-T-A

125057690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221275-T-C

125057765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221347-T-A

125057785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221392-T-A

125057785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221392-T-C

125057813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221417-A-T

125057931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59221536-A-G

125059328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222090-G-A

http://identifiers.org/hco/8/GRCh38#125059413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59222173-C-A

125059413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: 59222173-C-T

http://identifiers.org/hco/8/GRCh38#125059560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59222320-A-C

125059569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222329-A-T

125059598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222344-A-G

125060625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222659-C-T

125060827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222854-T-G

125060877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222900-G-A

125060940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222964-G-A

125060940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59222964-G-T

125061027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223033-G-A

125061027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223033-G-T

125061035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223041-G-A

125061035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223041-G-T

125061229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223469-T-A

125061229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223469-T-C

http://identifiers.org/hco/8/GRCh38#125061302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59223531-C-A

125061302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223531-C-T

125061343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223578-C-G

http://identifiers.org/hco/8/GRCh38#125061368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59223603-A-C

125061461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223688-G-T

125061474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223701-G-A

http://identifiers.org/hco/8/GRCh38#125061526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59223758-C-A

125061526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223758-C-T

125061534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59223766-A-G

125063724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59224550-G-A

125063879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59224777-T-G

125064024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225004-G-A

125064024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225004-G-C

125064048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225028-G-A

125064624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225218-A-G

125064624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225218-A-T

125064801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225380-T-C

125064858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225433-G-A

125064905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225450-T-C

125064930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225468-T-C

125064996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225534-T-C

125065149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59225663-T-C

125065478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59226027-T-C

125067477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227572-T-G

125067555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227649-G-T

125067560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227654-G-T

125067603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: 59227694-T-A

125067616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59227707-T-G

125067735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227827-G-A

125067735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227827-G-T

125067862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227954-T-C

125067865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227957-T-A

125067865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59227957-T-C

125067918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228006-A-G

125067943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228031-T-C

http://identifiers.org/hco/8/GRCh38#125067951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59228039-C-A

http://identifiers.org/hco/8/GRCh38#125068148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59228238-A-C

125068148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228238-A-T

125068289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228610-G-T

125068302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228703-G-T

125068320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228761-C-T

125068361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228802-G-C

125068582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59228976-G-A

http://identifiers.org/hco/8/GRCh38#125068604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59228993-A-C

125068612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59229000-A-G

125068769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59229126-C-T

125069455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59229598-G-A

125069627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59229762-T-C

125070897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59230105-C-T

http://identifiers.org/hco/8/GRCh38#125071302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59230608-C-A

125073146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59231105-G-T

125073229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59231188-A-G

125073250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59231209-C-T

125073334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231294-T-C

125073437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231450-A-T

125073461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231473-G-A

125073461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231473-G-C

125073461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231473-G-T

125073799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59231871-A-G

125074025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232216-T-A

http://identifiers.org/hco/8/GRCh38#125074040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59232231-C-A

125074551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232628-T-C

125074642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232696-A-G

125074707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232743-T-C

125074712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232748-T-A

http://identifiers.org/hco/8/GRCh38#125074822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59232836-C-A

125074939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59232937-T-C

125075091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59233065-C-T

125075140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233118-A-G

125075140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233118-A-T

125075146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233124-C-T

125075160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233138-G-A

125075160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233138-G-T

http://identifiers.org/hco/8/GRCh38#125075161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59233139-C-A

125075166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59233144-G-T

125076557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235223-T-C

125076558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235224-G-T

125076601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235246-A-G

http://identifiers.org/hco/8/GRCh38#125076612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59235258-C-A

http://identifiers.org/hco/8/GRCh38#125076629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59235275-C-A

125076629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235275-C-T

125076632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235278-T-A

http://identifiers.org/hco/8/GRCh38#125076737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59235365-C-A

125076737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235365-C-T

125076814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235438-G-A

125076814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235438-G-T

125077019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59235628-T-C

http://identifiers.org/hco/8/GRCh38#125077320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59236635-C-A

125077790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237065-A-G

125077791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237066-T-A

125077808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237082-T-C

http://identifiers.org/hco/8/GRCh38#125077909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59237182-A-C

http://identifiers.org/hco/8/GRCh38#125078077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59237308-A-C

125078154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237403-G-C

125078166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237415-A-G

125078395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237676-A-G

125078460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237741-C-T

125078491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59237774-T-C

http://identifiers.org/hco/8/GRCh38#125078659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59237944-A-C

125078790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: 59238064-G-T

125078852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59238126-T-A

125078852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: synonymous variant
orthologous variants: 59238126-T-C

125078923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: stop gained
orthologous variants: 59238197-G-A

125078923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: missense variant
orthologous variants: 59238197-G-C

http://identifiers.org/hco/8/GRCh38#125080680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59238597-A-C

125080789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59238692-T-C

125080896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59238784-A-G

125081127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239022-A-G

125081156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239042-T-A

125081631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239215-T-C

125081898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239473-T-C

125081927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239499-G-A

125082175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239757-T-C

125082229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239814-C-G

http://identifiers.org/hco/8/GRCh38#125082265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59239831-C-A

125082265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron variant
orthologous variants: 59239831-C-T

125082531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59240363-G-A

http://identifiers.org/hco/8/GRCh38#125082566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240399-C-A

125082566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59240399-C-T

http://identifiers.org/hco/8/GRCh38#125082587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240417-C-A

http://identifiers.org/hco/8/GRCh38#125082603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240433-C-A

125082603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59240433-C-G

http://identifiers.org/hco/8/GRCh38#125082843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240788-A-C

125082843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59240788-A-T

125082906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240850-A-G

125082906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240850-A-T

http://identifiers.org/hco/8/GRCh38#125082915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240859-C-A

http://identifiers.org/hco/8/GRCh38#125083040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240936-A-C

125083040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240936-A-G

125083053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240949-T-C

125083069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240960-C-T

125083087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240976-T-A

125083087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240976-T-G

125083093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59240982-A-G

http://identifiers.org/hco/8/GRCh38#125083107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59240996-C-A

125083337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59241364-T-C

125083519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59241534-A-G

125083519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59241534-A-T

http://identifiers.org/hco/8/GRCh38#125083599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59241620-C-A

http://identifiers.org/hco/8/GRCh38#125083705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59241723-A-C

125083818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59241834-A-G

125083881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59241897-G-A

125083887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59241903-A-G

http://identifiers.org/hco/8/GRCh38#125084069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59242074-C-A

125084076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242081-G-A

125084076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242081-G-T

125084649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242453-T-C

125084673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242476-T-C

125084695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242501-C-T

125084705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242515-T-C

125084900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59242924-T-C

125085137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59243447-T-C

125085314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59243617-G-A

http://identifiers.org/hco/8/GRCh38#125085375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59243682-A-C

125090594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59244655-T-C

125090965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59245316-C-G

http://identifiers.org/hco/8/GRCh38#125091090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59245408-A-C

125091446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59245764-G-C

125091585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59245860-A-G

125091662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59245913-G-A

125091706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59245954-G-A

125091706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59245954-G-C

125091736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59245977-A-G

125091797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59246046-G-A

125091797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59246046-G-T