35431878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473329-G-A

35431947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473265-T-C

35431949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473263-C-T

http://identifiers.org/hco/11/GRCh38#35431968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102473249-C-A

35431968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473249-C-G

35431968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473249-C-T

35432006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473212-T-C

http://identifiers.org/hco/11/GRCh38#35432028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102473190-C-A

35432028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473190-C-T

35432060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473143-G-T

35432133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473079-G-A

http://identifiers.org/hco/11/GRCh38#35432143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102473069-C-A

35432143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473069-C-T

http://identifiers.org/hco/11/GRCh38#35432179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102473034-A-C

35432179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473034-A-G

35432179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473034-A-T

http://identifiers.org/hco/11/GRCh38#35432186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102473029-C-A

35432186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473029-C-G

35432186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473029-C-T

35432204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102473011-C-T

http://identifiers.org/hco/11/GRCh38#35432230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102472985-A-C

35432230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102472985-A-G

http://identifiers.org/hco/11/GRCh38#35432296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102472919-C-A

35432296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102472919-C-T

35432312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102472906-G-T

http://identifiers.org/hco/11/GRCh38#35432322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102472895-C-A

35432322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 3 prime UTR variant
orthologous variants: 102472895-C-T

35432420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472799-C-G

35432420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472799-C-T

35432744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472475-T-C

http://identifiers.org/hco/11/GRCh38#35432795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102472424-C-A

35432795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472424-C-T

35432828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472391-A-G

35432852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102472367-A-G

35432958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102472262-G-A

35432958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102472262-G-T

35432979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102472241-G-T

http://identifiers.org/hco/11/GRCh38#35432998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102472228-A-C

35432998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102472228-A-T

35433257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471970-A-T

35433903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471782-G-A

35433936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471750-G-A

35434061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471625-C-G

35434278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471510-T-C

35434285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471502-G-C

35434287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471500-C-T

35434310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471477-C-T

35434319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471468-A-T

35434330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471457-A-T

http://identifiers.org/hco/11/GRCh38#35434346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102471440-C-A

35434378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471407-A-G

35434378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471407-A-T

http://identifiers.org/hco/11/GRCh38#35434384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102471400-C-A

35434384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471400-C-T

http://identifiers.org/hco/11/GRCh38#35434414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102471370-C-A

35434414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471370-C-T

35434415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471369-A-G

35434415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471369-A-T

35434416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471368-T-C

35434416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471368-T-G

35434448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471356-C-G

35434448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471356-C-T

35434462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471342-G-A

http://identifiers.org/hco/11/GRCh38#35434491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102471321-C-A

35434491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102471321-C-T

35434504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 102471310-T-A

http://identifiers.org/hco/11/GRCh38#35434648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102471166-C-A

35434648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102471166-C-T

35434753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 102471061-C-T

http://identifiers.org/hco/11/GRCh38#35434868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102470958-C-A

35434868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470958-C-T

35435143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470366-T-C

35435208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470316-A-G

35435244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470279-C-T

35435279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470247-A-G

35435292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470234-G-A

35435294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102470233-A-T

35435765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102469955-T-G

35435813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102469883-A-T

http://identifiers.org/hco/11/GRCh38#35435846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102469843-C-A

35435846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102469843-C-T

35435853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102469836-A-T

http://identifiers.org/hco/11/GRCh38#35435974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102469715-C-A

35435974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102469715-C-T

35436001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102469688-T-C

35436143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 102469546-A-G

35436247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102469464-A-T

35436316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102469436-G-T

http://identifiers.org/hco/11/GRCh38#35437062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102468841-C-A

35437062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468841-C-T

35437181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468737-T-C

35437296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468614-A-G

35437512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468409-G-A

35437555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468367-G-A

http://identifiers.org/hco/11/GRCh38#35437645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102468324-A-C

35437658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468312-A-T

http://identifiers.org/hco/11/GRCh38#35437666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102468304-C-A

35437743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102468237-G-A

35438538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467669-G-A

35438703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467532-C-T

35438708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467527-A-G

35438828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467356-G-C

35438829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467342-G-A

35438879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467283-C-G

35438948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467212-G-A

35439081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467111-G-A

35439081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102467111-G-C

35439589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466620-T-C

35439599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466610-G-T

35439684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense variant
orthologous variants: 102466526-T-A

35439716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466495-T-G

35439717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466494-G-C

35439717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466494-G-T

35439729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466482-T-C

35439729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466482-T-G

35439739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466472-C-T

35439790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466419-C-G

35439790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466419-C-T

35439810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466399-T-C

http://identifiers.org/hco/11/GRCh38#35439811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102466398-C-A

35439811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466398-C-G

35439811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466398-C-T

35439845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102466366-T-C

35440729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102465519-C-T

35440731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102465517-T-C

http://identifiers.org/hco/11/GRCh38#35440867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102465385-A-C

http://identifiers.org/hco/11/GRCh38#35441040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102465252-A-C

35441147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102465171-C-T

http://identifiers.org/hco/11/GRCh38#35441344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102465007-C-A

35441354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464995-T-C

35441463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464901-G-C

35441769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464589-T-G

http://identifiers.org/hco/11/GRCh38#35441836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102464513-A-C

35442059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464288-G-A

35442086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464261-G-C

35442131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464211-C-T

35442228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102464112-T-G

35442487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102463620-A-T

35442557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102463546-A-G

35450128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102463194-G-A

35450128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102463194-G-T

35450491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462856-C-T

35450588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462778-A-G

35450662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462710-C-T

35450798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462582-T-C

35450799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462581-A-G

35450881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462476-T-C

35451067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462300-T-C

35451184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462185-C-G

35451282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102462107-A-G

35451453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461932-A-T

35451754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461653-A-G

35451768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461639-G-T

http://identifiers.org/hco/11/GRCh38#35451778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102461629-C-A

35451778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461629-C-T

35451800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461607-T-A

35451800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461607-T-C

35451849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102461558-G-T

35451908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102461486-G-A

35451908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102461486-G-T

35451918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102461470-T-C

http://identifiers.org/hco/11/GRCh38#35451969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102461428-C-A

35451969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461428-C-T

35451980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461417-T-C

35452096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461294-C-T

35452180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461199-C-G

35452180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461199-C-T

35452306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102461076-A-G

35452398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460995-T-C

35452412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460981-A-G

35453582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460707-C-G

http://identifiers.org/hco/11/GRCh38#35454024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102460270-A-C

35454027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460267-T-C

35454040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460254-T-C

35454040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460254-T-G

35454133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102460165-A-G

35454358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102459946-T-C

35455004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102459432-A-T

35455205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102459244-T-C

35455384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102459091-T-A

http://identifiers.org/hco/11/GRCh38#35455498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102458969-A-C

http://identifiers.org/hco/11/GRCh38#35455896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102458086-C-A

35456153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102457599-T-C

35456235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102457530-G-T

35456281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102457485-G-T

35456407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102457353-A-G

35456585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102457226-C-T

35458264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102455879-T-C

35458430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102455724-A-T

35458609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102455584-T-C

35459815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102453943-A-G

35459826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102453932-A-G

35459871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102453891-C-T

35459999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102453772-A-G

35460065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102453065-A-G

35460241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102452930-T-C

http://identifiers.org/hco/11/GRCh38#35460243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102452928-A-C

http://identifiers.org/hco/11/GRCh38#35461148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102452821-C-A

35461223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102452748-G-T

35462711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451996-C-T

35462750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451969-T-C

35462838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451890-T-G

35462900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451842-A-G

35462911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451831-T-C

http://identifiers.org/hco/11/GRCh38#35463703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102451014-A-C

35463703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102451014-A-G

35463986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102450789-C-T

http://identifiers.org/hco/11/GRCh38#35464113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102449936-C-A

35464220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102449844-A-G

35464220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102449844-A-T

35464569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102449457-C-T

35464810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448954-A-G

35465055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448759-G-A

35465060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448754-G-A

35465060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448754-G-T

35465465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448457-T-A

35465522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448401-T-C

35465562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448361-G-C

35465581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102448342-G-C

http://identifiers.org/hco/11/GRCh38#35466073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102447743-A-C

35466073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102447743-A-T

http://identifiers.org/hco/11/GRCh38#35466754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102447109-C-A

35466754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102447109-C-G

35466798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102447006-A-T

http://identifiers.org/hco/11/GRCh38#35467117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102446627-C-A

35467233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102446543-C-G

35467906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445366-T-C

http://identifiers.org/hco/11/GRCh38#35467927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102445346-C-A

35467927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445346-C-T

35467989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445298-A-G

http://identifiers.org/hco/11/GRCh38#35468000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102445287-C-A

35468000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 102445287-C-T

http://identifiers.org/hco/11/GRCh38#35468009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102445278-C-A

35468009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102445278-C-T

35468057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102445230-G-A

35468057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102445230-G-T

35468060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102445227-T-A

35468060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102445227-T-C

http://identifiers.org/hco/11/GRCh38#35468121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102445167-A-C

35468121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445167-A-G

http://identifiers.org/hco/11/GRCh38#35468139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102445155-C-A

35468141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445153-A-G

35468264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102445034-C-T

35468412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444880-T-C

35468797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444467-T-C

35468852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444411-C-T

35468963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444316-A-G

35469081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444190-T-A

35469153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444120-G-T

35469262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102444011-G-A

35469502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102443817-G-C

35469537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102443777-A-G

35469767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102443540-G-A

35469948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102443354-A-T

35470242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102442463-A-T

35470480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102442231-T-C

35470486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102442225-G-T

35470591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102442132-T-C

35470615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102442108-T-C

35470759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102441964-C-T

35470768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102441955-A-G

35470777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102441946-T-A

35470777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102441946-T-C

35470806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102441917-C-G

35470847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441877-G-A

35470847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441877-G-T

35472579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441737-A-G

35472728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441589-C-T

35472753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441563-T-C

35472758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441558-G-A

35472806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441510-G-A

35472911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441410-A-G

35472914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441407-A-G

35473017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441301-G-A

35473049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102441272-T-C

35473332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440992-C-T

35473404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440923-G-A

35473426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440901-T-C

35473445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440882-C-T

35473490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440845-C-T

http://identifiers.org/hco/11/GRCh38#35473496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102440839-C-A

35473496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440839-C-G

35473586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440748-T-C

35474607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440342-G-C

35474607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440342-G-T

35474681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102440268-G-T

35474802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440148-G-C

35474874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440081-G-A

35474874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102440081-G-T

35475399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102432748-T-C

35475880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102432036-A-G

http://identifiers.org/hco/11/GRCh38#35475985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102431929-A-C

35476226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102431719-C-T

35476772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102431114-C-T

http://identifiers.org/hco/11/GRCh38#35476817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102431039-C-A

35477059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102430905-G-A

35477169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102430856-T-A

35477662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102430302-T-C

35478650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102429378-C-T

35478823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102429196-T-C

35478851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102429090-T-C

35479037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102428789-C-G

35479049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102428777-C-G

35479774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427792-G-A

http://identifiers.org/hco/11/GRCh38#35479861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102427695-A-C

http://identifiers.org/hco/11/GRCh38#35479869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102427687-C-A

35479898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427660-A-G

35479930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427628-G-A

http://identifiers.org/hco/11/GRCh38#35480027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102427521-C-A

35480196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427361-T-C

35480318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427252-T-C

35480318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427252-T-G

35480450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102427049-T-C

35482879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426847-T-A

35482879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426847-T-C

35482933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426783-T-A

35482972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426746-T-C

35483224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426496-C-T

35483272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426446-C-T

35483329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426397-G-A

35483618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426157-G-A

35483765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426028-T-A

35483781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102426013-C-T

35484383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102425029-G-T

35484389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102425023-G-A

35484516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102424107-C-T

35484518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102424105-T-C

35484551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102424066-T-C

35484716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102423907-A-G

35485040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102421458-C-T

http://identifiers.org/hco/11/GRCh38#35485060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102421442-C-A

35485060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102421442-C-G

35485244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102421132-G-C

35485353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102421039-A-T

http://identifiers.org/hco/11/GRCh38#35485526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102420868-C-A

35485697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420708-T-C

35485766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102420664-C-G

35485812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420619-C-G

35485840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420598-A-G

35485840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420598-A-T

35485860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102420570-G-A

35486024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102420386-T-C

35486167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420262-C-G

35486353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102420070-A-T

35486420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419993-T-G

35486536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419891-T-C

35491058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418312-G-A

35491332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418083-C-G

35491568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417863-G-C

http://identifiers.org/hco/11/GRCh38#35491935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102417182-C-A

35491935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417182-C-T

35491936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417181-T-A

35491936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417181-T-C

35491937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417180-G-A

35491937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417180-G-T

35491967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417150-G-A

35491967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417150-G-C

35491967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417150-G-T

35492081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102417030-C-G

http://identifiers.org/hco/11/GRCh38#35492086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102417025-C-A

35492086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102417025-C-G

35492086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102417025-C-T

http://identifiers.org/hco/11/GRCh38#35492231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102416889-C-A

35492266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416855-T-G

http://identifiers.org/hco/11/GRCh38#35492282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102416840-A-C

35492282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416840-A-T

35492488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416629-G-A

35492810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416036-T-C

35492826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416019-G-T

35493672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411869-G-T

http://identifiers.org/hco/11/GRCh38#35493858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102411493-A-C

35493887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411460-C-T

35493957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411390-G-A

35493957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411390-G-T

http://identifiers.org/hco/11/GRCh38#35493987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102411360-C-A

35493987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411360-C-T

35494054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411294-A-G

http://identifiers.org/hco/11/GRCh38#35494056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102411292-C-A

35494056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411292-C-T

http://identifiers.org/hco/11/GRCh38#35494071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102411277-C-A

http://identifiers.org/hco/11/GRCh38#35494212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102411136-C-A

35494212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102411136-C-T

35494248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102411100-C-T

35494652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411019-T-A

35494746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410928-T-C

35494753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410921-A-G

35494934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410435-T-C

35495098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410263-C-T

35495489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409881-G-C

35495513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409846-T-G

35495516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409843-T-A

35495641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409716-A-G

35495841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409521-T-A

35498756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402566-C-T

35498867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402461-C-T

35499081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401547-G-A

35499081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401547-G-C

35499094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401534-C-T

35499112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401517-C-T

http://identifiers.org/hco/11/GRCh38#35499164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102401457-A-C

35499235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401388-A-G

35499256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401380-T-A

35499462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401189-G-A

35499990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400745-G-A

35500007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400728-T-C

http://identifiers.org/hco/11/GRCh38#35500072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102400673-C-A

35500072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400673-C-T

35500240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400542-C-T

35500453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400334-C-G

35500453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400334-C-T

35500538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400249-A-G

35509247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399733-C-T

35509370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399622-G-A

35509428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399565-G-C

35509476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399517-C-T

35509496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399498-T-C

35509878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102399213-A-G

http://identifiers.org/hco/11/GRCh38#35510504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102398047-A-C

35510748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397807-T-C

http://identifiers.org/hco/11/GRCh38#35510821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102397737-A-C

35511317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397399-C-T

35511578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397127-C-T

35511918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396820-G-A

35512247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396502-C-G

35512387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396353-T-C

35512525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396230-G-C

35512525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396230-G-T

35513145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102395566-G-A

35513284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102395460-T-A

35513338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102395366-G-C

http://identifiers.org/hco/11/GRCh38#35513424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102395297-C-A

http://identifiers.org/hco/11/GRCh38#35513506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102395219-C-A

http://identifiers.org/hco/11/GRCh38#35513550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102395158-C-A

35513550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102395158-C-T

http://identifiers.org/hco/11/GRCh38#35513561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102395147-C-A

http://identifiers.org/hco/11/GRCh38#35513698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102395017-A-C

35513883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394860-G-T

35513884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394859-T-C

35513964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394811-C-T

35514055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394729-T-C

35514130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394653-G-A

35514518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392302-C-G

35514545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392274-C-T

35514740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392137-G-A

35514937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392003-C-G

35515023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391908-C-T

http://identifiers.org/hco/11/GRCh38#35515053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102391878-C-A

35515258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391579-A-G

35515321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391517-A-G

35515697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391167-C-T

35515864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391021-G-C

35516241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389939-T-G

35516543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389599-A-G

35516577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389565-C-T

35516657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389489-G-A

35516663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389483-C-T

35516944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389359-G-A

35516968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389336-G-T

35516985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389311-G-A

35516985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389311-G-C

http://identifiers.org/hco/11/GRCh38#35517177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102389125-C-A

35517402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388924-C-T

35517419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388907-T-G

35517966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388356-C-T

35518040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388284-C-T

35518131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388197-A-G

35518262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388073-A-G

35518440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388907-T-A

35518440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388907-T-G

35518671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387922-A-G

35518977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387631-A-G

35519046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387564-A-G

35519198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387382-G-T

35519505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387092-C-T

35519648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386959-A-T

35519695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386921-C-T

35520540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385638-G-A

35520540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385638-G-C

35520551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385627-G-A

35520614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385570-C-T

http://identifiers.org/hco/11/GRCh38#35521286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102384185-A-C

35523077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102383058-C-T

http://identifiers.org/hco/11/GRCh38#35523101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102383034-A-C

35523247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102382888-C-G

35523915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102382268-T-C

35523964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102382242-T-G

35524076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102382132-G-A

35524277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102381904-A-G

35524820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102381201-C-T

35524830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102381191-T-C

35524923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102381096-G-T

http://identifiers.org/hco/11/GRCh38#35525057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380986-A-C

35525209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102380870-T-G

35525218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102380858-G-C

35525298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102380737-G-A

http://identifiers.org/hco/11/GRCh38#35525397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380662-A-C

35525397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102380662-A-T

http://identifiers.org/hco/11/GRCh38#35525437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380649-C-A

35525456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102380634-G-A

35525577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102380543-C-G

35525626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380489-G-C

35525626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380489-G-T

http://identifiers.org/hco/11/GRCh38#35525665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380443-C-A

35525665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380443-C-G

35525819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102380299-G-A

http://identifiers.org/hco/11/GRCh38#35525835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380283-A-C

35525835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380283-A-G

http://identifiers.org/hco/11/GRCh38#35525836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380282-C-A

35525836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380282-C-G

35525836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 102380282-C-T

35525961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102380144-G-A

35525961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102380144-G-C

35525970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102380134-G-A

35525970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102380134-G-T

http://identifiers.org/hco/11/GRCh38#35525973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102380131-C-A

35526002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102379930-G-A

35526002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 102379930-G-T

35526037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102379895-A-G

35526074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102379858-G-T

35526089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102379723-G-A

35526089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102379723-G-T

http://identifiers.org/hco/11/GRCh38#35526135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102379677-C-A

35526135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: 102379677-C-G

35526135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: 102379677-C-T

http://identifiers.org/hco/11/GRCh38#35526145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102379670-A-C

35526145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: 102379670-A-G

35526145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron_variant, undefined
orthologous variants: 102379670-A-T

35526918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378646-T-C

35527011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378573-T-A

35527087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378498-T-G

35527197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378340-G-T

35527341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378202-A-G

http://identifiers.org/hco/11/GRCh38#35527366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102378192-A-C

35527426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378123-C-T

35527777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102378573-C-T

35528287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102377044-C-T

35528709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102376461-C-T

35528752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102376417-A-T

http://identifiers.org/hco/11/GRCh38#35528898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102376268-C-A

35528938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: intron variant
orthologous variants: 102376229-T-C

35529953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 102375218-G-A

35529988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5 prime UTR variant
orthologous variants: 102375202-A-G

35530125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 102375099-G-A

http://identifiers.org/hco/11/GRCh38#35530129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102375095-C-A

35530129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 102375095-C-T

35530225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 102375002-G-A

35530225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 102375002-G-T

35530262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5 prime UTR variant
orthologous variants: 102374968-G-A

http://identifiers.org/hco/11/GRCh38#35530272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24554
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102374962-C-A