53284021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30248400-A-G

http://identifiers.org/hco/3/GRCh38#53284058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30248385-C-A

http://identifiers.org/hco/3/GRCh38#53284096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30248348-C-A

http://identifiers.org/hco/3/GRCh38#53284159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30248286-C-A

53284159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30248286-C-G

53284159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30248286-C-T

53284239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30248211-T-C

http://identifiers.org/hco/3/GRCh38#53284437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30248010-A-C

http://identifiers.org/hco/3/GRCh38#53284444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30248003-C-A

53284453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247993-G-T

http://identifiers.org/hco/3/GRCh38#53284827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30247894-C-A

53284854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247867-T-G

http://identifiers.org/hco/3/GRCh38#53284906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30247816-A-C

53285008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247727-C-T

http://identifiers.org/hco/3/GRCh38#53285045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30247693-A-C

53285204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247537-T-A

53285204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247537-T-C

53285263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247493-A-G

http://identifiers.org/hco/3/GRCh38#53285275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30247481-C-A

53285475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247279-T-C

53285519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247235-G-A

53285542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30247210-T-C

53285795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30246938-T-C

53285800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30246933-A-T

53286201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30246539-C-T

http://identifiers.org/hco/3/GRCh38#53286855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30245876-C-A

http://identifiers.org/hco/3/GRCh38#53286897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30245842-C-A

53287070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30245678-G-T

53287189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30245597-G-A

53287189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30245597-G-T

53287286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30245511-C-T

53287318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30245479-A-G

53287407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30245412-A-G

53287480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30245359-T-C

53287545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30245296-G-A

53287545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30245296-G-T

53287902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244987-G-A

53287902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244987-G-T

53288025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244939-A-G

53288033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244933-A-G

53288048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244918-A-G

53288130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 30244836-G-A

53288164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30244802-G-C

53288189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30244777-G-A

53288243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30244723-A-G

53290129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244322-G-A

53290213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244264-G-A

53290254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244215-G-A

53290275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244203-G-T

53290310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244171-G-A

53290454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30244019-G-A

53290490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30243986-G-A

53290490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30243986-G-T

53290631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30243845-G-A

53290631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30243845-G-T

53290634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30243842-A-G

http://identifiers.org/hco/3/GRCh38#53292316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30241382-A-C

53292345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30241353-A-G

53292485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30241216-G-C

53292544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30241157-T-C

53292769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30240932-G-A

53292769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30240932-G-C

53292862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30240838-T-C

53292932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30240774-G-T

53293155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30240562-G-A

53293214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30240519-T-C

53293256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30240485-T-C

53293300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30240446-C-T

53303678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235474-G-A

53303678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235474-G-C

53304007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235227-C-G

53304069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235162-C-T

53304116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235113-A-G

53304171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron variant
orthologous variants: 30235058-A-G

53304199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: intron_variant, missense_variant
orthologous variants: 30235030-A-G

53304367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234865-G-T

53304371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234861-A-G

53304371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234861-A-T

53304387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234845-T-C

53304406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234826-A-G

53304454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30234780-T-A

http://identifiers.org/hco/3/GRCh38#53304541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30234694-A-C

53307821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231885-G-T

53307984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231686-G-A

53308030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231638-G-C

53308061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231606-C-T

53308219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231455-G-C

53309004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30231398-G-A

53309854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30230981-G-A

53309854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30230981-G-C

53310093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30230767-C-T

53310754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229549-G-A

53310754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229549-G-T

53310804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229500-A-G

53311008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229355-G-C

53311045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229326-C-T

53311064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30229309-G-T

53311466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30228341-T-G

53311474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30228333-C-T

53311475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30228332-G-A

53311475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30228332-G-T

53311845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227832-T-C

53311935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227759-T-C

53312094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227720-A-G

53312094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227720-A-T

http://identifiers.org/hco/3/GRCh38#53312187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30227681-C-A

53312187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227681-C-G

53312187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227681-C-T

53312230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227650-G-A

53312230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227650-G-C

53312262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 30227618-T-G

53312290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 30227590-G-A

53312290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 30227590-G-T

53312405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227476-A-G

http://identifiers.org/hco/3/GRCh38#53312424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30227459-A-C

53312435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227448-G-A

53312435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227448-G-T

53312820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30227384-A-G

53317841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30225880-C-G

53317965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30225750-C-G

53318510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30225587-C-T

53319033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30225163-T-C

53319075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30225128-A-G

53319314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30224933-A-T

53319577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30224706-A-T

53321157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30220317-G-T

http://identifiers.org/hco/3/GRCh38#53322601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30218114-C-A

53323240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 30217906-T-C

53323585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30217639-C-T

http://identifiers.org/hco/3/GRCh38#53323919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30217569-C-A

http://identifiers.org/hco/3/GRCh38#53324331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30217182-C-A

53324331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30217182-C-T

53324718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30216810-T-C

53324729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30216799-T-C

53325015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30216667-T-A

53325352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30216354-T-C

53325373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30216333-G-A

53325558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30215634-A-G

53326003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30215290-G-A

http://identifiers.org/hco/3/GRCh38#53326940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30215191-A-C

53326949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30215182-G-A

53327153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30214966-G-T

53327321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30214699-A-G

53327527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30214522-C-T

53328907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30213457-T-C

53329191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30213170-C-T

53329213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 30213152-A-G

53329408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 30212960-G-T

http://identifiers.org/hco/3/GRCh38#53329474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30212909-A-C

53329474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30212909-A-G

53329759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30212648-C-T

http://identifiers.org/hco/3/GRCh38#53329767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30212640-A-C

53329972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30212477-G-C

53330098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30212357-T-C

http://identifiers.org/hco/3/GRCh38#53330218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30212235-C-A

53330585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30212009-T-C

53330686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30211905-T-G

53332338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30211556-T-A

53332338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30211556-T-C

53337332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30210373-C-G

53337421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30210303-T-C

53337520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30210211-G-C

53337703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30210064-C-T

53337986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30209793-A-G

53338023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30209764-A-G

53338104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 30209699-G-A

53338104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 30209699-G-T

53338135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 30209671-G-A

53338135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 30209671-G-T

53338153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 30209657-T-C

53338153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 30209657-T-G

http://identifiers.org/hco/3/GRCh38#53338194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30209612-C-A

53338194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30209612-C-T

53338905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30209375-T-A

http://identifiers.org/hco/3/GRCh38#53339265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30209021-C-A

53339265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30209021-C-G

53339460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30208875-A-G

53339562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30208776-T-C

53339612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30208727-A-G

53340365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30208110-T-C

53341008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30207165-C-T

53341013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30207160-C-T

53341530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30207048-G-C

53341574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30207007-T-C

53341994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30206657-A-G

53342313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30206378-T-A

53342379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30206323-T-C

53342702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205957-T-C

53342841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205874-T-A

53342843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205872-T-C

53342929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205631-T-A

53343082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205488-T-C

53343250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30205339-T-C

53344003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204961-T-G

http://identifiers.org/hco/3/GRCh38#53344012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30204952-A-C

53344187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204803-C-G

53344476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204554-G-C

53344587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204453-A-T

53344591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204449-T-C

53344621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204416-G-T

53344638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204405-G-A

53344734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204353-C-T

http://identifiers.org/hco/3/GRCh38#53344771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30204316-C-A

53344771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204316-C-G

53344771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204316-C-T

53344850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204242-A-G

53344862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204225-T-G

53344880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204212-T-C

http://identifiers.org/hco/3/GRCh38#53345000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30204092-C-A

53345000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204092-C-G

53345011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204080-A-G

53345041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30204056-T-C

53345074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30203732-G-T

53345075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30203731-A-G

53345511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30202764-T-A

http://identifiers.org/hco/3/GRCh38#53346888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30202227-A-C

http://identifiers.org/hco/3/GRCh38#53347022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30202124-C-A

53347246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 30201915-G-T

http://identifiers.org/hco/3/GRCh38#53347302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30201859-C-A

53347302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201859-C-G

53347302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201859-C-T

53347350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201805-G-A

53347350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201805-G-T

53347358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201796-G-A

53347358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 30201796-G-T

53347474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 30201680-G-A

53347556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 30201598-G-A

53347556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18714
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 30201598-G-C