219968750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 185160401-T-C

219968870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185160278-C-T

219968995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185160161-C-T

219969103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185160066-C-T

219969252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159936-G-A

219969252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159936-G-T

http://identifiers.org/hco/1/GRCh38#219969257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185159931-C-A

219969257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159931-C-T

http://identifiers.org/hco/1/GRCh38#219969266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185159922-C-A

219969266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159922-C-T

http://identifiers.org/hco/1/GRCh38#219969267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185159921-C-A

219969267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159921-C-G

219969267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159921-C-T

219969268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159920-T-A

219969268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159920-T-G

219969329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159855-T-A

219969329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159855-T-C

http://identifiers.org/hco/1/GRCh38#219969361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185159837-C-A

219969362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159836-A-G

219969362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159836-A-T

219969393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185159805-C-T

http://identifiers.org/hco/1/GRCh38#219969700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185159539-C-A

219970963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185157044-A-G

219971014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185157015-A-T

219971134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156916-T-C

http://identifiers.org/hco/1/GRCh38#219972003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185156714-C-A

219972003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156714-C-T

219972028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156689-T-A

219972028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156689-T-C

http://identifiers.org/hco/1/GRCh38#219972046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185156630-A-C

219972046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156630-A-G

219972181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156475-G-A

219972181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156475-G-C

219972181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156475-G-T

219972202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156450-T-G

219972204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156448-T-G

219972285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156380-C-T

http://identifiers.org/hco/1/GRCh38#219972286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185156379-A-C

219972286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156379-A-G

219972286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156379-A-T

219972289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156376-G-C

219972289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156376-G-T

219972329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185156342-T-C

219972838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185152845-A-G

219972884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185152799-G-A

http://identifiers.org/hco/1/GRCh38#219972945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185152739-A-C

219973226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185152493-T-A

219973459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185152266-G-A

219973459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185152266-G-T

http://identifiers.org/hco/1/GRCh38#219977501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185151533-A-C

219977729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185151383-G-A

219977839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185151282-G-C

219978114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150993-T-C

http://identifiers.org/hco/1/GRCh38#219978441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185150643-A-C

219978441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150643-A-T

219978536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150588-A-G

219978536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150588-A-T

219978643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense variant
orthologous variants: 185150483-T-A

http://identifiers.org/hco/1/GRCh38#219978712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185150414-A-C

http://identifiers.org/hco/1/GRCh38#219978734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185150379-A-C

219978734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150379-A-G

219978735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150378-T-C

219978735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150378-T-G

219978748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150365-T-C

219978748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150365-T-G

219978769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150335-G-A

219978769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185150335-G-T

219979209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185148329-A-G

219979638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185147930-A-G

219979638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185147930-A-T

http://identifiers.org/hco/1/GRCh38#219979706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185147866-C-A

219980026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146734-G-A

219980026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146734-G-T

219980027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146733-G-A

219980027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146733-G-C

219980027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146733-G-T

219980031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146729-T-C

http://identifiers.org/hco/1/GRCh38#219980385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185146411-C-A

219980385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146411-C-T

219980438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185146365-A-G

219980665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145824-A-T

219980672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145817-G-A

219980672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145817-G-C

219980672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145817-G-T

219980865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 185145636-A-G

219980865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 185145636-A-T

219980888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145614-T-A

http://identifiers.org/hco/1/GRCh38#219981281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185145521-C-A

219981281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145521-C-T

219981312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145499-T-A

219981312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145499-T-C

219981312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145499-T-G

219981332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145474-A-G

219981332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145474-A-T

219981363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145443-G-A

219981363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145443-G-C

219981363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145443-G-T

219981406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense variant
orthologous variants: 185145401-A-G

219981508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145305-T-C

219981609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145243-A-G

219981667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145178-A-G

219981802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185145064-C-T

219982471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185144437-A-G

http://identifiers.org/hco/1/GRCh38#219982476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185144432-A-C

http://identifiers.org/hco/1/GRCh38#219982582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185144305-C-A

219982582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144305-C-G

219982582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144305-C-T

219982631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144239-T-C

http://identifiers.org/hco/1/GRCh38#219982637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185144233-C-A

219982637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144233-C-G

219982637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144233-C-T

219982738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144003-G-A

219982738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185144003-G-T

219982885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143857-G-T

219982957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143799-G-C

219982957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143799-G-T

219983078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143698-T-G

219983232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185143519-G-A

219983462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143300-G-A

219983462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143300-G-C

219983462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143300-G-T

219983524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143159-G-C

219983570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143067-A-T

219983597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185143022-T-C

219983668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185142882-G-T

219983700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185142829-C-T

219983733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185142803-A-G

219983734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185142802-A-G

http://identifiers.org/hco/1/GRCh38#219984103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185142534-C-A

219984170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185142466-A-G

219986099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185140999-G-C

219987094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185139976-G-A

219987094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185139976-G-T

219988710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: synonymous variant
orthologous variants: 185139269-T-C

219988750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense variant
orthologous variants: 185139229-T-C

219988801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense variant
orthologous variants: 185139178-T-C

219988837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185139143-G-C

219988837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185139143-G-T

219988866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185139121-A-T

http://identifiers.org/hco/1/GRCh38#219988942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185139026-C-A

219989586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185138355-G-A

219989606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185138335-A-G

219989665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185138268-T-A

219989679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185138254-C-T

219996893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185133931-A-G

219996893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185133931-A-T

219996956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron variant
orthologous variants: 185133880-G-A

219997275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185133571-G-A

219997275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185133571-G-C

219997389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185133459-T-C

219997419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185133431-T-A

219997419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185133431-T-G

220001092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 185131565-T-C

220001217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185131455-T-C

220001341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185131337-A-G

220005057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130949-G-A

220005131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130893-A-G

220005131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130893-A-T

220005132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130892-G-T

220005196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130838-A-G

220005233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130782-G-A

220005233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130782-G-T

220005257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185130692-T-C

220005269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185130680-T-C

220005320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185130629-A-G

220005371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130579-G-A

220005371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130579-G-T

220005383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130567-A-G

http://identifiers.org/hco/1/GRCh38#220005387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185130563-C-A

220005390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130560-T-C

220005402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130550-A-G

220005458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130495-T-C

220005532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130196-A-G

220005599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130130-T-C

220005616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185130113-T-C

220005807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129968-T-A

220005807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129968-T-C

220005827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129947-T-G

220005844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129929-T-A

220005852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129921-T-C

220006055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129509-A-G

220006055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129509-A-T

220006170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185129398-A-G

220006201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185129367-T-C

220006308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185129260-G-A

220006308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 185129260-G-T

220006317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 185129253-G-T

220006331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129238-A-G

220006339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129230-A-G

http://identifiers.org/hco/1/GRCh38#220006429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185129185-A-C

220006539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185129076-C-T

220006719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185128901-T-G

220006861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185128769-T-G

220007037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185128564-T-C

220007116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 185128437-G-T

220007362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 185128201-T-C

http://identifiers.org/hco/1/GRCh38#220011083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185126535-A-C

220011089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126529-G-T

220011102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126518-G-A

220011104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126516-G-A

220011104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126516-G-T

220011132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126488-A-G

220011365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126229-G-C

220011414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126183-T-C

220011460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126138-T-C

220011470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126126-T-G

220011526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126082-T-C

220011559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185126049-A-G

220011675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185125869-T-C

220018213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119488-C-G

220018213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119488-C-T

http://identifiers.org/hco/1/GRCh38#220018551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185119138-A-C

220018551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119138-A-G

220018625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119059-T-A

220018640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119045-T-A

220018640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185119045-T-C

220018845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118668-T-A

220018845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118668-T-C

220018845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118668-T-G

220018876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118641-G-A

220018876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118641-G-T

220019094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118425-A-G

220019094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118425-A-T

http://identifiers.org/hco/1/GRCh38#220019134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185118391-A-C

220019137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185118388-G-T

http://identifiers.org/hco/1/GRCh38#220019180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185118343-A-C

http://identifiers.org/hco/1/GRCh38#220019537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185117968-A-C

220019601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185117742-C-G

220019685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185117599-C-T

http://identifiers.org/hco/1/GRCh38#220019890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185117370-C-A

220019890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185117370-C-T

http://identifiers.org/hco/1/GRCh38#220019891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185117369-C-A

220019891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185117369-C-T

http://identifiers.org/hco/1/GRCh38#220019904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185117356-C-A

220019904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185117356-C-T

220020096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 185117197-C-T

220020108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 185117185-A-G

220020192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 185117101-G-A

220020525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185116331-A-G

220022115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185114385-A-G

220022241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185114279-A-G

220022245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185114275-A-G

220022279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185114239-C-T

http://identifiers.org/hco/1/GRCh38#220022292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185114210-A-C

220022292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185114210-A-G

220022398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 185114115-G-T

220022625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113931-C-G

220022755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113740-A-G

220022819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113707-C-G

220022931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113596-C-T

220022959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113568-C-T

220023069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113531-C-G

220023394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185113220-C-T

http://identifiers.org/hco/1/GRCh38#220023448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185113164-C-A

220023570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185112446-A-G

220023571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185112445-T-C

220023588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185112428-C-T

http://identifiers.org/hco/1/GRCh38#220024220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185111978-A-C

220024224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111974-T-A

220024224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111974-T-C

220024224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111974-T-G

220024258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111938-G-A

220024258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111938-G-T

220024434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 185111762-A-G

220024459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 185111737-G-A

220024459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 185111737-G-T

220024494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111688-T-G

220024506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111676-G-A

220024506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111676-G-C

220024506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111676-G-T

220024512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111670-T-A

220024523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111659-G-T

220024569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111613-G-T

http://identifiers.org/hco/1/GRCh38#220024570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185111612-C-A

220024570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111612-C-T

220024573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111609-G-A

220024573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111609-G-T

http://identifiers.org/hco/1/GRCh38#220024711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185111487-C-A

220024945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111282-A-G

220024945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185111282-A-T

http://identifiers.org/hco/1/GRCh38#220025311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185110917-C-A

220025311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110917-C-T

http://identifiers.org/hco/1/GRCh38#220025370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185110865-C-A

220025377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110860-T-A

220025377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110860-T-C

220025455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110789-T-A

220025455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110789-T-C

220025501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110748-G-C

220025521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110729-T-C

220025671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185110592-A-G

220028385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185109015-G-A

220028434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185108970-C-T

220028734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185108689-T-C

http://identifiers.org/hco/1/GRCh38#220029402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185107340-A-C

220029419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185107323-G-A

220029687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185107008-T-C

220029750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106943-T-C

220029800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106895-T-C

http://identifiers.org/hco/1/GRCh38#220030262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185106515-C-A

220030262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106515-C-T

220030509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106288-A-G

http://identifiers.org/hco/1/GRCh38#220030531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185106266-A-C

220030531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106266-A-G

http://identifiers.org/hco/1/GRCh38#220030604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185106214-C-A

220030620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106197-G-A

220030620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185106197-G-T

220032398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185105241-T-C

220032537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185105102-A-G

220032587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185105052-A-G

http://identifiers.org/hco/1/GRCh38#220032603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185105036-A-C

220032624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185105014-T-C

http://identifiers.org/hco/1/GRCh38#220033046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185103991-A-C

220033046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103991-A-G

220033091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103947-C-T

220033363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103730-T-C

220033418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103674-T-C

220033418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103674-T-G

http://identifiers.org/hco/1/GRCh38#220033426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185103669-C-A

220033426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103669-C-T

220033608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 185103134-G-C

220033677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103067-G-A

220033677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103067-G-C

220033677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103067-G-T

http://identifiers.org/hco/1/GRCh38#220033689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185103055-A-C

220033699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185103045-T-C

220033766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102968-T-C

220033787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102947-T-C

220033852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102883-G-A

220033853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102882-C-T

220033879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102849-C-T

220033913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102810-C-T

220033916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102807-C-T

220033923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102800-G-T

220034008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102727-T-A

http://identifiers.org/hco/1/GRCh38#220034051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185102683-C-A

220034058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102676-C-T

220034458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102449-G-C

220034541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102380-G-A

220034623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102297-C-T

http://identifiers.org/hco/1/GRCh38#220034632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185102288-C-A

220034632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102288-C-G

220034662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185102258-G-A

http://identifiers.org/hco/1/GRCh38#220034798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185101987-C-A

220034798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101987-C-T

http://identifiers.org/hco/1/GRCh38#220034807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185101978-A-C

220034807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101978-A-T

220034894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101891-A-G

220034896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101889-A-G

220034905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101880-A-G

220034930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101855-A-G

220034950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 185101835-A-G

220034951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101834-G-C

220034951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101834-G-T

220034969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101816-G-A

220034969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101816-G-T

220034993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185101792-A-G

http://identifiers.org/hco/1/GRCh38#220035139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185101658-A-C

220035139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185101658-A-G

http://identifiers.org/hco/1/GRCh38#220040254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185099741-A-C

220040254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185099741-A-G

220040254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 185099741-A-T

220040281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185099711-A-G

220040281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185099711-A-T

http://identifiers.org/hco/1/GRCh38#220040338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185099658-C-A

220040474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185099525-A-G

220042973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185098422-C-T

220043685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185097464-T-G

220043699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185097450-A-G

220043960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185097215-A-T

220044234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096957-A-G

220044284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096913-G-A

http://identifiers.org/hco/1/GRCh38#220044732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185096623-C-A

220044839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096553-T-A

220044854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096539-G-C

220045292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096296-T-G

220045328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096277-C-T

220045376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096238-C-T

220045397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096216-A-G

http://identifiers.org/hco/1/GRCh38#220045460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185096176-C-A

220045579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185096070-T-C

http://identifiers.org/hco/1/GRCh38#220045719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#185095952-C-A

220045719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095952-C-T

220045846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095832-G-C

220045888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095796-T-C

220046076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095678-G-T

220046088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095666-C-G

220046093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095661-T-C

220046093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095661-T-G

220046209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 185095531-T-G

http://identifiers.org/hco/1/GRCh38#220046216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185095524-C-A

220046216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 185095524-C-T

220046225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095515-G-A

220046225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 185095515-G-T

220046400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 185095381-C-T

220046496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 185095294-C-G

220046496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 185095294-C-T

http://identifiers.org/hco/1/GRCh38#220046515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#185095274-C-A

220046515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 185095274-C-T

220046524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3418
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 185095265-A-T