219550734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75462481-G-A

http://identifiers.org/hco/2/GRCh38#219550790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75462552-C-A

219550790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75462552-C-T

219550823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75462585-G-T

219550874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75462637-G-A

219550884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462647-G-T

219551169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462912-G-A

219551169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462912-G-T

219551186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462929-G-T

219551207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462949-G-A

219551207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462949-G-T

219551211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75462953-G-A

219551318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463062-G-A

219551342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463073-G-T

http://identifiers.org/hco/2/GRCh38#219551389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463121-C-A

219551389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463121-C-T

http://identifiers.org/hco/2/GRCh38#219551405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463132-C-A

219551405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463132-C-T

http://identifiers.org/hco/2/GRCh38#219551425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463152-C-A

219551425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463152-C-G

219551425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463152-C-T

219551445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463181-G-A

219551445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463181-G-C

219551445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463181-G-T

219551470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463206-A-G

219551470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75463206-A-T

219551638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75463393-G-A

http://identifiers.org/hco/2/GRCh38#219551645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463400-A-C

219551842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463592-G-A

219551842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463592-G-T

http://identifiers.org/hco/2/GRCh38#219551999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463759-C-A

219551999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463759-C-G

219551999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463759-C-T

http://identifiers.org/hco/2/GRCh38#219552099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75463854-C-A

219552099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463854-C-T

219552219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75463975-G-A

219552219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75463975-G-T

http://identifiers.org/hco/2/GRCh38#219552327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75464078-C-A

219552327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75464078-C-G

219552327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75464078-C-T

219552389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75464133-G-A

219552389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75464133-G-C

219552389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75464133-G-T

219552403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464147-C-G

219552403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464147-C-T

http://identifiers.org/hco/2/GRCh38#219552453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75464189-C-A

219552453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464189-C-G

219552453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464189-C-T

219552604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464341-G-C

219552604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464341-G-T

219552641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464378-C-G

219552641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464378-C-T

http://identifiers.org/hco/2/GRCh38#219552684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75464421-C-A

219552684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75464421-C-G

219552684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75464421-C-T

219552768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75464500-C-G

219552768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75464500-C-T

219552889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464571-G-A

219552889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464571-G-T

219552913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75464595-C-T

http://identifiers.org/hco/2/GRCh38#219552989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75464671-C-A

219552989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75464671-C-T

219553157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464840-G-A

219553157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464840-G-T

219553270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464958-G-A

219553502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465176-G-T

219553615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75465274-A-G

http://identifiers.org/hco/2/GRCh38#219553778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75465460-C-A

219553778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465460-C-T

219553813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465495-G-A

219553813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465495-G-C

219553813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465495-G-T

219554035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465717-T-C

219554114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465821-A-G

219554114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465821-A-T

219554151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465867-G-A

219554151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465867-G-C

219554151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465867-G-T

219554201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465916-A-G

219554221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465936-A-T

219554225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465940-A-G

219554239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75465957-A-G

219554268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75465981-G-T

http://identifiers.org/hco/2/GRCh38#219554296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466001-C-A

http://identifiers.org/hco/2/GRCh38#219554303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466009-C-A

219554303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75466009-C-T

219554311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75466017-G-A

219554311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75466017-G-T

http://identifiers.org/hco/2/GRCh38#219554328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466035-A-C

http://identifiers.org/hco/2/GRCh38#219554389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466066-C-A

219554618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 75466271-G-A

219554618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75466271-G-C

219554808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466453-T-A

219554808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466453-T-C

http://identifiers.org/hco/2/GRCh38#219554814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466461-C-A

219554814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466461-C-T

http://identifiers.org/hco/2/GRCh38#219554824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466471-C-A

219554824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466471-C-T

http://identifiers.org/hco/2/GRCh38#219554829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466476-A-C

219554831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466478-C-T

219554837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466483-A-G

219554850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466496-G-T

219554866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466512-G-T

219554880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466524-T-G

219554887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466529-A-G

219554887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466529-A-T

219555048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466606-G-A

219555048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466606-G-T

http://identifiers.org/hco/2/GRCh38#219555064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466622-C-A

219555064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466622-C-G

219555064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466622-C-T

http://identifiers.org/hco/2/GRCh38#219555123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466691-C-A

http://identifiers.org/hco/2/GRCh38#219555132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75466700-C-A

219555132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466700-C-T

219555514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75466999-A-T

http://identifiers.org/hco/2/GRCh38#219555539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75467026-C-A

219555555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467035-T-A

219555557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467037-G-T

http://identifiers.org/hco/2/GRCh38#219555559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75467039-C-A

219555559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467039-C-T

219555560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467040-G-A

219555560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467040-G-C

219555560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467040-G-T

219555678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467137-G-A

219555678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467137-G-T

219555798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467222-G-A

219555798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467222-G-T

219555867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467282-G-A

219555867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467282-G-T

219555886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467304-G-A

219555957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75467395-G-A

219556063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75467483-G-A

219556063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75467483-G-C

219556095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75467515-C-G

219556095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75467515-C-T

219556195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75467615-C-T

219556249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75467669-T-G

http://identifiers.org/hco/2/GRCh38#219556253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75467673-C-A

219556253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75467673-C-T

219556445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75467823-G-C

219556496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75467874-G-A

219556496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75467874-G-T

219556539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75467917-G-A

219556626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75468004-G-A

219556626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75468004-G-T

219556690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75468068-G-A

http://identifiers.org/hco/2/GRCh38#219556802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75468198-C-A

219556802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468198-C-G

219556802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468198-C-T

http://identifiers.org/hco/2/GRCh38#219556850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75468247-A-C

219556850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468247-A-G

219556878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468276-A-G

219556878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468276-A-T

http://identifiers.org/hco/2/GRCh38#219556927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75468322-C-A

219556927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468322-C-G

219556927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75468322-C-T

219557216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468597-T-A

219557216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468597-T-C

219557426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75468794-A-G

http://identifiers.org/hco/2/GRCh38#219557611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75468979-A-C

219557611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75468979-A-G

219557611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75468979-A-T

219557666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469022-T-C

219557722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469063-G-A

219557722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469063-G-T

219557731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469072-G-A

219557731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469072-G-T

219557868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75469195-C-T

219557920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75469247-G-T

219557966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75469293-C-T

219558136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469466-C-T

http://identifiers.org/hco/2/GRCh38#219558434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75469764-C-A

219558434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75469764-C-G

219558434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75469764-C-T

http://identifiers.org/hco/2/GRCh38#219558449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75469779-C-A

219558449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75469779-C-G

219558471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469801-G-A

219558471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469801-G-T

219558504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469834-G-A

219558504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469834-G-T

219558794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469968-A-G

http://identifiers.org/hco/2/GRCh38#219559034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470234-A-C

219559034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470234-A-G

219559034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470234-A-T

219559055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470255-A-G

219559107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470306-T-G

219559137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470335-A-G

219559137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470335-A-T

219559147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470351-G-A

219559147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470351-G-T

219559279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470483-C-G

219559279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470483-C-T

219559318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470522-G-A

219559318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470522-G-T

http://identifiers.org/hco/2/GRCh38#219559364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470568-C-A

219559364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75470568-C-T

219559373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75470577-C-G

219559373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75470577-C-T

219559451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75470655-G-A

219559451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75470655-G-T

219559486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470690-G-A

219559486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75470690-G-C

http://identifiers.org/hco/2/GRCh38#219559583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470769-C-A

http://identifiers.org/hco/2/GRCh38#219559621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470814-C-A

219559621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75470814-C-G

219559636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470829-A-G

219559637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470830-G-T

http://identifiers.org/hco/2/GRCh38#219559654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470846-C-A

219559654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470846-C-T

http://identifiers.org/hco/2/GRCh38#219559662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470854-C-A

219559662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470854-C-T

219559721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470910-A-G

http://identifiers.org/hco/2/GRCh38#219559729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75470918-C-A

219559729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470918-C-T

219559738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470929-G-C

219559738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470929-G-T

219559760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470949-T-C

219559763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470952-T-A

219559841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75471027-T-C

219559900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75471236-A-G

219559908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75471244-C-T

219560097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75471570-A-G

219560131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75471603-C-T

http://identifiers.org/hco/2/GRCh38#219560485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#75471960-A-C

219560821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75472183-T-G

http://identifiers.org/hco/2/GRCh38#219560920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75472234-C-A

http://identifiers.org/hco/2/GRCh38#219561083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75472368-C-A

219561223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75472491-T-C

219561386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75472645-G-A

219561401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75472659-C-T

219561843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75473104-T-G

219561961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75473221-C-T

219562025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473285-G-A

219562025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473285-G-T

219562240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473481-C-G

219562259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473500-G-A

219562259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473500-G-T

http://identifiers.org/hco/2/GRCh38#219562323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75473567-C-A

219562323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473567-C-T

219562624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75473874-C-G

219562624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75473874-C-T

219562664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75473914-C-T

219562727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75473987-T-C

219562793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75474052-G-A

219562793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75474052-G-C

219562793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75474052-G-T

219562810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75474084-G-A

219562810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75474084-G-T

219562833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474109-G-C

219562833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474109-G-T

219562846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474119-A-G

http://identifiers.org/hco/2/GRCh38#219562862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75474135-C-A

219562862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474135-C-T

219562900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474168-A-G

http://identifiers.org/hco/2/GRCh38#219562901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75474169-C-A

219562901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474169-C-G

219562903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474171-A-G

219562944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474212-G-A

219562944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474212-G-C

219562944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474212-G-T

219562968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474248-G-A

219562968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474248-G-T

219563045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474515-C-T

http://identifiers.org/hco/2/GRCh38#219563095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75474548-C-A

http://identifiers.org/hco/2/GRCh38#219563259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75474674-C-A

219563259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474674-C-G

219563259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474674-C-T

219563261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474676-G-A

219563261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474676-G-T

219563278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474693-A-G

219563278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474693-A-T

219563284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474699-G-A

219563284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474699-G-C

219563284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474699-G-T

219563371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75474735-G-C

http://identifiers.org/hco/2/GRCh38#219563386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75474750-A-C

219563386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75474750-A-G

219563433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75474797-C-T

219563569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75474933-G-A

219563652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475013-T-G

http://identifiers.org/hco/2/GRCh38#219563670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75475030-C-A

219563670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475030-C-T

219563711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475047-C-G

219563711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475047-C-T

219563728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475068-G-A

219563728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475068-G-T

219563730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475070-A-G

219563734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475074-G-A

219563735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475075-G-A

219563789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75475127-C-T

219564417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75476116-C-T

219564491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75476175-G-A

219564496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75476180-T-C

219564572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75476250-T-C

http://identifiers.org/hco/2/GRCh38#219565192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75476500-C-A

219565192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75476500-C-T

219565438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75476742-A-G

219565438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75476742-A-T

219565456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75476760-T-G

219565511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75476815-C-T

219565559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75476892-T-A

219565559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75476892-T-C

219565603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75476961-G-C

219565603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75476961-G-T

219565605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75476963-G-T

219566450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75478182-C-G

219566572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75478323-T-C

http://identifiers.org/hco/2/GRCh38#219566749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75478525-A-C

219566759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75478535-T-C

219566769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75478545-T-C

219566769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75478545-T-G

http://identifiers.org/hco/2/GRCh38#219566846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75478619-A-C

219566879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75478652-G-A

219566879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75478652-G-T

219567083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75478856-T-A

219567083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75478856-T-C

219567083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75478856-T-G

219567189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479453-G-A

219567189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479453-G-T

219567203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479458-T-A

219567203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479458-T-G

219567223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479478-G-A

219567223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479478-G-T

219567306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75479590-G-T

219567316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75479600-A-G

219567376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75479660-C-T

219567388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75479672-G-A

219567394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75479678-G-A

219567603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479888-G-T

219567642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479928-A-G

219567684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75479971-T-C

219567851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75480144-C-T

http://identifiers.org/hco/2/GRCh38#219567975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75480268-A-C

219567975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75480268-A-G

219567975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75480268-A-T

219567989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480282-C-G

219568004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480297-C-G

219568025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480312-C-T

http://identifiers.org/hco/2/GRCh38#219568104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75480390-C-A

219568119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75480405-A-G

219568339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480625-G-A

219568339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480625-G-T

219568353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480631-A-G

219568392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480667-A-G

219568396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480671-G-A

219568396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480671-G-T

219568629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480841-A-G

219568648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75480846-C-T

219569142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480999-G-A

219569533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481337-T-A

219569533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481337-T-C

219569579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481376-G-A

219569579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481376-G-C

219569579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481376-G-T

http://identifiers.org/hco/2/GRCh38#219570148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75481801-C-A

219570148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481801-C-G

219570148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75481801-C-T

219570202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481848-G-T

219570285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75481921-G-A

219570285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75481921-G-C

219570423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75482059-C-G

219570501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482137-C-T

http://identifiers.org/hco/2/GRCh38#219570642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#75482278-C-A

219570642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 75482278-C-G

219570642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 75482278-C-T

http://identifiers.org/hco/2/GRCh38#219570921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75482557-C-A

219570921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482557-C-T

219570929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482565-G-A

219570929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75482565-G-C

219570929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75482565-G-T

219570942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482578-G-A

219570942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482578-G-T

219570960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482596-G-A

219570960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482596-G-C

219570960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482596-G-T

http://identifiers.org/hco/2/GRCh38#219571113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75482749-C-A

219571113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482749-C-G

219571113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482749-C-T

http://identifiers.org/hco/2/GRCh38#219571179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75482815-C-A

219571179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75482815-C-T

219571303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75482910-C-T

http://identifiers.org/hco/2/GRCh38#219571446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#75483028-C-A

219571446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75483028-C-G

219571446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75483028-C-T

http://identifiers.org/hco/2/GRCh38#219571520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75483102-C-A

219571520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75483102-C-T

219571525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75483107-T-A

219571525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75483107-T-C

219571631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75483214-A-G

http://identifiers.org/hco/2/GRCh38#219571641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#75483224-C-A

219571641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75483224-C-T