27496840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31454899-T-C

http://identifiers.org/hco/2/GRCh38#27496846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31454905-C-A

27496851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31454910-G-A

27496880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31454939-A-G

27496955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31455014-C-T

http://identifiers.org/hco/2/GRCh38#27496980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31455039-C-A

27496980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455039-C-T

27497012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455119-A-G

27497013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455120-T-C

http://identifiers.org/hco/2/GRCh38#27497022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31455156-C-A

27497022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455156-C-T

http://identifiers.org/hco/2/GRCh38#27497033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31455206-C-A

27497033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455206-C-G

27497033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455206-C-T

27497057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455282-T-C

http://identifiers.org/hco/2/GRCh38#27497080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31455305-C-A

27497081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455306-T-C

27497084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455309-T-C

27497163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455433-G-A

27497199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455469-G-A

27497199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31455469-G-T

http://identifiers.org/hco/2/GRCh38#27497494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31455750-C-A

27497539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456035-T-C

27497689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456192-A-G

27497842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456538-T-C

27498143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456845-G-A

27498143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456845-G-C

27498155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456857-G-A

27498155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456857-G-T

27498317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31456964-C-G

27498317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31456964-C-T

http://identifiers.org/hco/2/GRCh38#27498352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31456998-C-A

27498352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31456998-C-T

http://identifiers.org/hco/2/GRCh38#27498353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31456999-C-A

27498396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457040-A-G

http://identifiers.org/hco/2/GRCh38#27498460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31457085-C-A

27498460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457085-C-G

27498474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457099-T-C

27498557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457181-C-G

27498708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457328-T-A

27498708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457328-T-C

http://identifiers.org/hco/2/GRCh38#27498812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31457431-C-A

27498812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457431-C-T

27498879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457696-G-T

http://identifiers.org/hco/2/GRCh38#27498903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31457720-C-A

27498903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457720-C-T

27499073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457850-G-A

27499073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457850-G-C

27499073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457850-G-T

27499087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457864-G-A

27499087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457864-G-T

27499121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457898-A-G

27499263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458045-G-C

27499273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458055-G-A

27499322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458094-C-G

http://identifiers.org/hco/2/GRCh38#27499336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31458108-C-A

27499336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458108-C-T

http://identifiers.org/hco/2/GRCh38#27499471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31458230-A-C

http://identifiers.org/hco/2/GRCh38#27499478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31458237-C-A

27499478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458237-C-T

http://identifiers.org/hco/2/GRCh38#27499531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31458296-A-C

27499531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458296-A-G

27500999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459377-G-T

27501274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459643-G-A

27501276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459645-G-A

27501276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459645-G-T

27501280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459649-A-G

27501629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459988-G-T

27501631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459990-C-T

27501635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459994-T-A

27501635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459994-T-C

27501657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460013-T-C

27501657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460013-T-G

27502189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460514-G-C

27502581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460901-T-A

27502581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460901-T-C

27502581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460901-T-G

http://identifiers.org/hco/2/GRCh38#27502608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31460915-C-A

27502608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460915-C-T

http://identifiers.org/hco/2/GRCh38#27502635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31460942-A-C

27502641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460949-T-A

27502733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461505-C-G

27502733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461505-C-T

27502817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461587-C-G

27503083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461838-G-A

27503352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462162-C-T

27503401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462210-T-C

http://identifiers.org/hco/2/GRCh38#27503458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31462260-C-A

27503478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462280-G-T

27503493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462292-T-A

27503493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462292-T-C

http://identifiers.org/hco/2/GRCh38#27503541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31462340-A-C

http://identifiers.org/hco/2/GRCh38#27503604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31462403-C-A

27503604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31462403-C-G

27503604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31462403-C-T

27503636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462437-T-C

27503646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462443-T-C

27503751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462523-A-T

27503863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462642-G-C

27504125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462892-T-C

27504450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31463169-C-G

27504450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31463169-C-T

http://identifiers.org/hco/2/GRCh38#27504592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31463272-C-A

27504595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31463273-G-A

http://identifiers.org/hco/2/GRCh38#27505574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31463588-C-A

27505574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31463588-C-T

http://identifiers.org/hco/2/GRCh38#27505686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31463801-C-A

http://identifiers.org/hco/2/GRCh38#27505720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31463834-C-A

27505720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 31463834-C-T

27505807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31463921-T-C

27505858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31463972-G-C

27506157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464098-C-T

27506310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464209-G-C

27506355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464269-C-T

27506422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464349-A-G

27506455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464384-T-C

27506490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31464419-G-A

27506655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31464545-A-G

27506671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31464561-G-A

27506762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31464639-T-C

27506769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31464646-A-G

http://identifiers.org/hco/2/GRCh38#27506771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31464648-C-A

27506797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31464674-G-A

27506797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31464674-G-T

27506905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464782-G-A

27506987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464858-G-T

27507003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464873-A-G

http://identifiers.org/hco/2/GRCh38#27507118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31464995-C-A

27507118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464995-C-T

27507126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465003-G-A

27507126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465003-G-T

http://identifiers.org/hco/2/GRCh38#27507203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465067-C-A

27507203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465067-C-G

http://identifiers.org/hco/2/GRCh38#27507375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465234-A-C

27507375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465234-A-G

27507393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465252-G-A

27507393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465252-G-C

27507393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465252-G-T

http://identifiers.org/hco/2/GRCh38#27507420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465280-C-A

27507427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465287-G-T

http://identifiers.org/hco/2/GRCh38#27507470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465322-C-A

27507470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465322-C-T

http://identifiers.org/hco/2/GRCh38#27507507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465350-C-A

27507507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465350-C-T

http://identifiers.org/hco/2/GRCh38#27507565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465407-A-C

27507583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31465426-C-T

http://identifiers.org/hco/2/GRCh38#27507619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31465467-C-A

27507876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466082-G-A

27507895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466101-C-T

27507956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466159-G-A

http://identifiers.org/hco/2/GRCh38#27508027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31466230-A-C

27508027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31466230-A-G

http://identifiers.org/hco/2/GRCh38#27508028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31466231-A-C

27508056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31466259-C-T

27508143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466342-C-G

27508143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466342-C-T

27508156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466353-C-G

27508270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466468-T-C

http://identifiers.org/hco/2/GRCh38#27508291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31466479-C-A

27508328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466508-G-A

27508328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466508-G-T

27508548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466668-T-A

27508789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466693-A-G

27508862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466737-T-C

27508898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466769-G-T

27508933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466801-G-T

27509031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31466898-G-A

27509139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31467004-C-T

27515961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479375-G-A

27515961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479375-G-T

27516057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479490-G-A

27516073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479506-G-C

27516136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479561-C-G

27516150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479575-A-G

27516157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479582-T-G

27516296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31479653-T-G

27516791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31480051-G-A

27518946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31482074-A-G

27518946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31482074-A-T

http://identifiers.org/hco/2/GRCh38#27522297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483565-A-C

http://identifiers.org/hco/2/GRCh38#27522340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483592-C-A

27522340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483592-C-T

http://identifiers.org/hco/2/GRCh38#27522367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483619-C-A

27522367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483619-C-G

27522367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483619-C-T

27522381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483633-A-G

27522381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483633-A-T

27522382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483634-G-T

http://identifiers.org/hco/2/GRCh38#27522389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483641-C-A

27522389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483641-C-T

http://identifiers.org/hco/2/GRCh38#27522403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483655-C-A

27522403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483655-C-G

http://identifiers.org/hco/2/GRCh38#27522404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31483656-C-A

27522404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483656-C-T

27522477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31483718-C-T

27522519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31483760-T-C

27522519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31483760-T-G

27522537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31483778-T-G

27522636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483876-G-A

27522636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483876-G-T

27522682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483911-G-A

27522682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483911-G-C

27522682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31483911-G-T

27523256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31484258-C-G

27523256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: intron variant
orthologous variants: 31484258-C-T

27523310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31484312-G-A

27523310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31484312-G-T

27523370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31484372-T-C

27523370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31484372-T-G

27523385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: synonymous variant
orthologous variants: 31484387-A-G

27523404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31484406-G-A

27523404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31484406-G-T

http://identifiers.org/hco/2/GRCh38#27523407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31484409-C-A

27523407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: missense variant
orthologous variants: 31484409-C-T

27523455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 3 prime UTR variant
orthologous variants: 31484452-T-C

27523459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 3 prime UTR variant
orthologous variants: 31484456-T-A

http://identifiers.org/hco/2/GRCh38#27523482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31484473-C-A

27523482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4196
most severe consequence: 3 prime UTR variant
orthologous variants: 31484473-C-T