4182695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 81463562-G-A

4182695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 81463562-G-C

4182695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 81463562-G-T

http://identifiers.org/hco/19/GRCh38#4182696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#81463563-A-C

4182696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 81463563-A-G

4182741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: splice_donor_variant, undefined
orthologous variants: 81463603-G-A

4182741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: splice_donor_variant, undefined
orthologous variants: 81463603-G-C

4182741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: splice_donor_variant, undefined
orthologous variants: 81463603-G-T

4182771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81463624-G-A

4182771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81463624-G-T

http://identifiers.org/hco/19/GRCh38#4184175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81464356-C-A

4184175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464356-C-T

4184176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464357-G-A

4184177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464358-G-A

4184177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464358-G-C

4184178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464359-C-G

4184532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464625-C-T

4184776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81464819-G-C

4184785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81464828-A-G

4184793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464836-G-A

4184820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464840-G-T

4184843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464863-T-G

4184856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464876-G-C

4184860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464880-A-G

4184876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464888-G-A

4184887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464899-A-G

4184924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464936-A-G

4184934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464946-C-G

4184935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464947-C-G

4184935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464947-C-T

4184936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464948-A-G

4184948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464960-G-A

4184948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464960-G-C

4184952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464964-G-A

4184960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464972-A-G

4184972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464984-G-A

4184984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464996-G-A

4184986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81464998-G-A

4184996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465008-A-G

4185850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465123-G-T

4185895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465170-T-G

http://identifiers.org/hco/19/GRCh38#4186134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81465341-C-A

4186134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465341-C-T

4186196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465392-G-A

http://identifiers.org/hco/19/GRCh38#4186333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81465478-C-A

4186333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81465478-C-T

4186341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81465486-C-G

4186412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 81465527-A-G

4186602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81465721-T-G

4186648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465771-G-C

4186684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81465813-G-A

4186684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81465813-G-C

4186754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81465914-C-T

http://identifiers.org/hco/19/GRCh38#4187018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81466160-A-C

4187058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81466200-T-G

4187238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81466365-C-T

4187286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81466388-A-G

4187392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81466482-A-G

4187409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81466499-T-A

4191094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81467256-C-T

4197730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81468886-C-T

4197954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81469121-C-T

4198052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, undefined
orthologous variants: 81469228-G-T

4198273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, missense_variant
orthologous variants: 81469431-T-A

4198273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, missense_variant
orthologous variants: 81469431-T-C

4198277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81469435-T-G

4198505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 81469562-G-A

4198505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 81469562-G-T

4199614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81470435-T-A

4199614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81470435-T-C

4199628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81470449-G-T

4199742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 81470560-G-A

4199742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 81470560-G-T

http://identifiers.org/hco/19/GRCh38#4199779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81470597-C-A

4199779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81470597-C-T

http://identifiers.org/hco/19/GRCh38#4199851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#81470674-C-A

4199851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81470674-C-G

4199851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81470674-C-T

http://identifiers.org/hco/19/GRCh38#4200146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81470967-C-A

4200146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 81470967-C-T

4200150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81470971-G-A

4200150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81470971-G-T

4200183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81471004-T-C

http://identifiers.org/hco/19/GRCh38#4200187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81471011-C-A

4200187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81471011-C-T

http://identifiers.org/hco/19/GRCh38#4202057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#81471553-C-A

4202057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 81471553-C-T

http://identifiers.org/hco/19/GRCh38#4202133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81471609-A-C

4202133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81471609-A-G

4202655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472000-C-T

http://identifiers.org/hco/19/GRCh38#4202674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81472022-C-A

4202674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472022-C-T

4202710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472052-A-G

http://identifiers.org/hco/19/GRCh38#4202725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81472066-C-A

4202725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472066-C-T

4202769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472115-A-G

4202769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472115-A-T

http://identifiers.org/hco/19/GRCh38#4202855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81472190-C-A

4202855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81472190-C-T

4207346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474014-A-G

4207363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81474031-C-T

4207376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474043-G-A

4207376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474043-G-C

4207401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474069-T-G

4207413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474070-A-G

4207478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474089-G-A

4207478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474089-G-T

4207688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474297-C-T

4207720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81474333-G-T

4207937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81474551-A-G

http://identifiers.org/hco/19/GRCh38#4208049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81474651-C-A

4208049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81474651-C-G

4208099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81474691-T-C

4208099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81474691-T-G

http://identifiers.org/hco/19/GRCh38#4208217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81474794-C-A

4208217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81474794-C-T

http://identifiers.org/hco/19/GRCh38#4208688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81475045-C-A

http://identifiers.org/hco/19/GRCh38#4208723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81475101-C-A

4208724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81475102-T-G

http://identifiers.org/hco/19/GRCh38#4208908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81475256-C-A

http://identifiers.org/hco/19/GRCh38#4208979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81475337-A-C

4208979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81475337-A-G

4208979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81475337-A-T

4210168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475788-C-T

4210327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81475924-G-T

4210447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476026-T-C

4210447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476026-T-G

http://identifiers.org/hco/19/GRCh38#4210454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476034-A-C

4210454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476034-A-G

4210454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476034-A-T

4210465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476045-T-A

4210465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476045-T-C

http://identifiers.org/hco/19/GRCh38#4210470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476050-C-A

4210470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476050-C-G

4210470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476050-C-T

http://identifiers.org/hco/19/GRCh38#4210609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476190-C-A

4210609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81476190-C-T

4210622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81476202-T-A

4212290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476409-G-A

4212310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476430-C-T

http://identifiers.org/hco/19/GRCh38#4212325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476450-A-C

4212325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476450-A-G

4212325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476450-A-T

http://identifiers.org/hco/19/GRCh38#4212328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476453-A-C

4212328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476453-A-G

4212328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476453-A-T

4212332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476457-A-G

4212332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476457-A-T

http://identifiers.org/hco/19/GRCh38#4212411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476555-C-A

4212411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476555-C-T

4212426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476567-G-A

4212426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476567-G-C

4212426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476567-G-T

4212427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476568-G-A

4212427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476568-G-C

4212427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476568-G-T

http://identifiers.org/hco/19/GRCh38#4212446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81476583-C-A

4212446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476583-C-T

4212521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81476654-G-A

4212521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81476654-G-C

4212521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81476654-G-T

4212551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476696-G-A

4212551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476696-G-C

4212647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81476773-G-A

http://identifiers.org/hco/19/GRCh38#4216056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81477888-C-A

4216056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477888-C-T

4216164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478022-G-A

4216164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478022-G-T

4216175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478033-T-C

http://identifiers.org/hco/19/GRCh38#4216229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81478071-C-A

4216460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478292-A-G

4216460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478292-A-T

http://identifiers.org/hco/19/GRCh38#4216578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81478379-C-A

4216685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81478486-G-A

4216685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81478486-G-T

4216801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81478608-T-C

http://identifiers.org/hco/19/GRCh38#4216824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81478631-A-C

http://identifiers.org/hco/19/GRCh38#4217007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81478997-C-A

4217007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81478997-C-G

http://identifiers.org/hco/19/GRCh38#4217101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81479088-A-C

4217101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479088-A-G

4217152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479108-C-G

4217163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479114-G-C

4217215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479166-A-G

4217298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479279-G-C

4217399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479374-C-T

4217677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479406-G-A

4217677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479406-G-T

4217686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479415-G-A

4217686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479415-G-C

4217686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479415-G-T

4217689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479418-G-A

4217689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479418-G-T

http://identifiers.org/hco/19/GRCh38#4217746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81479475-C-A

4217746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479475-C-G

4217746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479475-C-T

4217803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479532-T-A

4217803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479532-T-C

http://identifiers.org/hco/19/GRCh38#4217810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81479539-C-A

4217810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479539-C-G

4217810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: stop gained
orthologous variants: 81479539-C-T

http://identifiers.org/hco/19/GRCh38#4217921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81479562-C-A

4217921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479562-C-G

4217921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479562-C-T

http://identifiers.org/hco/19/GRCh38#4218048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81479607-C-A

4218048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479607-C-T

4218085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81479649-G-A

4218085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479649-G-C

4218085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81479649-G-T

4219875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81481086-G-T

4222623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482090-C-T

4222643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482107-G-T

4222717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81482186-G-A

4222801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482273-G-T

4222873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482329-G-A

4222873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482329-G-T

http://identifiers.org/hco/19/GRCh38#4222895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81482350-C-A

4222895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482350-C-G

4222895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482350-C-T

4224106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482603-G-A

4224106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482603-G-T

4224114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482614-C-G

4224114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482614-C-T

4224141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81482641-C-T

4224147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: synonymous variant
orthologous variants: 81482647-C-T

4224213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482713-G-T

4224251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482750-A-G

http://identifiers.org/hco/19/GRCh38#4224253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81482752-C-A

4224253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482752-C-T

4224302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482785-G-A

http://identifiers.org/hco/19/GRCh38#4224306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#81482789-C-A

4224306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482789-C-T

4224384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: intron variant
orthologous variants: 81482880-A-G

4224469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29424
most severe consequence: missense variant
orthologous variants: 81482975-T-G