42025708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100518494-T-C

42025749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100518532-A-G

http://identifiers.org/hco/17/GRCh38#42025848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100518601-C-A

42026381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519069-G-A

42026381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519069-G-T

42026554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519338-G-A

42026586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519367-C-T

http://identifiers.org/hco/17/GRCh38#42026686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100519471-C-A

42026686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519471-C-T

42026791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519576-T-C

42026791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100519576-T-G

http://identifiers.org/hco/17/GRCh38#42027001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100519762-C-A

42027001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100519762-C-T

http://identifiers.org/hco/17/GRCh38#42027229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100519987-C-A

42027229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100519987-C-T

http://identifiers.org/hco/17/GRCh38#42027280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520035-C-A

42027280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100520035-C-G

42027346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100520102-G-A

42027530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100520286-G-A

42027530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100520286-G-C

42027530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100520286-G-T

http://identifiers.org/hco/17/GRCh38#42027661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520407-C-A

42027661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100520407-C-T

42027695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100520441-C-T

42027787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520536-A-T

42027821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520576-G-A

42027821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520576-G-T

42027823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520578-T-C

http://identifiers.org/hco/17/GRCh38#42027824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520579-C-A

42027824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520579-C-T

http://identifiers.org/hco/17/GRCh38#42027834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520589-A-C

42027854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520609-C-T

42027863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520614-G-A

42027863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520614-G-T

42027891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520626-T-C

http://identifiers.org/hco/17/GRCh38#42027996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520667-C-A

42027996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520667-C-G

42027996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520667-C-T

http://identifiers.org/hco/17/GRCh38#42027997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100520668-C-A

42027997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520668-C-T

42028035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100520702-C-G

42028187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100520854-G-A

42028281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100520945-G-T

42028358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100520990-T-A

42028370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521002-G-A

42028370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521002-G-T

42028374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521008-T-A

42028374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521008-T-C

42028446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521091-C-T

42028619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100521220-G-A

42028619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100521220-G-T

42028620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100521221-T-A

42028620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100521221-T-C

42028649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100521250-G-T

42028770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521301-T-A

42028770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521301-T-C

42028811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100521342-C-T

42028847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100521378-G-A

http://identifiers.org/hco/17/GRCh38#42028859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100521390-A-C

42028875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100521406-C-T

http://identifiers.org/hco/17/GRCh38#42028891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100521422-C-A

42028891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100521422-C-G

42028891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100521422-C-T

42028970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100521501-T-A

42028970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100521501-T-C

42029012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100521564-G-A

42029012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: stop gained
orthologous variants: 100521564-G-T

42029091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521632-G-A

http://identifiers.org/hco/17/GRCh38#42029105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100521646-A-C

42029105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521646-A-G

42029105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521646-A-T

42029193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100521744-C-T

42031540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100523438-T-A

42031540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100523438-T-C

42031561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100523473-C-T

42031652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100523553-C-T

http://identifiers.org/hco/17/GRCh38#42031858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#100523755-C-A

42031858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100523755-C-G

42031858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100523755-C-T

http://identifiers.org/hco/17/GRCh38#42031881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100523798-C-A

42032274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524225-A-G

42032350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524287-C-T

42033075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524580-C-T

42033208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524692-C-T

42033223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524708-C-T

42033333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100524765-G-T

42033545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525002-G-A

42033683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525153-G-A

42034005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525322-C-T

http://identifiers.org/hco/17/GRCh38#42034169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100525424-C-A

42034169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525424-C-T

http://identifiers.org/hco/17/GRCh38#42034189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100525449-C-A

42034189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525449-C-T

http://identifiers.org/hco/17/GRCh38#42034190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100525450-C-A

42034190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525450-C-G

42034190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525450-C-T

42034193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525453-T-A

42034193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100525453-T-C

42034264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100525512-G-A

42034264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: missense variant
orthologous variants: 100525512-G-T

42034288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100525536-G-A

42034291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: synonymous variant
orthologous variants: 100525539-G-A

42036868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100527040-G-A

42036906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100527085-T-A

42036924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100527102-T-C

42037080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100527273-T-C

42037711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528544-C-G

42037711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528544-C-T

http://identifiers.org/hco/17/GRCh38#42037715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528548-C-A

42037715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528548-C-T

http://identifiers.org/hco/17/GRCh38#42037727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528560-C-A

42037727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528560-C-T

42037833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100528666-G-A

42037833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100528666-G-T

http://identifiers.org/hco/17/GRCh38#42037878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528711-C-A

42037878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100528711-C-T

42037881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 100528714-G-A

42037881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 100528714-G-T

42037949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528793-A-G

42037949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528793-A-T

42037950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528794-G-T

42037989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528810-T-C

http://identifiers.org/hco/17/GRCh38#42038003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528824-C-A

42038003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528824-C-T

42038008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528829-T-A

42038008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528829-T-C

42038072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528852-G-C

42038072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528852-G-T

http://identifiers.org/hco/17/GRCh38#42038083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528863-C-A

42038083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528863-C-T

42038096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528876-G-A

42038096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528876-G-C

42038188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528979-G-A

42038188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528979-G-T

http://identifiers.org/hco/17/GRCh38#42038210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100528995-A-C

42038210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100528995-A-G

42038277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100529068-G-T

42038317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100529104-C-T

http://identifiers.org/hco/17/GRCh38#42038332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100529120-C-A

http://identifiers.org/hco/17/GRCh38#42038436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100529638-C-A

42038503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100529704-A-G

42038738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530115-G-T

42038859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530234-G-T

http://identifiers.org/hco/17/GRCh38#42038942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530312-C-A

42039410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530527-G-C

http://identifiers.org/hco/17/GRCh38#42039449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530560-C-A

42039464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530572-G-A

42039464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530572-G-T

http://identifiers.org/hco/17/GRCh38#42039471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530579-C-A

42039497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530609-C-T

42039595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530661-T-A

42039595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530661-T-C

42039625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530690-G-A

42039625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530690-G-C

42039625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530690-G-T

42039634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530699-G-C

42039634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530699-G-T

http://identifiers.org/hco/17/GRCh38#42039657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530724-C-A

42039657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530724-C-G

42039657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100530724-C-T

http://identifiers.org/hco/17/GRCh38#42039738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530802-C-A

42039738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530802-C-G

http://identifiers.org/hco/17/GRCh38#42039764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100530827-C-A

42039764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530827-C-T

42039790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530862-G-A

42039790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530862-G-T

42039805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530877-G-A

42039805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100530877-G-T

42039957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531023-C-T

http://identifiers.org/hco/17/GRCh38#42039963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100531029-C-A

42039963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531029-C-T

42040069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531093-T-C

42040171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531153-A-G

42040195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531171-G-A

42040201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531177-A-G

42040242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531218-G-A

42040242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531218-G-T

42040337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531315-T-C

42040337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531315-T-G

42040372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531356-A-G

42040383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531367-G-A

42040383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531367-G-C

http://identifiers.org/hco/17/GRCh38#42040395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100531379-A-C

42040395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531379-A-G

42040433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531394-C-T

42040456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531417-G-A

42040456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531417-G-T

42040474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531435-G-A

42040474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531435-G-T

http://identifiers.org/hco/17/GRCh38#42040521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100531476-C-A

42040607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531541-C-T

42040614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531548-G-A

42040614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531548-G-T

42040616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531550-G-A

42040616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531550-G-T

42040693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531617-G-A

42040693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531617-G-C

42040717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531641-A-G

http://identifiers.org/hco/17/GRCh38#42040731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100531655-C-A

http://identifiers.org/hco/17/GRCh38#42040818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100531737-C-A

42040818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531737-C-T

42040837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531756-G-C

42040851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531770-C-T

42040937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100531857-G-A

42040964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, stop_gained
orthologous variants: 100531884-G-A

42040964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531884-G-C

42040964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531884-G-T

42041078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100531971-C-T

42041210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532017-A-G

42041225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532032-G-A

42041225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532032-G-T

42041776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532361-C-T

42041792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532383-A-G

42041854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100532443-A-G

42042627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533236-G-A

http://identifiers.org/hco/17/GRCh38#42042663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533277-C-A

42042684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533298-C-T

42042688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533302-G-A

42042688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533302-G-T

42042736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533353-A-G

42042736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533353-A-T

http://identifiers.org/hco/17/GRCh38#42042774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533391-C-A

42042774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533391-C-T

42042776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533393-G-A

42042776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533393-G-C

42042776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533393-G-T

http://identifiers.org/hco/17/GRCh38#42042798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533415-C-A

42042822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533438-G-A

42042822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100533438-G-T

http://identifiers.org/hco/17/GRCh38#42042827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533443-C-A

42042827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 100533443-C-T

http://identifiers.org/hco/17/GRCh38#42042850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533466-C-A

42042850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533466-C-T

http://identifiers.org/hco/17/GRCh38#42042852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533468-C-A

42042852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533468-C-T

42042890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533506-G-T

42042904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533520-T-C

http://identifiers.org/hco/17/GRCh38#42042924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533540-C-A

42042924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533540-C-T

42042938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533554-G-A

42042938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533554-G-T

42042966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533582-G-A

42042966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, stop_gained
orthologous variants: 100533582-G-T

http://identifiers.org/hco/17/GRCh38#42043023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533638-C-A

42043023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533638-C-T

42043053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533668-G-A

42043076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, stop_gained
orthologous variants: 100533691-G-A

http://identifiers.org/hco/17/GRCh38#42043205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100533775-C-A

42043205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533775-C-T

42043206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100533776-A-G

42043206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533776-A-T

42043264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533834-T-C

42043265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533835-A-G

42043297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, stop_gained
orthologous variants: 100533867-C-T

42043369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533936-G-A

42043370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533937-G-A

42043370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant
orthologous variants: 100533937-G-T

http://identifiers.org/hco/17/GRCh38#42043440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534038-C-A

42043440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534038-C-G

42043468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534067-G-A

42043470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534068-G-A

42043470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534068-G-T

http://identifiers.org/hco/17/GRCh38#42043487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534085-C-A

42043487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534085-C-T

42043493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534091-G-A

42043493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534091-G-T

42043523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534122-T-C

42043558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100534159-G-A

42043565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100534166-T-C

http://identifiers.org/hco/17/GRCh38#42043580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534181-C-A

42043580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534181-C-T

http://identifiers.org/hco/17/GRCh38#42043581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534182-A-C

42043581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534182-A-G

42043612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534186-G-A

42043612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534186-G-T

42043627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534201-G-A

42043627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534201-G-C

http://identifiers.org/hco/17/GRCh38#42043628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534202-A-C

42043628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534202-A-G

42043628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534202-A-T

http://identifiers.org/hco/17/GRCh38#42043648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100534221-C-A

42043692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100534250-A-G

42049532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100536203-C-T

42049652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100536319-G-T

42050481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100537121-G-A

42050481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100537121-G-C

42050481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100537121-G-T

http://identifiers.org/hco/17/GRCh38#42050535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537168-C-A

42050535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 100537168-C-G

42050535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 100537168-C-T

42050536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 100537169-G-A

42050536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 100537169-G-T

http://identifiers.org/hco/17/GRCh38#42050539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537172-C-A

http://identifiers.org/hco/17/GRCh38#42050552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537185-C-A

42050597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100537222-G-A

42050597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100537222-G-T

42050602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100537227-G-A

http://identifiers.org/hco/17/GRCh38#42050605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537230-C-A

http://identifiers.org/hco/17/GRCh38#42050617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537242-C-A

42050620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100537245-G-T

42050665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100537290-G-A

42050665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100537290-G-T

http://identifiers.org/hco/17/GRCh38#42050673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#100537298-C-A

42050673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100537298-C-T

42050729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100537340-C-T

42050770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100537348-C-T

42050801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100537368-C-G

42050801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100537368-C-T

42051645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100538493-G-A

42051702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100538550-A-G

42052207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100538975-G-T

42052216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100538984-G-A

42052216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100538984-G-C

42052423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539167-A-G

42052589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539289-G-A

42052667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539329-A-G

42052794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539449-G-A

42052807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539462-G-A

42052878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539488-G-A

42052893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539503-G-A

42052914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539526-T-C

42052917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100539529-A-G

42053066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100540219-G-A

42053071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100540222-G-T

42053360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100540890-C-T

42053578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541081-C-T

42053645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541133-C-T

42053738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541213-G-A

42053774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541247-G-A

42053892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541369-G-A

42053926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541403-G-C

42053933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541408-T-A

42054086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541542-T-C

42054553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541886-G-A

42054557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100541890-G-A

http://identifiers.org/hco/17/GRCh38#42054905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100541982-C-A

42055151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542227-T-C

42055198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542279-C-T

42055367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542430-T-C

42055635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542679-C-T

42055654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542698-C-T

42055805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542842-C-T

42055892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100542909-G-A

42058108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100544490-G-C

42058114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100544496-A-T

42058367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100544744-G-A

42059096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545042-A-G

42059119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545065-T-C

42059183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545128-C-T

42059198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545136-C-T

42059223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545171-C-T

42059299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545246-G-A

42059372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545316-T-C

42059475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545426-G-A

42059475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100545426-G-T

42061410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546839-G-A

42061410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546839-G-C

42061410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546839-G-T

42061441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546870-A-G

42061448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546877-T-C

http://identifiers.org/hco/17/GRCh38#42061451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100546880-C-A

42061489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546898-A-G

42061490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546899-G-T

42061491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546900-G-T

http://identifiers.org/hco/17/GRCh38#42061514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100546922-C-A

42061514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546922-C-G

42061514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546922-C-T

42061552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546976-T-C

http://identifiers.org/hco/17/GRCh38#42061569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100546993-C-A

42061569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100546993-C-T

http://identifiers.org/hco/17/GRCh38#42061590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547008-C-A

42061590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547008-C-T

42061609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547025-T-C

42061615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547032-G-A

42061615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547032-G-T

http://identifiers.org/hco/17/GRCh38#42061654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547069-C-A

http://identifiers.org/hco/17/GRCh38#42061664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547079-C-A

42061664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547079-C-G

42061666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547081-G-A

http://identifiers.org/hco/17/GRCh38#42061702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547117-C-A

http://identifiers.org/hco/17/GRCh38#42061732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547139-C-A

42061732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547139-C-G

42061732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547139-C-T

42061750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547152-G-A

42062055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547284-G-A

42062055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547284-G-T

42062061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547290-T-C

http://identifiers.org/hco/17/GRCh38#42062110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547333-C-A

42062110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547333-C-T

42062278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547479-G-T

http://identifiers.org/hco/17/GRCh38#42062306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547541-C-A

42062306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547541-C-T

42062315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547550-G-T

42062427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547655-A-G

http://identifiers.org/hco/17/GRCh38#42062531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100547709-C-A

42062586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547766-A-G

42062586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547766-A-T

42062605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547785-A-G

42062644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547823-T-C

42062644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100547823-T-G

http://identifiers.org/hco/17/GRCh38#42062750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100548150-C-A

42062750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100548150-C-G

42062750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100548150-C-T

42062834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100548228-T-C

http://identifiers.org/hco/17/GRCh38#42062862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100548256-C-A

42062862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100548256-C-T

42062922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100548316-A-G

42063012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100548406-G-A

42063012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100548406-G-T

42063669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100548651-C-T

42063911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100548891-C-T

42064366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100549439-C-T

42064625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100549716-T-G

42065300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100550531-G-A

42065300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100550531-G-T

42065345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100550578-G-C

42065437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100550670-G-A

42065437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100550670-G-T

42065475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100550708-A-G

42065475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100550708-A-T

42066581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100551083-G-A

42066620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100551117-G-A

42066620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100551117-G-C

42067323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100551869-C-G

42067520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100552052-G-A

42067796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100552313-G-A

42067796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100552313-G-C

42067934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100552439-G-A

42068214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100552717-C-T

42068267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100552821-G-A

42068267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100552821-G-T

42068657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100560767-G-C

42068701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100560816-T-G

42068714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100560828-C-T

http://identifiers.org/hco/17/GRCh38#42068876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100560963-A-C

42068945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561030-G-A

42068945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561030-G-C

42069007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561092-G-A

42069081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561146-G-C

42069081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561146-G-T

42069109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561172-C-T

42069139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561202-G-A

42069279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561297-G-A

42069279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561297-G-C

http://identifiers.org/hco/17/GRCh38#42069482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100561560-C-A

42069535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100561597-G-C

42071406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563201-T-C

42071865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563632-C-T

42071866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563633-G-A

42071986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563741-C-T

42072324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563876-C-T

42072346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100563889-C-T

42072556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564074-G-T

42073543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564487-G-A

42073698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564550-G-A

42073845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564657-C-G

42073931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564739-C-T

42073952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564762-G-A

42073968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100564778-C-T

42074833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100565306-C-T

42075062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100565535-A-G

42075329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100565758-A-G

42075721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100565959-C-T

42076050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566138-C-G

42076050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566138-C-T

42076069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566156-G-C

42076262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566344-C-G

42076579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566689-G-A

42076877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566974-G-A

42076898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100566987-C-T

42077334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100567361-T-G

http://identifiers.org/hco/17/GRCh38#42077527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100567514-C-A

42077800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100568251-C-T

42078239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100568666-G-A

42078252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100568677-G-A

42078672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100569078-G-A

42078771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100569163-C-T

42078855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569226-G-A

42079797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569421-A-G

42079960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569579-G-A

42080103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569720-C-T

42080136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569754-G-A

42080136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569754-G-T

42080162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100569780-G-C

42080725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100570336-G-A

42080763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100570364-C-T

42080807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100570408-C-G

42080807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100570408-C-T

42089220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100573941-G-A

42089226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100573947-G-A

42089242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100573973-G-A

42089413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100574158-A-G

42090028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: -C-T

42090232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: -C-T

42091657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100576520-C-G

42091778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100576646-T-A

http://identifiers.org/hco/17/GRCh38#42092043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100577063-C-A

42092079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100577099-C-G

42092079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100577099-C-T

42092262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100577437-A-G

42092270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100577445-A-G

http://identifiers.org/hco/17/GRCh38#42092562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100577827-A-C

42092769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100577979-C-T

http://identifiers.org/hco/17/GRCh38#42092775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100577985-C-A

42092833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578017-C-T

42092930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578079-C-G

42092930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578079-C-T

http://identifiers.org/hco/17/GRCh38#42092939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100578086-C-A

42093212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578342-C-T

42093237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578367-C-G

42093237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578367-C-T

http://identifiers.org/hco/17/GRCh38#42093302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100578432-C-A

42093423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578530-G-A

42093429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578536-G-A

42093439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100578545-C-T

42094740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100579203-G-T

42094890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100579363-G-T

42094917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100579389-C-T

42095861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100580372-T-C

42096089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581041-C-T

42096128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581091-C-T

42096134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581100-G-A

42096168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581122-A-G

42096382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581212-C-T

42096482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581296-C-T

42096934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581694-G-A

http://identifiers.org/hco/17/GRCh38#42097103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100581830-C-A

42097103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581830-C-G

42097115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581842-C-T

42097126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100581852-T-A

42097363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: 100582313-T-G

http://identifiers.org/hco/17/GRCh38#42097561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#100582516-A-C

42098344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100583179-G-A

42098344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100583179-G-C

42098344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33722
most severe consequence: intron_variant, undefined
orthologous variants: 100583179-G-T