http://identifiers.org/hco/1/GRCh38#90916413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106765725-A-C

90916413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106765725-A-T

90916496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106765801-G-T

90916666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106765966-T-C

90916831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106766135-T-C

90917017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106766329-C-T

90917066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106766375-A-G

90917150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106766504-C-T

90918088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106767442-G-A

http://identifiers.org/hco/1/GRCh38#90918185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106767536-C-A

90918267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106767604-G-A

90918267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106767604-G-T

90918489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106767754-G-A

90918489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106767754-G-T

90919355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106768472-G-A

90919877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106768998-T-C

90919891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106769011-T-C

90920415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106769490-G-C

90920831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106769851-G-C

http://identifiers.org/hco/1/GRCh38#90920970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106769978-C-A

90921049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106770050-C-T

90921782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106770443-T-C

90921797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106770453-T-C

90922232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106770828-C-T

90922552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106772992-G-A

90922901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773052-G-A

90923078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773211-T-C

90923108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773229-A-G

90923133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773254-G-A

90923133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773254-G-T

90923191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773300-G-A

90923245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773352-T-G

90923274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773384-G-A

90923290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773400-T-C

90923299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773409-T-C

90923317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773427-G-A

90923383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773467-T-C

90923450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773508-C-T

90923540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773581-T-C

90923585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106773736-C-T

90924229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106774074-C-T

90924418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106774270-G-A

90924837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106774650-G-A

http://identifiers.org/hco/1/GRCh38#90926830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106775550-C-A

90927035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106775904-A-G

90929580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106777067-G-A

90929819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106777292-C-T

90930305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106777478-T-C

90930565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106777725-G-C

90930669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106777823-A-T

90932195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106778035-C-T

90932524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106778693-G-A

90932952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779022-T-C

90932973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779044-T-C

90933274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779319-A-G

90933294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779339-G-A

90933990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779641-G-A

90933990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106779641-G-C

90934505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780090-T-C

90934515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780100-C-G

90934573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780157-C-T

90934574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780158-G-A

90935368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780752-T-C

90935368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780752-T-G

http://identifiers.org/hco/1/GRCh38#90935487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106780870-C-A

90935487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106780870-C-T

90935602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106780986-A-G

http://identifiers.org/hco/1/GRCh38#90935655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106781038-C-A

90935655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106781038-C-T

90936262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106781590-T-C

90936354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106781653-G-C

90936354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106781653-G-T

90936883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106782139-C-T

90936901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106782154-T-C

90937013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106782265-G-A

90937227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106782470-T-C

90937494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106782706-T-C

90937660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106782872-G-A

90937779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106782991-G-C

90937779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106782991-G-T

90937784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106782996-T-C

90938202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106783406-A-G

90938411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783615-A-G

90938453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783657-G-A

http://identifiers.org/hco/1/GRCh38#90938522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106783726-A-C

90938522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783726-A-G

90938552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783756-A-G

90938555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783759-T-A

90938555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783759-T-G

90938597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106783801-T-C

90939144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784333-T-C

90939254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106784443-A-G

90939335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106784524-A-G

90939442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784631-C-T

90939446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106784635-A-G

90939493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784682-G-A

http://identifiers.org/hco/1/GRCh38#90939536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106784725-C-A

90939536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784725-C-G

90939536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106784725-C-T

90939540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784729-G-A

90939540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106784729-G-C

http://identifiers.org/hco/1/GRCh38#90939848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106785037-C-A

http://identifiers.org/hco/1/GRCh38#90939875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106785064-A-C

90939911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785100-A-T

90939950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785139-A-G

90939950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785139-A-T

90940034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785223-G-A

90940302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106785491-T-G

90940331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785520-T-C

90940331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785520-T-G

90940358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785547-T-C

90940367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106785556-A-G

90940647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106785839-T-C

90940804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106785996-C-T

90941120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106786312-C-T

http://identifiers.org/hco/1/GRCh38#90941224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106786416-C-A

90941303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106786495-A-G

90941304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106786496-T-C

90941304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106786496-T-G

http://identifiers.org/hco/1/GRCh38#90941325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106786517-A-C

90941412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106786601-C-T

90941799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106786923-T-C

90942013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106787144-A-G

90942161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106787245-A-G

90942679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106787684-C-T

90943700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106788142-T-A

90943927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106788334-G-A

90945369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106789809-A-G

90946140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106790550-T-C

90946379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106790770-T-C

90946551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106791125-C-T

90960514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106793909-C-T

90960725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106794117-C-G

http://identifiers.org/hco/1/GRCh38#90960784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106794166-A-C

90960877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106794238-T-C

90961045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106794341-A-T

90961326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106794663-T-C

90961573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106794932-T-C

90961910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795229-C-T

90962075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795338-G-A

90962303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795562-A-G

90962338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795594-C-T

90962354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795610-T-C

90962620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106795806-C-T

http://identifiers.org/hco/1/GRCh38#90962687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106795870-A-C

90963110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106796230-A-G

90963132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106796251-G-T

90964211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797112-T-C

90964340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797231-T-C

90964340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797231-T-G

90964341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797232-C-T

90964499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797380-A-G

90964952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797756-C-T

90965039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797823-C-G

90965223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797952-G-A

90965233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797962-G-T

90965274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797979-G-A

90965274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106797979-G-C

90965307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106798013-T-C

90965557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106798255-T-C

90967173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106799905-C-T

90967453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800174-G-C

http://identifiers.org/hco/1/GRCh38#90967477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106800186-C-A

90967521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800228-C-T

90967688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800342-G-A

90967738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800388-G-A

90968658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800912-A-T

90968684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106800942-A-T

90969022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106801291-A-G

90969047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106801315-T-C

http://identifiers.org/hco/1/GRCh38#90971031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106803537-C-A

90971066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106803597-G-A

http://identifiers.org/hco/1/GRCh38#90971296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106803832-C-A

http://identifiers.org/hco/1/GRCh38#90971321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106803857-C-A

90971321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106803857-C-T

90974860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106809930-C-T

http://identifiers.org/hco/1/GRCh38#90974876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106809947-C-A

90974876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106809947-C-T

90975209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106810389-C-T

90979114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106811846-G-A

90980008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106812316-T-C

90981845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106814226-C-T

90982129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106814477-T-A

90982138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106814486-T-C

90982185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106814531-T-C

90982480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106814819-T-C

91008659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106831522-C-G

91009272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106831679-T-G

91009424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106831816-T-A

91009514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106832023-T-C

91009670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106832155-A-G

91010129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106833408-T-C

91010161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106833448-A-G

91010231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106833515-T-G

91011155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106834696-T-C

91011703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106835443-G-A

91012079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106835804-T-C

91012111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106835839-G-T

91013702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106836910-T-C

91013705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106836913-T-C

91014082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106837360-G-A

91014093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106837371-T-C

91014491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106838075-T-A

91014755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106838335-G-A

91014860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106838427-T-C

91015672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839540-G-C

91015712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839578-T-C

91015712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839578-T-G

91015810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839675-G-C

91016007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839794-C-T

91016079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106839874-T-C

91018183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841088-A-T

91018515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841355-A-G

91018546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841382-A-T

91018580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841411-A-G

http://identifiers.org/hco/1/GRCh38#91019225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106841901-A-C

91019286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841954-C-T

91019308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106841979-A-G

91019426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106842080-T-C

91019913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106842184-C-T

91019923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106842195-T-A

91019963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106842234-C-T

91020144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106842371-T-C

91020572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106842929-G-A

91021249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106843614-A-G

91021392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106843788-A-G

91021414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106843810-C-T

http://identifiers.org/hco/1/GRCh38#91021468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106843870-C-A

91021468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106843870-C-T

91021634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106844042-G-C

http://identifiers.org/hco/1/GRCh38#91021763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106844165-C-A

91021763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844165-C-T

http://identifiers.org/hco/1/GRCh38#91021908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106844313-C-A

91021908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844313-C-T

91021966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844372-G-A

91021966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844372-G-C

91021966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844372-G-T

91021980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106844388-T-C

91022027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106844435-G-A

91022027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106844435-G-T

91022082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5 prime UTR variant
orthologous variants: 106844490-G-A

91022082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5 prime UTR variant
orthologous variants: 106844490-G-C

91022116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5 prime UTR variant
orthologous variants: 106844523-C-G

91022116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29222
most severe consequence: 5 prime UTR variant
orthologous variants: 106844523-C-T